Template:Kyoto/Notebook/Magnetosome

From 2014.igem.org

(Difference between revisions)

Latest revision as of 03:52, 18 October 2014

7/15

Transformation

Tatsui, Matsumoto and Sukegawa

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_J23101(Pcon)	2	20(2/23)	22	LB(CP)
BBa_B0032(RBS)	2	20(2/23)	22	LB(CP)

7/16

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_B0030(1)	2	20(2/23)	22	LB(CP)
BBa_B0030(2)	2	20(bought)	22	LB(CP)
BBa_B0032(1)	2	20(2/23)	22	LB(CP)
BBa_B0032(2)	2	20(bought)	22	LB(CP)

7/17

Colony PCR

Tatsui, Matsumoto, Li, and Yamauchi

NameⅠ	NameⅡ
7/16 BBa_B0030(1) Colony_1	7/16 BBa_B0032(1) Colony_1
7/16 BBa_B0030(1) Colony_2	7/16 BBa_B0032(1) Colony_2
7/16 BBa_B0030(1) Colony_3	7/16 BBa_B0032(1) Colony_3
7/16 BBa_B0030(2) Colony_1	7/16 BBa_B0032(2) Colony_1
7/16 BBa_B0030(2) Colony_2	7/16 BBa_B0032(2) Colony_2
7/16 BBa_B0030(2) Colony_3	7/16 BBa_B0032(2) Colony_3
Negative Control	-
-	-

Liquid Culture

Tatsui, Matsumoto, Li, and Yamauchi

Name	medium
7/16 BBa_B0030(1) Colony_1	Plusgrow medium(CP)
7/16 BBa_B0030(1) Colony_2	Plusgrow medium(CP)
7/16 BBa_B0030(1) Colony_3	Plusgrow medium(CP)
7/16 BBa_B0030(2) Colony_1	Plusgrow medium(CP)
7/16 BBa_B0030(2) Colony_2	Plusgrow medium(CP)
7/16 BBa_B0030(2) Colony_3	Plusgrow medium(CP)
7/16 BBa_B0032(1) Colony_1	Plusgrow medium(CP)
7/16 BBa_B0032(1) Colony_2	Plusgrow medium(CP)
7/16 BBa_B0032(1) Colony_3	Plusgrow medium(CP)
7/16 BBa_B0032(2) Colony_1	Plusgrow medium(CP)
7/16 BBa_B0032(2) Colony_2	Plusgrow medium(CP)
7/16 BBa_B0032(2) Colony_3	Plusgrow medium(CP)

7/18

Miniprep

Tatsui, Matsumoto, Tsujii, Stephane, and Yamauchi

DNA	Concentration/(µg/ml)	260/280	260/230
7/16 BBa_B0030(1) Colony_1	229	1.96	1.40
7/16 BBa_B0030(1) Colony_2	209	1.95	1.50
7/16 BBa_B0030(1) Colony_3	108	2.12	2.12
7/16 BBa_B0030(2) Colony_1	-	-	-
7/16 BBa_B0030(2) Colony_2	174	2.02	1.56
7/16 BBa_B0030(2) Colony_3	158	2.01	1.68
7/16 BBa_B0032(1) Colony_1	179	2.00	2.06
7/16 BBa_B0032(1) Colony_2	-	-	-
7/16 BBa_B0032(1) Colony_3	221	1.90	1.37
7/16 BBa_B0032(2) Colony_1	225	1.89	1.37
7/16 BBa_B0032(2) Colony_2	270	1.98	1.63
7/16 BBa_B0032(2) Colony_3	194	1.89	1.33

7/30

Restriction Enzyme Digestion

No name

Sample	DNA/(µl)	EcoR1/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	Buffur/(µl)	BSA/(µl)	MilliQ/(µl)	TOTAL/(µl)
7/16 BBa_B0030(2) Colony_1	1	0.3	0	0	0	1(H)	0	7.7	10
7/16 BBa_B0030(2) Colony_1	1	0	0.3	0	0	1(M)	1	6.7	10
7/16 BBa_B0030(2) Colony_1	1	0	0	0.3	0	1(M)	0	7.7	10
7/16 BBa_B0030(2) Colony_1	1	0	0	0	0.3	1(H)	0	7.7	10
7/16 BBa_B0030(2) Colony_1(Nega)	1	0	0	0	0	1(M)	0	8	10

Electrophoresis

No name

Lane	Restriction Enzyme Digestion Products
1	7/30 BBa_B0030(2) Colony_1(E CUT)
2	7/30 BBa_B0030(2) Colony_1(X CUT)
3	7/30 BBa_B0030(2) Colony_1(S CUT)
4	7/30 BBa_B0030(2) Colony_1(P CUT)
5	7/30 BBa_B0030(2) Colony_1(Nega)
6	1kbp ladder

7/31

Transformation

Hashitani, Tatsui, Li and Yamauchi

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_E0240(RBS-GFP-DT)	2	20	22	LB(CP)
J23100(Pcon)	2	20	22	LB(AMP)

Liquid Culture

No name

Name	medium
7/31 J23100(Pcon) Colony_1	Plusgrow medium(AMP)
7/31 J23100(Pcon) Colony_2	Plusgrow medium(AMP)
7/31 J23100(Pcon) Colony_3	Plusgrow medium(AMP)
7/31 J23100(Pcon) Colony_4	Plusgrow medium(AMP)
7/31 J23100(Pcon) Colony_5	Plusgrow medium(AMP)
7/31 J23100(Pcon) Colony_6	Plusgrow medium(AMP)

Restriction Enzyme Digestion

Hashitani, Tatsui, Li and Yamauchi

7/18 RBS Sample	DNA/(µl)	EcoR1/(µl)	Spe1/(µl)	Pst1/(µl)	Xba1/(µl)	Buffur/(µl)	BSA/(µl)	MilliQ/(µl)	TOTAL/(µl)
BBa_B0032	5	0.3	0	0	0	1(H)	0	3.7	10
BBa_B0032	5	0	0.3	0	0	1(M)	0	3.7	10
BBa_B0032	5	0	0	0.3	0	1(H)	0	3.7	10
BBa_B0032	5	0	0	0	0.3	1(M)	1	2.7	10
BBa_B0032(Nega)	5	0	0	0	0	1(M)	0	4	10

8/1

Electrophoresis

Honda, Li and Yamauchi

Lane	Restriction Enzyme Digestion Products
1	1kb ladder
2	7/31 BBa_B0032(E CUT)
3	7/31 BBa_B0032(S CUT)Error
4	-
5	-
6	7/31 BBa_B0032(P CUT)
7	7/31 BBa_B0032(X CUT)
8	7/31 BBa_B0032(Nega)

PCR

Tatsui

BBa_E0240(RBS-GFP-DT)	Volume
10×buffur/(µl)	5
2mMdNTPs/(µl)	5
25mM MgSO4/(µl)	2
VF Primer/(µl)	1.5
VR Primer/(µl)	1.5
template/(µl)	0.5
KOD-plus/(µl)	1
MilliQ/(µl)	33.5
TOTAL/(µl)	50

Steps	Temparature	Time	cycle
Pre Denature	94℃	2min	1time
Denature	94℃	15sec	30cycle
Annealing	55℃	30sec	30cycle
Extension	68℃	1min	30cycle

DNA	Concentration/(µg/ml)	260/280	260/230
Product	80	1.91	1.78

8/2

Miniprep

Tatsui, Honda, Matsumoto, Yamauchi, Li, Tsujii, and Nakamura

DNA	Concentration/(µg/ml)	260/280	260/230
7/31 J23100(Pcon) Colony_1	145	2.11	3.09
7/31 J23100(Pcon) Colony_2	-	-	-
7/31 J23100(Pcon) Colony_3	160	2.01	3.13
7/31 J23100(Pcon) Colony_4	140	1.87	2.70
7/31 J23100(Pcon) Colony_5	105	2.39	5.90
7/31 J23100(Pcon) Colony_6	180	1.90	1.37

8/20

Transformation

Honda

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
7/31 BBa_E0240(RBS-GFD-DT)	2	20	22	LB(CP)
BBa_I732095	2	20	22	LB(CP)

8/21

Colony PCR

Shimazaki

NameⅠ
8/20 BBa_I732095 Colony_1
8/20 BBa_I732095 Colony_2
8/20 BBa_I732095 Colony_3
Negative control

Electrophoresis

Honda

Lane	PCR Product
1	1kb ladder
2	8/21 BBa_I732095 Colony_1
3	8/21 BBa_I732095 Colony_2
4	8/21 BBa_I732095 Colony_3
5	Negative Control

Liquid Culture

Honda and Tatsui

Name	medium
8/20 BBa_I732095 Colony_1	Plusgrow medium(CP)
8/20 BBa_I732095 Colony_2	Plusgrow medium(CP)
8/20 BBa_I732095 Colony_3	Plusgrow medium(CP)

8/22

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
8/20 BBa_I732095 Colony_1	430	1.68	2.13
8/20 BBa_I732095 Colony_2	255	1.87	1.81
8/20 BBa_I732095 Colony_3	215	1.78	1.35

Restriction Enzyme Digestion

Nakamura

Sample	DNA/(µl)	EcoR1/(µl)	Spe1/(µl)	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
8/22 BBa_I732095 Colony_1	4.7	1	1	3(H)	20.3	30
8/22 BBa_I732095 Colony_2	7.8	1	1	3(H)	17.2	30
8/22 BBa_I732095 Colony_3	9.3	1	1	3(H)	15.7	30

Transformation

Tatsui and Yamauchi

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_J04450(pSB3C5)	2	20	22	LB(CP)

8/25

Transformation

Tatsui, Kita and Li

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_J04450(pSB2K3)	2	20	22	LB(KAN)
BBa_C0051(pSB1A2)	2	20	22	LB(AMP)

Liquid Culture

Tatsui

Name	medium
8/22 BBa_J04450(pSB3C5)	Plusgrow medium(CP)*5

8/26

Miniprep

Tsujii, Honda and Matsumoto

DNA	Concentration/(µg/ml)	260/280	260/230
8/25 BBa_J04450(pSB3C5)	575	1.37	1.37

Liquid Culture

Tatsui, Matsumoto and Nakamura

Name	medium
8/25 BBa_J04450(pSB2K3)	Plusgrow medium(KAN)*5
8/25 BBa_J0051(pSB1A2)	Plusgrow medium(AMP)*2

8/27

Miniprep

No Name

DNA	Concentration/(µg/ml)	260/280	260/230
8/26 BBa_J04450(pSB2K3)	1045	1.43	1.11
8/26 BBa_J0051(pSB1A2)	790	1.39	0.90

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_J04450(pSB3T5)	2	20	22	LB(TET)

8/28

Liquid Culture

Yamauchi

Name	medium
8/27 BBa_J04450(pSB3T5)	Plusgrow medium(TET)

8/29

Miniprep

Matsumoto

DNA	Concentration/(µg/ml)	260/280	260/230
8/28 BBa_J04450(pSB3T5)	180	1.60	1.67

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
BBa_J04450(pSB4A5)	2	20	22	LB(AMP)

9/1

Colony PCR

NameⅠ
-
-
-
9/1 pSB4A5 Colony_1
9/1 pSB4A5 Colony_2
Negative Control

Restriction Enzyme Digestion

No name

Sample	DNA/(µl)	EcoR1/(µl)	Pst1/(µl)	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
8/28 Miniprep pSB3T5	25	2	2	6(H)	25	60
Negative control_1	3.7	0	0	1(H)	5.3	10
8/22 Miniprep I732095	14	3	3	9(H)	61	90
Negative control_2	1.5	0	0	1(H)	7.5	10
8/27 Miniprep pSB2K3	6	3	3	9(H)	69	90
Negative control_3	1	0	0	1(H)	8	10
8/2 Miniprep Pcon Colony_3	20	1.5	1.5	5(H)	17	45
Negative control_4	4	0	0	1(H)	5	10
8/2 Miniprep Pcon Colony_1	20	1.5	1.5	5(H)	17	45
Negative control_5	4	0	0	1(H)	5	10

Liquid Culture

No name

Name	medium
8/29 BBa_J04450(pSB4A5) Colony_1	Plusgrow medium(AMP)*2
8/1 Pcon Colony_1	Plusgrow medium(AMP)*2
8/27 pSB3T5 Colony_1	Plusgrow medium(TET)*2

9/2

Miniprep

Honda, Yamauchi and Li

DNA	Concentration/(µg/ml)	260/280	260/230
8/29 BBa_J04450(pSB4A5) Colony_1	210	1.61	1.18
8/1 Pcon Colony_1	215	1.79	1.87
8/27 pSB3T5 Colony_1	215	1.58	0.92

Gel Extraction

Matsumoto

Lane	Restriction Enzyme Digestion ProductⅠ	Volume/(µl)
1	9/1 pSB3T5 Colony_1 (Nega)	10
2	9/1 pSB3T5 Colony_1 (E+P)(Confirmation)	5
3	9/1 pSB3T5 Colony_1 (E+P)(Extraction)	55
4	1kb ladder	3
5	9/1 I732095 (Nega)	10
6	9/1 I732095 (E+P)(Confirmation)	5
7	9/1 I732095 (E+P)(Extraction)	85
8	1kb ladder	3
9	9/1 pSB2K3 (Nega)	10
10	9/1 pSB2K3 (E+P)(Confirmation)	5
11	9/1 pSB2K3 (E+P)(Extraction)	85

Lane	Sample	Volume/(µl)
1	9/1 Pcon Colony_3 (E+P)(Confirmation)	5
2	9/1 Pcon Colony_3 (E+P)(Extraction)	20
3	9/1 Pcon Colony_3 (E+P)(Extraction)	20
4	9/1 Pcon Colony_3 (Nega)	10
5	1kb ladder	3
6	9/1 Pcon Colony_1 (E+P)(Confirmation)	5
7	9/1 Pcon Colony_1 (E+P)(Extraction)	20
8	9/1 Pcon Colony_1 (E+P)(Extraction)	20
9	9/1 Pcon Colony_1 (Nega)	10

9/3

Concentration Measurement

Matsumoto, Yamauchi and Li

DNA	Concentration/(µg/ml)	260/280	260/230
pSB2K3	40	1.48	0.10
Pcon Colony_1	30	1.76	0.62
pSB3T5	50	2.35	0.50
pSB1C3	65	2.14	0.10
Pcon Colony_3	45	1.56	0.58

Ligation

No name

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
Pcon	2.1	pSB1C3	1.5	1	5	0.4	10
-(Negative Control)	0	pSB1C3	1.5	1	5	2.5	10
Pcon	1.3	pSB2K3	2.5	1	5	0.2	10
-(Negative Control)	0	pSB2K3	2.5	1	5	1.5	10
Pcon	10	pSB3T5	2.3	1	5	0.7	10
-(Negative Control)	0	pSB3T5	2.3	1	5	1.7	10

Transformation

Matsumoto

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/3 Ligation Pcon+pSB1C3	3	15	18	LB(CP)
9/3 Ligation pSB1C3(Negative Control)	8	10	18	LB(CP)
9/3 Ligation Pcon+pSB2K3	3	15	18	LB(KAN)
9/3 Ligation pSB2K3(Negative Control)	8	10	18	LB(KAN)
9/3 Ligation Pcon+pSB3T5	3	15	18	LB(TET)
9/3 Ligation pSB3T5(Negative Control)	2	10	12	LB(TET)

9/4

Colony PCR

Honda and Yamauchi

NameⅠ	NameⅡ	NameⅢ	NameⅣ
-	9/3 pSB1C3(Nega) Colony_7	9/3 Pcon+pSB3T5 Colony_5	9/3 Pcon+pSB2K3 Colony_1
-	9/3 pSB1C3(Nega) Colony_8	9/3 Pcon+pSB3T5 Colony_6	9/3 Pcon+pSB2K3 Colony_2
9/3 pSB1C3(Nega) Colony_1	9/3 Pcon+pSB3T5 Colony_1	9/3 Pcon+pSB3T5 Colony_7	9/3 Pcon+pSB2K3 Colony_3
9/3 pSB1C3(Nega) Colony_2	9/3 Pcon+pSB3T5 Colony_2	9/3 Pcon+pSB3T5 Colony_8	9/3 Pcon+pSB2K3 Colony_4
9/3 pSB1C3(Nega) Colony_3	9/3 Pcon+pSB3T5 Colony_3	9/3 Pcon+pSB3T5 Colony_9	9/3 Pcon+pSB2K3 Colony_5
9/3 pSB1C3(Nega) Colony_4	9/3 Pcon+pSB3T5 Colony_4	9/3 Pcon+pSB3T5 Colony_10	9/3 Pcon+pSB2K3 Colony_6
9/3 pSB1C3(Nega) Colony_5	9/3 pSB1C3(Nega) Colony_9	9/3 pSB3T5(Nega) Colony_1	9/3 Pcon+pSB2K3 Colony_7
9/3 pSB1C3(Nega) Colony_6	9/3 pSB1C3(Nega) Colony_10	9/3 pSB3T5(Nega) Colony_2	9/3 Pcon+pSB2K3 Colony_8

NameⅤ	NameⅥ	NameⅦ	NameⅧ
9/3 Pcon+pSB2K3 Colony_9	9/3 Pcon+pSB1C3 Colony_2	9/3 Pcon+pSB1C3 Colony_10	9/3 pSB1C3(Nega) Colony_8
9/3 Pcon+pSB2K3 Colony_10	9/3 Pcon+pSB1C3 Colony_3	9/3 pSB1C3(Nega) Colony_1	9/3 pSB1C3(Nega) Colony_9
9/3 pSB2K3(Nega) Colony_1	9/3 Pcon+pSB1C3 Colony_4	9/3 pSB1C3(Nega) Colony_2	9/3 pSB1C3(Nega) Colony_10
9/3 pSB2K3(Nega) Colony_2	9/3 Pcon+pSB1C3 Colony_5	9/3 pSB1C3(Nega) Colony_3	9/3 pSB1C3(Nega) Colony_11
9/3 pSB2K3(Nega) Colony_3	9/3 Pcon+pSB1C3 Colony_6	9/3 pSB1C3(Nega) Colony_4	-
9/3 pSB2K3(Nega) Colony_4	9/3 Pcon+pSB1C3 Colony_7	9/3 pSB1C3(Nega) Colony_5	-
9/3 pSB2K3(Nega) Colony_5	9/3 Pcon+pSB1C3 Colony_8	9/3 pSB1C3(Nega) Colony_6	-
9/3 Pcon+pSB1C3 Colony_1	9/3 Pcon+pSB1C3 Colony_9	9/3 pSB1C3(Nega) Colony_7	-

NameⅨ	NameⅩ
9/3 Pcon+pSB1C3 Colony_11	8/22 Miniprep I732095 Colony_3
Negative Control	-

Restriction Enzyme Digestion

No name

Sample	DNA/(µl)	EcoR1/(µl)	Pst1/(µl)	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
8/27 Miniprep pSB2K3	2	1	1	3(H)	23	30
8/27 Miniprep pSB2K3(Nega)	1	0	0	1(H)	8	10
9/2 Miniprep pSB3T5	10	1	1	3(H)	15	30
9/2 Miniprep pSB3T5(Nega)	3	0	0	1(H)	6	10
9/2 Miniprep pSB4A5	10	1	1	3(H)	15	30
9/2 Miniprep pSB4A5(Nega)	3	0	0	1(H)	6	10
8/22 Miniprep pSB1C3 Colony_2	2	1	1	1(H)	5	10

9/5

Electrophoresis

Honda and Matsumoto

Lane	Colony PCR ProductsⅠ	Lane	Colony PCR ProductsⅠ
1	1kb ladder	10	9/4 pSB1C3(Nega) Colony_7
2	-	11	9/4 pSB1C3(Nega) Colony_8
3	-	12	9/4 pSB1C3(Nega) Colony_9
4	9/4 pSB1C3(Nega) Colony_1	13	9/4 pSB1C3(Nega) Colony_10
5	9/4 pSB1C3(Nega) Colony_2	14	9/4 Pcon+pSB2K3 Colony_1
6	9/4 pSB1C3(Nega) Colony_3	15	9/4 Pcon+pSB2K3 Colony_2
7	9/4 pSB1C3(Nega) Colony_4	16	9/4 Pcon+pSB2K3 Colony_3
8	9/4 pSB1C3(Nega) Colony_5	17	1kb ladder
9	9/4 pSB1C3(Nega) Colony_6

Lane	Colony PCR ProductsⅡ	Lane	Colony PCR ProductsⅡ
1	1kb ladder	10	9/4 pSB3T5(Nega) Colony_2
2	9/4 Pcon+pSB2K3 Colony_4	11	9/4 Pcon+pSB2K3 Colony_1
3	9/4 Pcon+pSB2K3 Colony_5	12	9/4 Pcon+pSB2K3 Colony_2
4	9/4 Pcon+pSB2K3 Colony_6	13	9/4 Pcon+pSB2K3 Colony_3
5	9/4 Pcon+pSB2K3 Colony_7	14	9/4 Pcon+pSB2K3 Colony_4
6	9/4 Pcon+pSB2K3 Colony_8	15	9/4 Pcon+pSB2K3 Colony_5
7	9/4 Pcon+pSB2K3 Colony_9	16	9/4 Pcon+pSB2K3 Colony_6
8	9/4 Pcon+pSB3T5 Colony_10	17	1kb ladder
9	9/4 pSB3T5(Nega) Colony_1

Lane	Colony PCR ProductsⅢ	Lane	Colony PCR ProductsⅢ
1	1kb ladder	10	9/4 pSB2K3(Nega) Colony_5
2	9/4 Pcon+pSB2K3 Colony_7	11	9/4 pSB1C3(Nega) Colony_1
3	9/4 Pcon+pSB2K3 Colony_8	12	9/4 pSB1C3(Nega) Colony_2
4	9/4 Pcon+pSB2K3 Colony_9	13	9/4 pSB1C3(Nega) Colony_3
5	9/4 Pcon+pSB2K3 Colony_10	14	9/4 pSB1C3(Nega) Colony_4
6	9/4 pSB2K3(Nega) Colony_1	15	9/4 pSB1C3(Nega) Colony_5
7	9/4 pSB2K3(Nega) Colony_2	16	9/4 pSB1C3(Nega) Colony_6
8	9/4 pSB2K3(Nega) Colony_3	17	1kb ladder
9	9/4 pSB2K3(Nega) Colony_4

Lane	Colony PCR ProductsⅣ	Lane	Colony PCR ProductsⅣ
1	1kb ladder	10	9/4 Pcon+pSB1C3 Colony_5
2	9/4 pSB1C3(Nega) Colony_7	11	9/4 Pcon+pSB1C3 Colony_6
3	9/4 pSB1C3(Nega) Colony_8	12	9/4 Pcon+pSB1C3 Colony_7
4	9/4 pSB1C3(Nega) Colony_9	13	9/4 Pcon+pSB1C3 Colony_8
5	9/4 pSB1C3(Nega) Colony_10	14	9/4 Pcon+pSB1C3 Colony_9
6	9/4 Pcon+pSB1C3 Colony_1	15	9/4 Pcon+pSB1C3 Colony_10
7	9/4 Pcon+pSB1C3 Colony_2	16	8/22 Miniprep BBa_I732095 Colony_3
8	9/4 Pcon+pSB1C3 Colony_3	17	1kb ladder
9	9/4 Pcon+pSB1C3 Colony_4

Lane	Colony PCR ProductsⅤ
1	1kb ladder
2	9/4 Pcon+pSB1C3 Colony_11
3	9/4 Negative Control
4	8/22 Miniprep BBa_I732095 Colony_3
5	-
6	-
7	-
8	-

Gel Extraction

No Name

Lane	Restriction Enzyme Digestion ProductⅠ	Volume/(µl)
1	1kb ladder	5
2	9/4 pSB2K3(E+P)	5
3	-	-
4	9/4 pSB2K3(E+P)	25
5	-	-
6	9/4 pSB2K3(Nega)	10

Lane	Restriction Enzyme Digestion ProductⅡ	Volume/(µl)
1	1kb ladder	5
2	9/4 pSB3T5(E+P)	5
3	-	-
4	9/4 pSB3T5(E+P)	25
5	-	-
6	9/4 pSB3T5(Nega)	10

Lane	Restriction Enzyme Digestion ProductⅢ	Volume/(µl)
1	1kb ladder	5
2	9/4 pSB4A5(E+P)	5
3	-	-
4	9/4 pSB4A5(E+P)	25
5	-	-
6	9/4 pSB4A5(Nega)	10

Lane	Restriction Enzyme Digestion ProductⅣ	Volume/(µl)
1	1kb ladder	5
2	-	-
3	-	-
4	9/4 pSB1C3(E+P)	10
5	-	-
6	-	-

DNA	Concentration/(µg/ml)	260/280	260/230
9/4 pSB2K3(E+P)	36	1.25	0.24
9/4 pSB3T5(E+P)	10	1.00	-/td>
9/4 pSB4A5(E+P)	40	-	0.01
9/4 pSB1C3(E+P)	75	1.35	0.14

9/8

Cloning PCR

Honda and Li

Target	mamB	mamQ	mamL
2×KAPA HiFi Hotstart Ready Mix/(µl)	12.5	12.5	12.5
Fw Primer/(µl)	1.5(mamB)	1.5(mamQ)	1.5(mamL)
Rv Primer/(µl)	1.5(mamB)	1.5(mamQ)	1.5(mamL)
AMB-1 Genome/(µl)	1	1	1
MilliQ/(µl)	10	10	10
TOTAL/(µl)	25	25	25

Steps	Temparature	Time	cycle
Pre Denature	98℃	5min	1time
Denature	98℃	20sec	25cycle
Annealing	65℃	15sec	25cycle
Extension	72℃	5min	25cycle
Final elongation	72℃	5min	1time
Final hold	4℃	-	-

Ligation

Honda

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
Pcon	1	pSB3T5	10	1	11	0	22
-(Negative Control)	0	pSB1C3	3	0	3	0	6

Electrophoresis

Li

Lane	Cloning PCR Products
1	1kb ladder
2	9/8 Cloning PCR (AMB-1 mamB)
3	9/8 Cloning PCR (AMB-1 mamQ)
4	9/8 Cloning PCR (AMB-1 mamL)
5	1kb ladder

Transformation

Honda

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/8 Ligation Pcon+pSB3T5	3	30	33	LB(TET)
9/8 Ligation pSB3T5(Negative Control)	3	30	33	LB(TET)

Liquid Culture

No name

Name	medium
9/3 Transformation Pcon+pSB1C3 Colony_8	Plusgrow medium(CP)*2

9/9

DNA Purification

Li

DNA	Concentration/(µg/ml)	260/280	260/230
9/8 Cloning PCR (AMB-1 mamB)	165	1.54	1.57
9/8 Cloning PCR (AMB-1 mamQ)	250	1.69	1.92
9/8 Cloning PCR (AMB-1 mamL)	190	1.56	1.79

Miniprep

Li

DNA	Concentration/(µg/ml)	260/280	260/230
9/8 Liquid Culture Pcon+pSB1C3	90	1.65	1.17

Colony PCR

Honda and Li

NameⅠ
-
9/8 Transformation Pcon+pSB3T5 Colony_1
9/8 Transformation Pcon+pSB3T5 Colony_2
9/8 Transformation Pcon+pSB3T5 Colony_3
9/8 Transformation Pcon+pSB3T5 Colony_4
9/8 Transformation Pcon+pSB3T5 Colony_5
9/8 Transformation pSB3T5(Nega) Colony_1
Negative control

Electrophoresis

Honda and Li

Lane	Cloning PCR Products
1	1kb ladder
2	9/8 Colony PCR Pcon+pSB3T5 Colony_1
3	9/8 Colony PCR Pcon+pSB3T5 Colony_2
4	9/8 Colony PCR Pcon+pSB3T5 Colony_3
5	9/8 Colony PCR Pcon+pSB3T5 Colony_4
6	9/8 Colony PCR Pcon+pSB3T5 Colony_5
7	9/8 Colony PCR pSB3T5(Nega) Colony_1
8	9/8 Colony PCR Nega

Restriction Enzyme Digestion

No name

Sample	DNA/(µl)	Pst1/(µl)	Spe1/(µl)	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/9 Miniprep Pcon+pSB1C3	22	1	1	3(H)	3	30
9/9 Miniprep Pcon+pSB1C3(Nega)	1	0	0	1(H)	8	10
8/2 Miniprep Pcon Colony_4	14	1	1	3(H)	11	30
8/2 Miniprep Pcon Colony_4(Nega)	1	0	0	1(H)	8	10

9/10

Gel Extraction

Tatsui and Yamaura

Lane	Restriction Enzyme Digestion ProductⅠ	Volume/(µl)
1	1kb ladder	-
2	-	-
3	9/10 Digestion Pcon+pSB1C3(S+P)	-
4	-	-
5	9/10 Digestion Pcon+pSB1C3(Nega)	-
6	-	-
7	Pcon(X+P)	-
8	-	-
9	Pcon(Nega)	-
10	1kb ladder	-
11	-	-

DNA	Concentration/(µg/ml)	260/280	260/230
Pcon(X+P)	70	1.40	0.13

PCR

No Name

Target	E+X+RBS+mamB+S	X+RBS+mamL+His+S+P	X+RBS+mamQ+His+S+P
2×KAPA HiFi Hotstart Ready Mix/(µl)	12.5	12.5	12.5
Fw Primer/(µl)	0.75(E+X+RBS+mamB)	0.75(X+RBS+mamL)	0.75(X+RBS+mamQ)
Rv Primer/(µl)	0.75(S+mamB)	0.75(P+S+His+mamL)	0.75(P+S+His+mamQ)
9/9 DNA Purification Product/(µl)	Trace	Trace	Trace
MilliQ/(µl)	11	11	11
TOTAL/(µl)	25	25	25

Steps	Temparature	Time	cycle
Pre Denature	98℃	5min	1time
Denature	98℃	20sec	25cycle
Annealing	60℃	15sec	25cycle
Extension	72℃	15sec	25cycle
Final elongation	72℃	5min	1time
Final hold	12℃	-	-

Electrophoresis

Li

Lane	Cloning PCR Products
1	1kb ladder
2	9/10 PCR E+X+RBS+mamB+S(922bp)
3	9/10 PCR X+RBS+mamL+His+S+P(340bp)
4	-
5	1kb ladder
6	9/10 PCR X+RBS+mamQ+His+S+P(953bp)

DNA Purification

Honda and Yamaura

DNA	Concentration/(µg/ml)	260/280	260/230
9/10 PCR E+X+RBS+mamB+S	200	1.84	2.15
9/10 PCR X+RBS+mamL+His+S+P	120	1.69	1.84
9/10 PCR X+RBS+mamQ+His+S+P	200	1.70	2.16

Restriction Enzyme Digestion

Shimizu

Sample	DNA/(µl)	Xba1/(µl)	Pst1/(µl)	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/10 PCR E+X+RBS+mamB+S	10	1	1	3(H)	15	30
9/10 PCR X+RBS+mamL+His+S+P	16.7	1	1	3(H)	8.3	30
9/10 PCR X+RBS+mamQ+His+S+P	10	1	1	3(H)	15	30

Ligation

Tatsui and Murada

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
9/10 DNA Purification mamQ	1	YCplac111	1	1	5	2	10
9/10 DNA Purification mamL	1	YCplac111	1	1	5	2	10
9/10 DNA Purification mamB	1	YCplac111	1	1	5	2	10
Control	0	YCplac111	1	1	5	2	9

Transformation

Tatsui and Murada

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/10 Ligation mamQ+YCplac111	-	-	-	-
9/10 Ligation mamL+YCplac111	-	-	-	-
9/10 Ligation mamB+YCplac111	-	-	-	-

9/11

DNA Purification

No Name

DNA	Concentration/(µg/ml)	260/280	260/230
9/10 Digestion mamB(X+P)	65	1.68	0.51
9/10 Digestion mamL(X+P)	30	1.95	0.81
9/10 Digestion mamQ(X+P)	60	1.65	1.22

Electrophoresis

Murada

Lane	Colony PCR Products

Lane	Colony PCR Products

Lane	Colony PCR Products

Lane	Colony PCR Products

Lane	Colony PCR Products

Ligation

No Name

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
-	-	-	-	-	-	-	-

Transformation

Yamauchi

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/11 Ligation mamL	2	10	12	-
9/11 Ligation mamQ	1	5	6	-

Liquid Culture

Honda

Name	medium
9/8 Master Pcon+pSB1C3 Colony_3	Plusgrow medium(CP)
9/10 Transformation mamL+YCplac111	Plusgrow medium(AMP)
9/10 Transformation mamQ+YCplac111	Plusgrow medium(AMP)

9/12

Colony PCR

Yamaura

NameⅠ

Electrophoresis

Yamaura

Lane	Colony PCR Products

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/11 Liquid Culture Pcon+pSB1C3	110	1.83	2.63
9/11 Liquid Culture mamL+YCplac111	300	1.75	2.38
9/11 Liquid Culture mamQ+YCplac111	160	1.81	2.37

Restriction Enzyme Digestion

Yasuda

Sample	DNA/(µl)	Xba1/(µl)	Pst1/(µl)	Spe1/(µl)	Buffur/(µl)	BSA	MilliQ/(µl)	TOTAL/(µl)
9/12 Miniprep mamL+YCplac111	6.7	1	1	0	3(H)	3	15.3	30
9/12 Miniprep mamQ+YCplac111	12.5	1	1	0	3(H)	3	9.5	30
9/12 Miniprep Pcon+pSB1C3	18.1	0	1	1	3(H)	0	6.9	30

Ligation

Honda

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
9/12 Digestion mamB(E+S)	3	9/8 Digestion pSB1C3(E+S)	1	1	5	0	10
9/10 mamB	0.5	YCplac111	1	1	5	2.5	10

DNA Purification

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
mamB(E+S)	50	1.75	2.04

Transformation

Honda

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/12 Ligation mamB+pSB1C3	1	10	11	LB(CP)
9/12 Ligation mamB+YCplac111	1	10	11	LB(AMP)

Colony PCR

Li

NameⅠ	NameⅡ
9/11 Transformation mamL+pSB1A2 Colony_1	9/11 Transformation mamL+pSB1A2 Colony_9
9/11 Transformation mamL+pSB1A2 Colony_2	9/11 Transformation mamL+pSB1A2 Colony_10
9/11 Transformation mamL+pSB1A2 Colony_3	9/11 Transformation mamQ+pSB1A2 Colony_1
9/11 Transformation mamL+pSB1A2 Colony_4	9/11 Transformation mamQ+pSB1A2 Colony_2
9/11 Transformation mamL+pSB1A2 Colony_5	9/11 Transformation mamQ+pSB1A2 Colony_3
9/11 Transformation mamL+pSB1A2 Colony_6	9/11 Transformation mamQ+pSB1A2 Colony_4
9/11 Transformation mamL+pSB1A2 Colony_7	9/11 Transformation mamQ+pSB1A2 Colony_5
9/11 Transformation mamL+pSB1A2 Colony_8	9/11 Transformation mamQ+pSB1A2 Colony_6

Electrophoresis

Li

Lane	Colony PCR ProductsⅠ	Lane	Colony PCR ProductsⅠ
1	9/12 mamL+pSB1A2 Colony_1	10	9/12 mamL+pSB1A2 Colony_9
2	9/12 mamL+pSB1A2 Colony_2	11	9/12 mamL+pSB1A2 Colony_10
3	9/12 mamL+pSB1A2 Colony_3	12	9/12 mamQ+pSB1A2 Colony_1
4	9/12 mamL+pSB1A2 Colony_4	13	9/12 mamQ+pSB1A2 Colony_2
5	9/12 mamL+pSB1A2 Colony_5	14	9/12 mamQ+pSB1A2 Colony_3
6	9/12 mamL+pSB1A2 Colony_6	15	9/12 mamQ+pSB1A2 Colony_4
7	9/12 mamL+pSB1A2 Colony_7	16	9/12 mamQ+pSB1A2 Colony_5
8	9/12 mamL+pSB1A2 Colony_8	17	9/12 mamQ+pSB1A2 Colony_6
9	1kb ladder

Colony PCR

Honda

NameⅠ
9/11 Transformation mamL+pSB1A2 Green_1
9/11 Transformation mamL+pSB1A2 Green_2
9/11 Transformation mamL+pSB1A2 Green_3
9/11 Transformation mamL+pSB1A2 Green_4
9/11 Transformation mamL+pSB1A2 Green_5
9/11 Transformation mamL+pSB1A2 Black_7
9/11 Transformation mamL+pSB1A2 Black_8
9/11 Transformation mamQ+pSB1A2 Black_1

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ
1	9/12 mamL+pSB1A2 Green_1
2	9/12 mamL+pSB1A2 Green_2
3	9/12 mamL+pSB1A2 Green_3
4	9/12 mamL+pSB1A2 Green_4
5	9/12 mamL+pSB1A2 Green_5
6	9/12 mamL+pSB1A2 Black_7
7	9/12 mamL+pSB1A2 Black_8
8	9/12 mamQ+pSB1A2 Black_1
9	1kb ladder

Liquid Culture

Yamauchi

Name	medium
9/11 Transformation mamQ+pSB1A2 Colony_1	Plusgrow medium(AMP)
9/11 Transformation mamQ+pSB1A2 Colony_2	Plusgrow medium(AMP)
9/11 Transformation mamQ+pSB1A2 Colony_3	Plusgrow medium(AMP)
9/11 Transformation mamQ+pSB1A2 Colony_4	Plusgrow medium(AMP)
9/11 Transformation mamQ+pSB1A2 Colony_5	Plusgrow medium(AMP)
9/11 Transformation mamQ+pSB1A2 Colony_6	Plusgrow medium(AMP)

9/13

Miniprep

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
9/12 Liquid Culture mamQ+pSB1A2 Colony_1 Error	-	-	-
9/12 Liquid Culture mamQ+pSB1A2 Colony_2 Error	-	-	-
9/12 Liquid Culture mamQ+pSB1A2 Colony_3 Error	-	-	-
9/12 Liquid Culture mamQ+pSB1A2 Colony_4	80	2.02	2.76
9/12 Liquid Culture mamQ+pSB1A2 Colony_5	70	2.13	3.41
9/12 Liquid Culture mamQ+pSB1A2 Colony_6	110	1.96	1.70
9/12 Liquid Culture Pcon+pSB1C3	110	1.96	1.70

PCR Labeling and Sequence

No Name

Target	9/13 mamQ+pSB1A2 Colony_4	9/13 mamQ+pSB1A2 Colony_5	9/13 mamQ+pSB1A2 Colony_6	Pcon+pSB1A2	9/13 mamQ+pSB1A2 Colony_4	9/13 mamQ+pSB1A2 Colony_5	9/13 mamQ+pSB1A2 Colony_6
Template/(µl)	5	4	6	4	5	6	4
Big dye/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75	1.75	1.75	1.75
Primer/(µl)	0.5(VF)	0.5(VF)	0.5(VF)	0.5(VF)	0.5(VR)	0.5(VR)	0.5(VR)
MilliQ/(µl)	2.75	1.75	3.75	3.75	2.75	1.75	3.75
TOTAL/(µl)	10.5	10.5	10.5	10.5	10.5	10.5	10.5

Target	9/12 mamQ+YCplac111	9/12 mamL+YCplac111	9/12 mamQ+YCplac111	9/12 mamL+YCplac111	9/12 mamQ+YCplac111
Template/(µl)	3	1.5	3	1.5	3
Big dye/(µl)	0.5	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75	1.75
Primer/(µl)	0.5(M13F)	0.5(M13F)	0.5(M13R)	0.5(M13R)	0.5(seqpLQB-2)
MilliQ/(µl)	4.75	6.25	4.75	6.25	4.75
TOTAL/(µl)	10.5	10.5	10.5	10.5	10.5

Gel Extraction

No Name

Lane	Restriction Enzyme Digestion ProductⅠ	Volume/(µl)
1	1kb ladder	-
2	-	-
3	9/12 Digestion mamQ+YCpla111(X+P)(992bp)	-
4	-	-
5	-	-
6	-	-
7	9/12 Digestion mamL+YCpla111(X+P)(340bp)	-
8	-	-
9	9/12 Digestion Pcon+pSB1C3(Nega)(5600bp)	-
10	-	-
11	9/12 Digestion Pcon+pSB1C3(S+P)(2070bp)	-

DNA	Concentration/(µg/ml)	260/280	260/230
9/12 Digestion mamL+YCpla111(X+P)	10	1.00	0.70
9/12 Digestion Pcon+pSB1C3(S+P)	150	1.25	0.71

Restriction Enzyme Digestion

Li

Sample	DNA/(µl)	Xba1/(µl)	Pst1/(µl)	Buffur/(µl)	BSA	MilliQ/(µl)	TOTAL/(µl)
9/13 Miniprep mamQ+pSB1A2 Colony_4	12.5	0.5	0.5	1.7(M)	1.6	0	16.8
9/13 Miniprep mamQ+pSB1A2 Colony_5	14.3	0.5	0.5	1.9(M)	1.86	0	19.06
9/13 Miniprep mamQ+pSB1A2 Colony_6	9.1	0.5	0.5	1.5(M)	1.5	1.9	15
9/13 Miniprep mamQ+pSB1A2 Colony_6(Nega)	3	0	0	0.5(M)	0.5	1	5

Ligation

Yasuda

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
9/13 Gel Extraction mamL(X+P)	3	Pcon+pSB1C3(S+P)	1	1	5	0	10

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/12 Liquid Culture Pcon+pSB1C3	240	1.78	1.59

9/14

Gel Extraction

Honda

Lane	Restriction Enzyme Digestion ProductⅠ	Volume/(µl)
1	1kb ladder	3
2	-	-
3	9/13 mamQ Colony_4(X+P)	16.8
4	-	-
5	1kb ladder	3
6	-	-
7	9/13 mamQ Colony_5(X+P)	19.06
8	-	-
9	9/13 mamQ Colony_6(Nega)	5
10	-	-
11	9/13 mamQ Colony_6(X+P)	15

Ligation

Tatsui

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
mamB(E+S)	4	pSB1C3(E+S)	3	1	8	0	16
mamL(X+P)	3.3	pSB1C3(E+S)	0.7	1	5	0	10

PCR

Tatsui

Target	E+X+RBS+mamB+S
2×KAPA HiFi Hotstart Ready Mix/(µl)	12.5
Fw Primer/(µl)	0.75(E+X+RBS+mamB)
Rv Primer/(µl)	0.75(S+mamB)
9/9 DNA Purification Product/(µl)	Trace
MilliQ/(µl)	11
TOTAL/(µl)	25

Steps	Temparature	Time	cycle
Pre Denature	98℃	5min	1time
Denature	98℃	20sec	25cycle
Annealing	60℃	15sec	25cycle
Extension	72℃	15sec	25cycle
Final elongation	72℃	5min	1time
Final hold	12℃	-	-

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/14 Ligation Pcon+mamL+pSB1C3	1	10	11	LB(CP)
9/14 Ligation Pcon+mamL+pSB1C3(Nega)	1	10	11	LB(CP)
9/14 Ligation mamB+pSB1C3	1	10	11	LB(CP)

9/15

Colony PCR

Tatsui

NameⅠ	NameⅡ
9/14 Transformation mamB+pSB1C3 Colony_1	9/14 Transformation mamB+pSB1C3 Colony_9
9/14 Transformation mamB+pSB1C3 Colony_2	9/14 Transformation mamB+pSB1C3 Colony_10
9/14 Transformation mamB+pSB1C3 Colony_3	9/14 Transformation mamB+pSB1C3 Colony_11
9/14 Transformation mamB+pSB1C3 Colony_4	9/14 Transformation mamB+pSB1C3 Colony_12
9/14 Transformation mamB+pSB1C3 Colony_5	9/14 Transformation mamB+pSB1C3 Colony_13
9/14 Transformation mamB+pSB1C3 Colony_6	9/14 Transformation mamB+pSB1C3 Colony_14
9/14 Transformation mamB+pSB1C3 Colony_7	9/14 Transformation mamB+pSB1C3 Colony_15
9/14 Transformation mamB+pSB1C3 Colony_8	-

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ
1	9/14 mamB+pSB1C3 Colony_1
2	9/14 mamB+pSB1C3 Colony_2
3	9/14 mamB+pSB1C3 Colony_3
4	9/14 mamB+pSB1C3 Colony_4
5	9/14 mamB+pSB1C3 Colony_5
6	9/14 mamB+pSB1C3 Colony_6
7	9/14 mamB+pSB1C3 Colony_7
8	9/14 mamB+pSB1C3 Colony_8
9	1kb ladder
10	9/14 mamB+pSB1C3 Colony_9
11	9/14 mamB+pSB1C3 Colony_10
12	9/14 mamB+pSB1C3 Colony_11
13	9/14 mamB+pSB1C3 Colony_12
14	9/14 mamB+pSB1C3 Colony_13
15	9/14 mamB+pSB1C3 Colony_14
16	9/14 mamB+pSB1C3 Colony_15

Colony PCR

No Name

NameⅠ
9/14 Transformation Pcon+mamL+SBpSB1C3 Colony_1
9/14 Transformation mamB+pSB1C3 Colony_9

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
mamB+YCplac111	1	10	11	LB(AMP)
Pcon+mamL+pSB1C3	1	10	11	LB(CP)

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
mamB+pSB1C3 Colony_9	-	-	-
mamB+pSB1C3 Colony_10	-	-	-
mamB+pSB1C3 Colony_11	-	-	-
mamL+pSB1A2 Colony_1	170	1.74	1.41
mamL+pSB1A2 Colony_2	140	1.95	1.43
mamL+pSB1A2 Colony_3	135	1.95	1.60
mamL+pSB1A2 Colony_4	-	-	-
mamL+pSB1A2 Colony_5	-	-	-
mamL+pSB1A2 Colony_6	-	-	-

Liquid Culture

Honda

Name	medium
9/14 Transformation Pcon+mamL+pSB1C3 Colony_1	Plusgrow medium(CP)
9/14 Transformation mamB+pSB1C3 Colony_9	Plusgrow medium(CP)
9/14 Transformation mamB+pSB1C3 Colony_10	Plusgrow medium(CP)
9/14 Transformation mamB+pSB1C3 Colony_11	Plusgrow medium(CP)

Restriction Enzyme Digestion

Li

Sample	DNA/(µl)	EcoR1/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	MilliQ/(µl)	Buffur/(µl)	TOTAL/(µl)
9/15 DNA Purification mamB	25	1	0	1	0	0	0	3(H)	30
9/15 Mniprep mamL+pSB1A2 Colony_1	11.8	0	1	0	1	3	10.2	3(M)	30
9/15 Mniprep mamL+pSB1A2 Colony_1(Nega)	0.6	0	0	0	0	1	8.4	1(M)	10
9/15 Mniprep mamL+pSB1A2 Colony_2	14.3	0	1	0	1	3	7.7	3(M)	30
9/15 Mniprep mamL+pSB1A2 Colony_2(Nega)	0.7	0	0	0	0	1	8.3	1(M)	10
9/15 Mniprep mamL+pSB1A2 Colony_3	14.8	0	1	0	1	3	7.2	3(M)	30
9/15 Mniprep mamL+pSB1A2 Colony_3(Nega)	0.7	0	0	0	0	1	8.3	1(M)	10
9/15 Mniprep mamL+pSB1A2 Colony_4	13.3	0	1	0	1	3	8.7	3(M)	30
9/15 Mniprep mamL+pSB1A2 Colony_4(Nega)	0.7	0	0	0	0	1	8.3	1(M)	10
9/13 Pcon+pSB1C3	20	0	0	1	1	0	5	3(H)	30
9/13 Pcon+pSB1C3(Nega)	1	0	0	0	0	0	6	3(H)	10

PCR

Honda

Target	mamB Colony_10	mamB Colony_11
2×PrimeSTAR Max Premix/(µl)	25	25
Fw mamB Mutation Primer/(µl)	1	1
Rv mamB Mutation Primer/(µl)	1	1
9/15 Miniprep mamB+pSB1C3/(µl)	Colony_10(Trace)	Colony_11(Trace)
MilliQ/(µl)	23	23
TOTAL/(µl)	50	50

Steps	Temparature	Time	cycle
Pre Denature	98℃	2min	1time
Denature	98℃	10sec	30cycle
Annealing	55℃	15sec	30cycle
Extension	72℃	15sec	30cycle
Final elongation	72℃	5min	1time
Final hold	12℃	-	-

9/16

PCR Labeling and Sequence

No Name

Target	9/15 Pcon+mamL+pSB1C3	9/15 mamL+pSB1A2 Colony_1	9/15 mamL+pSB1A2 Colony_2	9/15 mamL+pSB1A2 Colony_3	9/15 mamL+pSB1A2 Colony_4	9/15 mamB+pSB1C3 Colony_9	9/15 mamB+pSB1C3 Colony_10	9/15 mamB+pSB1C3 Colony_11
Template/(µl)	1.8	2.35	2.9	3.0	3.0	1.14	1.2	1.2
Big dye/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75
Primer(VF)/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5
MilliQ/(µl)	5.95	5.4	4.85	4.75	4.75	6.61	6.55	6.55
TOTAL/(µl)	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5

Target	9/15 Pcon+mamL+pSB1C3	9/15 mamL+pSB1A2 Colony_1	9/15 mamL+pSB1A2 Colony_2	9/15 mamL+pSB1A2 Colony_3	9/15 mamB+pSB1C3 Colony_9	9/15 mamB+pSB1C3 Colony_10	9/15 mamB+pSB1C3 Colony_11
Template/(µl)	1.8	2.35	2.9	3.0	1.14	1.2	1.2
Big dye/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75	1.75	1.75	1.75
Primer(VR)/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5
MilliQ/(µl)	5.95	5.4	4.85	4.75	6.61	6.55	6.55
TOTAL/(µl)	10.5	10.5	10.5	10.5	10.5	10.5	10.5

Steps	Temparature	Time	cycle
Pre Denature	96℃	2min	1time
Denature	96℃	10sec	30cycle
Annealing	55℃	5sec	30cycle
Extension	72℃	4min	30cycle
Final elongation	72℃	1min	1time
Final hold	4℃	-	-

Gel Extraction

Honda

Lane	Restriction Enzyme Digestion ProductⅠ	Volume/(µl)
1	1kb ladder	-
2	1kb ladder	-
3	9/15 mamL Colony_1(X+P)	-
4	-	-
5	9/15 mamL Colony_2(Nega)	-
6	-	-
7	9/15 mamL Colony_2(X+P)	-
8	1kb ladder	-
9	1kb ladder	-
10	9/15 mamL Colony_3(Nega)	-
11	9/15 mamL Colony_3(X+P)	-

Lane	Restriction Enzyme Digestion ProductⅡ	Volume/(µl)
1	1kb ladder	-
2	-	-
3	-	-
4	9/15 mamQ(X+P)	-
5	-	-
6	9/15 mamQ(Nega)	-

DNA	Concentration/(µg/ml)	260/280	260/230
mamL Colony_1	45	1.69	0.60
mamL Colony_2	60	1.33	0.70
mamL Colony_3	40	1.76	0.08
mamQ	65	1.35	0.83

Dephosphorylation

Honda

Sample/(µL)
9/15 Digestion Pcon+pSB1C3(S+P)	-
9/15 Gel Extraction Pcon+pSB1C3(S+P)	-

DNA Purification

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/15 Mutation PCR mamB+pSB1C3 Colony_10	225	1.64	1.74
9/15 Mutation PCR mamB+pSB1C3 Colony_11	205	1.59	1.76

Gel Extraction

Yamauchi

Lane	SampleⅠ	Volume/(µl)
1	1kb ladder	-
2	-	-
3	9/15 Digestion Pcon+pSB1C3(S+P)	-
4	-	-
5	1kb ladder	-
6	-	-
7	9/15 Gel Extraction Pcon+pSB1C3(S+P)	-
8	-	-
9	1kb ladder	-
10	-	-
11	-	-

Transformation

Honda and Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/16 DNA Purification mamB+pSB1C3 Colony_10	1	10	11	LB(CP)
9/16 DNA Purification mamB+pSB1C3 Colony_11	1	10	11	LB(CP)

Restriction Enzyme Digestion

No Name

Sample	DNA/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	MilliQ/(µl)	Buffur/(µl)	TOTAL/(µl)
9/15 mamQ+pSB1A2 Colony_4	26.7	2	0	2	6	17.3	6(M)	60
9/15 mamQ+pSB1A2 Colony_4(Nega)	0.7	0	0	0	1	7.3	1(M)	10
9/15 Pcon+mamL+pSB1C3	15	0	2	2	0	35	6(H)	60
9/15 Pcon+mamL+pSB1C3(Nega)	0.5	0	0	0	0	8.5	1(H)	10

PCR

Tatsui

Target	E+Pcon+X+RBS+mamB+His+S(*2)
2×KAPA HiFi Hotstart Ready Mix/(µl)	12.5
Fw E+Pcon+X+RBS+mamB/(µl)	0.75
Rv S+His+mamB/(µl)	0.75
9/9 DNA Purification mamB/(µl)	Trace
MilliQ/(µl)	11
TOTAL/(µl)	25

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/15 mamB+pSB1C3 Colony_9	350	1.68	1.81
9/15 mamB+pSB1C3 Colony_10	325	1.65	1.50
9/15 mamB+pSB1C3 Colony_11	340	1.67	1.68
Pcon+mamL+pSB1C3	220	1.75	2.09

9/17

Colony PCR

Tatsui

NameⅠ
9/16 Transformation Mutation mamB Colony_11_1
9/16 Transformation Mutation mamB Colony_11_2
9/16 Transformation Mutation mamB Colony_11_3
9/16 Transformation Mutation mamB Colony_11_4
9/16 Transformation Mutation mamB Colony_10_1
9/16 Transformation Mutation mamB Colony_10_2
9/16 Transformation Mutation mamB Colony_10_3
9/16 Transformation Mutation mamB Colony_10_4

Miniprep

Tatsui and Yamauchi

DNA	Concentration/(µg/ml)	260/280	260/230
9/15 Pcon+pSB1C3 Colony_3	110	1.66	1.48

Gel Extraction

Yamauchi

Lane	SampleⅠ	Volume/(µl)
1	9/16 Mutation PCR Pcon+mamB+His	-
2	Pcon+mamL(Nega)	-
3	Pcon+mamL(S+P)	-
4	1kb ladder	-
5	9/16 Mutation PCR Pcon+mamB+His	-
6	-	-
7	mamQ+pSB1A2 Colony_4(X+P)	-
8	1kb ladder	-
9	mamQ(Nega)	-
10	-	-
11	mamQ+pSB1A2 Colony_4(X+P)	-

DNA	Concentration/(µg/ml)	260/280	260/230
Pcon+mamB+His	245	1.87	2.10
mamQ+pSB1A2 Colony_4(X+P)	35	1.87	0.580
Pcon+mamL(S+P)	285 Error	1.14	0.85

Ligation

Tatsui

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
mamQ(X+P)	3	Pcon+mamL(S+P)	1	1	5	0	10

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/17 Ligation Pcon+mamL+mamQ+pSB1C3	1	10	11	LB(CP)

Restriction Enzyme Digestion

Tatsui

Sample	DNA/(µl)	EcoR1/(µl)	Spe1/(µl)	Pst1/(µl)	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/17 Gel Extraction Pcon+mamB+His	16.3	2	2	0	6(H)	33.7	60
9/17 Gel Extraction Pcon+mamB+His(Nega)	1	0	0	0	1(H)	8	10
9/17 Miniprep Pcon+pSB1C3	36.4	0	2	2	6(H)	13.6	60
9/17 Miniprep Pcon+pSB1C3(Nega)	1	0	0	0	1(H)	8	10

Liquid Culture

Tatsui

Name	medium
Mutation mamB Colony_10_3	Plusgrow medium(CP)
Mutation mamB Colony_10_4	Plusgrow medium(CP)
Mutation mamB Colony_11_3	Plusgrow medium(CP)
Mutation mamB Colony_11_4	Plusgrow medium(CP)
mamQ+pSB1A2 Colony_4	Plusgrow medium(AMP)*2
Pcon+mamL Colony_1	Plusgrow medium(CP)*3.5

9/18

Miniprep

Tatsui and Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/17 Liquid Culture Mutation mamB Colony_10_3	355	1.69	2.02
9/17 Liquid Culture Mutation mamB Colony_10_4	265	1.52	1.55
9/17 Liquid Culture Mutation mamB Colony_11_3	355	1.62	1.77
9/17 Liquid Culture Mutation mamB Colony_11_4	250	1.62	1.51
9/17 Liquid Culture mamQ+pSB1A2 Colony_4	290	1.41	1.10
9/17 Liquid Culture Pcon+mamL+pSB1C3 Colony_1	85	1.47	1.56

PCR Labeling and Sequence

No Name

Target	9/18 Miniprep Mutation mamB Colony_10_3	9/18 Miniprep Mutation mamB Colony_10_4	9/18 Miniprep Mutation mamB Colony_11_3	9/18 Miniprep Mutation mamB Colony_11_4	9/18 Miniprep Mutation mamB Colony_10_3	9/18 Miniprep Mutation mamB Colony_10_4	9/18 Miniprep Mutation mamB Colony_11_3	9/18 Miniprep Mutation mamB Colony_11_4
Template/(µl)	1.1	1.5	1.1	1.6	1.1	1.5	1.1	1.6
Big dye/(µl)	2	2	2	2	2	2	2	2
5×Buffer/(µl)	1	1	1	1	1	1	1	1
Primer/(µl)	0.16(VF)	0.16(VF)	0.16(VF)	0.16(VF)	0.16(VR)	0.16(VR)	0.16(VR)	0.16(VR)
MilliQ/(µl)	5.74	5.34	5.74	5.24	5.74	5.34	5.74	5.24
TOTAL/(µl)	10	10	10	10	10	10	10	10

Target	9/18 Miniprep Mutation mamB Colony_10_3	9/18 Miniprep Mutation mamB Colony_10_4	9/18 Miniprep Mutation mamB Colony_11_3	9/18 Miniprep Mutation mamB Colony_11_4
Template/(µl)	1.1	1.5	1.1	1.6
Big dye/(µl)	2	2	2	2
5×Buffer/(µl)	1	1	1	1
Primer/(µl)	0.16(pQLB seq_2)	0.16(pQLB seq_2)	0.16(pQLB seq_2)	0.16(pQLB seq_2)
MilliQ/(µl)	5.74	5.34	5.74	5.24
TOTAL/(µl)	10	10	10	10

Steps	Temparature	Time	cycle
Pre Denature	96℃	2min	1time
Denature	96℃	10sec	30cycle
Annealing	50℃	5sec	30cycle
Extension	60℃	4min	30cycle
Final elongation	4℃	1min	1time
Final hold	4℃	-	-

Colony PCR

Tatsui

NameⅠ	NameⅡ
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_1	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_9
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_2	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_10
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_3	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_11
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_4	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_12
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_5	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_13
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_6	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_14
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_7	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_15
9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_8	9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_16

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ
1	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_1
2	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_2
3	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_3
4	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_4
5	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_5
6	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_6
7	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_7
8	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_8
9	1kb ladder
10	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_9
11	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_10
12	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_11
13	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_12
14	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_13
15	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_14
16	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_15
17	9/18 Pcon+mamL+mamQ+pSB1C3 Colony_16

DNA Purification

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
9/17 Digestion Pcon+mamB+His(E+S)	165	-	-

Gel Extraction

Tatsui

Lane	SampleⅠ	Volume/(µl)
1	-	-
2	1kb ladder	-
3	9/17 Digestion Pcon+pSB1C3(Nega)	-
4	9/17 Digestion Pcon+pSB1C3(S+P)	-
5	-	-
6	-	-

Lane	SampleⅡ	Volume/(µl)
1	-	-
2	-	-
3	1kb ladder	-
4	9/17 Digestion Pcon+pSB1C3(S+P)	-
5	-	-
6	-	-

DNA	Concentration/(µg/ml)	260/280	260/230
9/17 Digestion Pcon+pSB1C3	-	-	-

Ligation

Tatsui

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	10*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
mamQ(X+P)	6	9/18 Gel Extraction Pcon+pSB1C3(S+P)	Trace	0.5	1	2.5	10
9/18 DNA Purification Pcon+mamB+His(E+S)	5	9/14 pSB3T5(E+S)	2	0.5	1	1.5	10

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/18 Ligation Pcon+mamQ+pSB1C3	1	10	11	LB(CP)
9/18 Ligation Pcon+mamB+His+pSB3T5	1	10	11	LB(TET)

Liquid Culture

Tatsui

Name	medium
pSB3T5	Plusgrow medium(TET)*2
9/17 Transformation Pcon+mamL+mamQ+pSB1C3	Plusgrow medium(CP)

Restriction Enzyme Digestion

No Name

Sample	DNA/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/18 Miniprep Mutation mamB Colony_10_3	11.2	2	0	2	0.8	8(D)	56	80
9/18 Miniprep Mutation mamB Colony_10_3(Nega)	1	0	0	0	0	1(D)	8	10
9/18 Miniprep Mutation mamB Colony_10_4	15.1	2	0	2	0.8	8(D)	52.1	80
9/18 Miniprep Mutation mamB Colony_10_4(Nega)	1	0	0	0	0	1(D)	8	10
9/18 Miniprep Mutation mamB Colony_11_3	11.2	2	0	2	0.8	8(D)	56	80
9/18 Miniprep Mutation mamB Colony_11_3(Nega)	1	0	0	0	0	1(D)	8	10
9/18 Miniprep Mutation mamB Colony_11_4	16	2	0	2	0.8	8(D)	51.2	80
9/18 Miniprep Mutation mamB Colony_11_4(Nega)	1	0	0	0	0	1(D)	8	10
9/18 Miniprep mamQ+pSB1A2	34.5	5	0	5	2	20(D)	133.5	200
9/18 Miniprep mamQ+pSB1A2(Nega)	1	0	0	0	0	1(D)	8	10
9/17 Miniprep Pcon+pSB1C3	40	0	2	2	0.8	8(B)	27.2	80
9/17 Miniprep Pcon+pSB1C3(Nega)	1	0	0	0	0	1(B)	8	10
9/18 Miniprep Pcon+mamL+pSB1C3	47	0	2	2	0.8	8(B)	20.2	80
9/18 Miniprep Pcon+mamL+pSB1C3(Nega)	1	0	0	0	0	1(B)	8	10

9/19

Miniprep

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
9/18 Liquid Culture pSB3T5	115	1.52	1.22
9/18 Liquid Culture Pcon+mamL+mamQ+pSB1C3	75	1.59	1.20

PCR Labeling and Sequence

No Name

Target	9/19 Miniprep Pcon+mamL+mamQ+pSB1C3	9/19 Miniprep Pcon+mamL+mamQ+pSB1C3	9/19 Miniprep Pcon+mamL+mamQ+pSB1C3	9/19 Miniprep Pcon+mamL+mamQ+pSB1C3
Template/(µl)	3.5	3.5	3.5	3.5
Big dye/(µl)	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75
Primer/(µl)	0.5(VF)	0.5(VR)	0.5(seq_1)	0.5(seq_2)
MilliQ/(µl)	4.25	4.25	4.25	4.25
TOTAL/(µl)	10.5	10.5	10.5	10.5

Steps	Temparature	Time	cycle
Pre Denature	96℃	2min	1time
Denature	96℃	10sec	30cycle
Annealing	50℃	5sec	30cycle
Extension	60℃	4min	30cycle
Final elongation	4℃	1min	1time
Final hold	4℃	-	-

Gel Extraction

Tatsui

Lane	SampleⅠ	Volume/(µl)
1	-	-
2	-	-
3	9/18 Digestion Mutation mamB Colony_10_3(X+P)	40
4	9/18 Digestion Mutation mamB Colony_10_3(Nega)	10
5	1kb ladder	-
6	-	-
7	9/18 Digestion Mutation mamB Colony_10_3(X+P)	40
8	-	-
9	1kb ladder	-
10	9/18 Digestion Mutation mamB Colony_10_4(Nega)	10
11	9/18 Digestion Mutation mamB Colony_10_4(X+P)	40

Lane	SampleⅡ	Volume/(µl)
1	9/18 Digestion mamQ+pSB1A2(X+P)	200
2	-	-
3	-	-
4	-	-
5	-	-
6	-	-

Lane	SampleⅢ	Volume/(µl)
1	100b ladder	-
2	9/18 Digestion Pcon+pSB1C3(Nega)	10
3	9/18 Digestion Pcon+pSB1C3(S+P)	80

DNA	Concentration/(µg/ml)	260/280	260/230
mamB Colony_10_3(X+P)	-	-	-
mamB Colony_10_4(X+P)	-	-	-
mamQ+pSB1A2(X+P)	-	-	-
Pcon+pSB1C3(S+P)	-	-	-

Colony PCR

Tatsui

NameⅠ
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_1
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_2
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_3
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_4
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_5

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ
1	-
2	-
3	Pcon+mamQ+pSB1C3 Colony_1
4	Pcon+mamQ+pSB1C3 Colony_2
5	Pcon+mamQ+pSB1C3 Colony_3
6	Pcon+mamQ+pSB1C3 Colony_4
7	Pcon+mamQ+pSB1C3 Colony_5
8	-

Restriction Enzyme Digestion

Tatsui

Sample	DNA/(µl)	EcoR1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/19 Miniprep Pcon+mamL+mamQ+pSB1C3	34.7	0	2	2	0.8	8(B)	32.5	80
9/19 Miniprep pSB3T5	53.3	2	2	0	0.8	8(B)	14	80
9/19 Miniprep pSB3T5(Nega)	1	0	0	0	0	1(B)	8	10

PCR

Tatsui

Target	Pcon+mamB+His
KOD Plus/(µl)	1
10×Buffer/(µl)	5
2mM dNTPS/(µl)	5
25mM MgSO4/(µl)	3
Fw Primer(E+Pcon+X+RBS+mamB)/(µl)	2
Rv Primer(S+His+mamB)/(µl)	2
Template/(µl)	0.5
MilliQ/(µl)	31.5
Total/(µl)	50

Steps	Temparature	Time	cycle
Pre Denature	98℃	2min	1time
Denature	98℃	10sec	25cycle
Annealing	55℃	15sec	25cycle
Extension	72℃	1min	25cycle
Final elongation	72℃	5min	1time
Final hold	12℃	-	-

DNA Purification

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/18 Digestion mamL+pSB1C3(S+P)	55	1.66	1.66
9/19 PCR Pcon+mamB+His	150	1.63	1.52

Restriction Enzyme Digestion

Honda

Sample	DNA/(µl)	EcoR1/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/19 DNA Purification Pcon+mamB+His	20	1	0	1	0	0.8	8(B)	49.2	80

Liquid Culture

Tatsui

Name	medium
9/18 Transformation Pcon+mamB+His+pSB3T5 Colony_1	Plusgrow medium(TET)
9/18 Transformation Pcon+mamB+His+pSB3T5 Colony_2	Plusgrow medium(TET)
9/18 Transformation Pcon+mamB+His+pSB3T5 Colony_3	Plusgrow medium(TET)
9/18 Transformation Pcon+mamB+His+pSB3T5 Colony_4	Plusgrow medium(TET)
9/18 Transformation Pcon+mamB+His+pSB3T5 Colony_5	Plusgrow medium(TET)

Colony PCR

Tatsui

NameⅠ
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_1
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_2
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_3
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_4
9/18 Transformation Pcon+mamQ+pSB1C3 Colony_5

9/20

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ
1	-
2	100b ladder
3	Pcon+mamQ+pSB1C3 Colony_1
4	Pcon+mamQ+pSB1C3 Colony_2
5	Pcon+mamQ+pSB1C3 Colony_3
6	Pcon+mamQ+pSB1C3 Colony_4
7	Pcon+mamQ+pSB1C3 Colony_5

Miniprep

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
9/19 Liquid Culture Pcon+mamQ+pSB1C3 Colony_3	-	-	-
9/19 Liquid Culture Pcon+mamQ+pSB1C3 Colony_5	-	-	-

Colony PCR

Tatsui

NameⅠ
Pcon+mamB+His+pSB3T5 Colony_1(VF+VR)
Pcon+mamB+His+pSB3T5 Colony_1(seq_4+VR)

Electrophoresis

Yasuda

Lane	Colony PCR ProductsⅠ
1	-
2	100b ladder
3	100b ladder
4	Pcon+mamB+His+pSB3T5 Colony_1(VF+VR)
5	Pcon+mamB+His+pSB3T5 Colony_1(seq_4+VR)
6	100b ladder

Restriction Enzyme Digestion

Honda

Sample	DNA/(µl)	EcoR1/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	Buffur/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/18 Miniprep Mutation mamB Colony_10_3	11.2	0	2	0	2	0.8	8(D)	56	80
9/18 Miniprep Mutation mamB Colony_10_3(Nega)	1	0	0	0	0	0	1(D)	8	10
9/18 Miniprep Mutation mamB Colony_10_4	15.1	0	2	0	2	0.8	8(D)	56	83.9
9/18 Miniprep Mutation mamB Colony_10_4(Nega)	1	1	0	1	0	0	1(D)	8	10

Gel Extraction

Tatsui

Lane	SampleⅠ	Volume/(µl)
1	-	-
2	100b ladder	-
3	Digestion Mutation mamB Colony_10_3(X+P)	-
4	-	-
5	-	-
6	-	-
7	Digestion Mutation mamB Colony_11_3(X+P)	-
8	Digestion Mutation mamB Colony_11_3(Nega)	-
9	1kb ladder	-
10	-	-
11	Digestion Mutation mamB Colony_11_3(X+P)	-

Lane	SampleⅡ	Volume/(µl)
1	-	-
2	100b ladder	-
3	9/19 Digestion pSB3T5(Nega)	-
4	9/19 Digestion pSB3T5(E+S)	-

Lane	SampleⅢ	Volume/(µl)
1	-	-
2	100b ladder	-
3	Digestion Mutation mamB Colony_11_4(X+P)	-
4	Digestion Mutation mamB Colony_11_4(Nega)	-

DNA	Concentration/(µg/ml)	260/280	260/230
mamB Colony_10_3(X+P)	60	-	-
mamB Colony_11_3(X+P)	85	1.38	2.04
mamB Colony_11_4(X+P)	60	0.58	2.32
pSB3T5(E+S)	70	0.44	2.04

DNA Purification

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
Pcon+mamL+mamQ(S+P)	-	-	-

Ligation

Tatsui

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	2*Buffer/(µl)	Total/(µl)
mamB Colony_10_3(X+P)	1.7	Pcon+mamL+mamQ(S+P)	2.3	1	5	10
mamB Colony_10_4(X+P)	1.7	Pcon+mamL+mamQ(S+P)	2.3	1	5	10
mamB Colony_11_3(X+P)	1.7	Pcon+mamL+mamQ(S+P)	2.3	1	5	10
mamB Colony_11_4(X+P)	1.7	Pcon+mamL+mamQ(S+P)	2.3	1	5	10
pSB3T5(E+S)	1.4	Pcon+mamB+His(E+S)	2.6	1	5	10

Transformation

Tatsui

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
9/20 Ligation Pcon+mamL+mamQ+mamB Colony_10_3	1	10	11	LB(CP)
9/20 Ligation Pcon+mamL+mamQ+mamB Colony_10_4	1	10	11	LB(CP)
9/20 Ligation Pcon+mamL+mamQ+mamB Colony_11_3	1	10	11	LB(CP)
9/20 Ligation Pcon+mamL+mamQ+mamB Colony_11_4	1	10	11	LB(CP)
9/20 Ligation Pcon+mamB+His	1	10	11	LB(TET)

9/22

Colony PCR

Tatsui

NameⅠ	NameⅡ	NameⅢ	NameⅣ
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_1	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_1	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_1	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_1
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_2	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_2	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_2
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_3	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_3	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_3	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_3
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_4	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_4	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_4	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_4
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_5	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_5	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_5	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_5
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_6	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_6	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_6	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_6
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_7	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_7	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_7	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_7
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_8	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_8	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_8	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_8

NameⅤ	NameⅥ
9/20 Transformation Pcon+mamB+His Colony_1	9/19 Transformation Pcon+mamB+His Colony_1
9/20 Transformation Pcon+mamB+His Colony_2	9/19 Transformation Pcon+mamB+His Colony_2
9/20 Transformation Pcon+mamB+His Colony_3	9/19 Transformation Pcon+mamB+His Colony_3
9/20 Transformation Pcon+mamB+His Colony_4	-
9/20 Transformation Pcon+mamB+His Colony_5	-

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ	Colony PCR ProductsⅡ
1	Pcon+mamL+mamQ+mamB Colony_10_3_1	Pcon+mamL+mamQ+mamB Colony_11_3_1
2	Pcon+mamL+mamQ+mamB Colony_10_3_2	Pcon+mamL+mamQ+mamB Colony_11_3_2
3	Pcon+mamL+mamQ+mamB Colony_10_3_3	Pcon+mamL+mamQ+mamB Colony_11_3_3
4	Pcon+mamL+mamQ+mamB Colony_10_3_4	Pcon+mamL+mamQ+mamB Colony_11_3_4
5	Pcon+mamL+mamQ+mamB Colony_10_3_5	Pcon+mamL+mamQ+mamB Colony_11_3_5
6	Pcon+mamL+mamQ+mamB Colony_10_3_6	Pcon+mamL+mamQ+mamB Colony_11_3_6
7	Pcon+mamL+mamQ+mamB Colony_10_3_7	Pcon+mamL+mamQ+mamB Colony_11_3_7
8	Pcon+mamL+mamQ+mamB Colony_10_3_8	Pcon+mamL+mamQ+mamB Colony_11_3_8
9	100b ladder	100b ladder
10	Pcon+mamL+mamQ+mamB Colony_10_4_1	Pcon+mamL+mamQ+mamB Colony_11_4_1
11	Pcon+mamL+mamQ+mamB Colony_10_4_2	Pcon+mamL+mamQ+mamB Colony_11_4_2
12	Pcon+mamL+mamQ+mamB Colony_10_4_3	Pcon+mamL+mamQ+mamB Colony_11_4_3
13	Pcon+mamL+mamQ+mamB Colony_10_4_4	Pcon+mamL+mamQ+mamB Colony_11_4_4
14	Pcon+mamL+mamQ+mamB Colony_10_4_5	Pcon+mamL+mamQ+mamB Colony_11_4_5
15	Pcon+mamL+mamQ+mamB Colony_10_4_6	Pcon+mamL+mamQ+mamB Colony_11_4_6
16	Pcon+mamL+mamQ+mamB Colony_10_4_7	Pcon+mamL+mamQ+mamB Colony_11_4_7
17	Pcon+mamL+mamQ+mamB Colony_10_4_8	Pcon+mamL+mamQ+mamB Colony_11_4_8

Ligation

No Name

Insert/(µL)		Vector/(µL)		T4 Ligase/(µl)	10*Buffer/(µl)	MilliQ/(µl)	Total/(µl)
mamB Colony_10_3(X+P)	1	Pcon+mamL+mamQ(S+P)	7.5	0.5	1	0	10

Restriction Enzyme Digestion

Tatsui

Sample	DNA/(µl)	EcoR1/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	Buffur/(µl)	CLAP/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/19 Miniprep Pcon+mamL+mamQ+pSB1C3	34.8	0	0	2	2	0.8	8(B)	1	31.4	80

Colony PCR

Honda

NameⅠ	NameⅡ	NameⅢ	NameⅣ
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_1	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_1	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_1	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_1
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_2	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_2	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_2
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_3	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_3	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_3	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_3
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_4	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_4	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_4	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_4
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_5	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_5	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_5	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_5
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_6	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_6	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_6	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_6
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_7	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_7	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_7	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_7
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_3_8	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_10_4_8	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_8	9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_4_8

NameⅤ
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2(VF+VR)
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2(seq_4+VR)
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2(L_F+B_R)
9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2(Q_F+B_R)

Electrophoresis

Tatsui

Lane	Colony PCR ProductsⅠ	Colony PCR ProductsⅡ	Colony PCR ProductsⅢ
1	Pcon+mamL+mamQ+mamB Colony_10_3_1	Pcon+mamL+mamQ+mamB Colony_11_3_1	-
2	Pcon+mamL+mamQ+mamB Colony_10_3_2	Pcon+mamL+mamQ+mamB Colony_11_3_2	-
3	Pcon+mamL+mamQ+mamB Colony_10_3_3	Pcon+mamL+mamQ+mamB Colony_11_3_3	-
4	Pcon+mamL+mamQ+mamB Colony_10_3_4	Pcon+mamL+mamQ+mamB Colony_11_3_4	-
5	Pcon+mamL+mamQ+mamB Colony_10_3_5	Pcon+mamL+mamQ+mamB Colony_11_3_5	-
6	Pcon+mamL+mamQ+mamB Colony_10_3_6	Pcon+mamL+mamQ+mamB Colony_11_3_6	-
7	Pcon+mamL+mamQ+mamB Colony_10_3_7	Pcon+mamL+mamQ+mamB Colony_11_3_7	-
8	Pcon+mamL+mamQ+mamB Colony_10_3_8	Pcon+mamL+mamQ+mamB Colony_11_3_8	-
9	100b ladder	100b ladder	100b ladder
10	Pcon+mamL+mamQ+mamB Colony_10_4_1	Pcon+mamL+mamQ+mamB Colony_11_4_1	9/19 Transformation Pcon+mamB+His Colony_1
11	Pcon+mamL+mamQ+mamB Colony_10_4_2	Pcon+mamL+mamQ+mamB Colony_11_4_2	9/19 Transformation Pcon+mamB+His Colony_2
12	Pcon+mamL+mamQ+mamB Colony_10_4_3	Pcon+mamL+mamQ+mamB Colony_11_4_3	9/19 Transformation Pcon+mamB+His Colony_3
13	Pcon+mamL+mamQ+mamB Colony_10_4_4	Pcon+mamL+mamQ+mamB Colony_11_4_4	Pcon+mamL+mamQ+mamB Colony_11_3_2(VF+VR)
14	Pcon+mamL+mamQ+mamB Colony_10_4_5	Pcon+mamL+mamQ+mamB Colony_11_4_5	Pcon+mamL+mamQ+mamB Colony_11_3_2(seq_4+VR)
15	Pcon+mamL+mamQ+mamB Colony_10_4_6	Pcon+mamL+mamQ+mamB Colony_11_4_6	Pcon+mamL+mamQ+mamB Colony_11_3_2(L_F+B_R)
16	Pcon+mamL+mamQ+mamB Colony_10_4_7	Pcon+mamL+mamQ+mamB Colony_11_4_7	Pcon+mamL+mamQ+mamB Colony_11_3_2(Q_F+B_R)
17	Pcon+mamL+mamQ+mamB Colony_10_4_8	Pcon+mamL+mamQ+mamB Colony_11_4_8	-

Miniprep

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
Pcon+mamQ+pSB1C3 Colony_3	85	1.51	0.79
Pcon+mamQ+pSB1C3 Colony_5	60	1.94	1.12

9/27

Western Blotting

Honda

Make the 20% acrilamid gel apray the following

Lane	Sample
1-5 9-12	Sample buffer
6	T7-RBS-pSB1C3(control)
7	pL(pSB1C3)
8	protein marker

Electrophoresis:200V 25mA 30min

Transcription:50V 200mA 73min

Liquid Culture

Sample
pLQB(9/22 master)
pLQ(9/22 master)

9/28

Fixation

Honda

25% Glyceraldehyde/(ml)	Phosphate buffer/(ml)	MilliQ/(ml)	Total/(ml)
1.25	5.0	3.75	10.0

9/29

Liquid Culture

Honda

Sample
9/22 master pLQB
9/22 master pLQ
9/22 master pL
9/22 master pQ-3
9/22 master pQ-5
9/20 master pB-22
9/20 master pB-23

Fixation

Honda

Osmic acid/(ml)	Phosphate buffer/(ml)	Total/(ml)
4	4	8

9/30

Miniprep

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
9/29 Liquid Culture pLQB	-	-	-
9/29 Liquid Culture pLQ	-	-	-

Western Blotting

Honda

Make the 20% acrilamid gel apray the following

Lane	Sample
2	Marker
3	pLQB
4	pLQ
5	pL
6	pQ-3
7	pQ-5
8	pB
9	GTP-His
10	T7-RBS-pSB1C3(control)
11	Sample buffer

Electrophoresis:200V 25mA 1h30min

Transcription:50V 200mA 73min

Liquid Culture

Honda

Sample
9/22 master pLQB
9/22 master pQ(3)

10/1

Ethanol Precipitation

Tatsui

Sample
9/28 pL(pSB1C3)(VF)(Miniprep product)
9/28 pL(pSB1C3)(VR)(Miniprep product)
9/22 pB(22)(VF)(Miniprep product)
9/22 pB(22)(VR)(Miniprep product)
9/22 pB(23)(VF)
9/22 pB(23)(VR)
10/1 pQ(3)(VF)(Miniprep product)
10/1 pQ(3)(VR)(Miniprep product)
10/1 pLQB(VF)(Miniprep product)
10/1 pLQB(seq-1)(Miniprep product)
10/1 pLQB(seq-2)(Miniprep product)
10/1 pLQB(seq-3)(Miniprep product)
10/1 pLQB(seq-4)(Miniprep product)
10/1 pLQB(VR)(Miniprep product)

Liquid Culture

Honda

Sample
9/22 master Plate pLQB
9/22 master Plate pQ(3)

Restriction Enzyme Digestion

Sample	DNA/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	BSA	Buffer/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/23 pQ	30	3	0	3	1	9	44	90
pQ(control)	1	0	0	0	0	1	8	10
9/2 Pcon(pSB1C3)	30	0	3	3	1	9	44	90
9/2 Pcon(pSB1C3)(control)	1	0	0	0	0	1	8	10

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
9/29 Liquid Culture pLQB	-	-	-
9/29 Liquid Culture pQ(3)	-	-	-
9/29 Liquid Culture pQ(22)	-	-	-
9/29 Liquid Culture pQ(23)	-	-	-

Sequence PCR

Target	9/28 pL(pSB1C3)(VF)(Miniprep product)	9/28 pL(pSB1C3)(VR)(Miniprep product)	9/22 pB(22)(VF)(Miniprep product)	9/22 M pB(22)(VR)	9/22 pB(23)(VF)	9/22 pB(23)(VR)	10/1 M pQ(3)(VF)	10/1 M pQ(3)(VR)	10/1 M pLQB(VF)	10/1 M pLQB(seq-1)	10/1 M pLQB(seq-2)	10/1 M pLQB(seq-3)	10/1 M pLQB(seq-4)	10/1 M pLQB(VR)
Template/(µl)	4.7	4.7	1.6	1.6	3.2	3.2	5	5	5	5	5	5	5	5
Big dye/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75
Primer(VF)/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5
MilliQ/(µl)	3.05	3.05	6.15	6.15	4.55	4.55	2.75	2.75	2.75	2.75	2.75	2.75	2.75	2.75
TOTAL/(µl)	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5

Steps	Temparature	Time	cycle
Pre Denature	96℃	2min	1time
Denature	96℃	10sec	30cycle
Annealing	55℃	5sec	30cycle
Extension	60℃	4min	30cycle
Final elongation	4℃	1min	1time
Final hold	4℃	infinity	-

Gel Extraction

(1)

Lane	SampleⅠ	Volume/(µl)
1	blank	-
2	1400b ladder	-
3	His-OE-1	-
4	1kb ladder	-
5	750b ladder	-
6	His-OE-2	-

(2)

Lane	SampleⅡ	Volume/(µl)
3,6	pQ(X,P)	-
4	100b ladder	-

(3)

Lane	SampleⅢ	Volume/(µl)
3,6	Pcon pSB1C3(S,P)	-
4	1kb ladder	-

(4)

Lane	SampleⅣ	Volume/(µl)
3	DiDECARB-4	-
6	DiDECARB-5	-
2	DiDECARB-4(control)	-
5	DiDECARB-5(control)	-
4	1kb ladder	-

10/2

Miniprep

DNA	Concentration/(µg/ml)	260/280	260/230
pLQB	390	1.70	1.20
pLQ	319	1.64	0.92
j04450	255	1.59	1.04

10/3

PCR

Honda

Target	Volume
10×buffur for KOD Plus Ver.2/(µl)	5
2mMdNTPs/(µl)	5
25mM MgSO4/(µl)	3
VF Primer/(µl)	1.5
VR Primer/(µl)	1.5
template/(µl)	1
KOD-plus/(µl)	1
MilliQ/(µl)	33
TOTAL/(µl)	50

DNA Purification

DNA	Concentration/(µg/ml)	260/280	260/230
10/3 PB	39.8	1.75	0.92

Digestion

Sample	DNA/(µl)	EcoRI/(µl)	Spe1/(µl)	BSA	Buffer/(µl)	MilliQ/(µl)	TOTAL/(µl)
10/3 Column pB	15.8	1	1	0.2	2	-	20

Restriction Enzyme Digestion

Honda

Sample	DNA/(µl)	Xba1/(µl)	Pst1/(µl)	BSA	Buffer/(µl)	MilliQ/(µl)	TOTAL/(µl)
DiDECARB-4	10	2	2	0.4	4	21.6	40
DiDECARB-4(control)	1	0	0	0	1	8	10
DiDECARB-5	10	2	2	0.4	4	21.6	40
DiDECARB-5(control)	1	0	0	0	1	8	10

Gel Extraction

Tatsui

DNA	Concentration/(µg/ml)	260/280	260/230
pSB1C3(X,P)-4	942	1.89	1.26
pSB1C3(X,P)-5	518	1.87	1.26

10/4

Digestion

Tatsui

Sample	DNA/(µl)	Xba1/(µl)	Pst1/(µl)	BSA	Buffer/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/18 MP pL-pSB1C3(85)	24	1	1	0.4	4	9.6	40
9/18 MP pL-pSB1C3(85)(control)	1	0	0	0	1	8	10
9/18 MP Bµ-pSB1C3-11-3(355)	6	1	1	0.4	4	27.6	40
9/18 MP Bµ-pSB1C3-11-3(355)(control)	1	0	0	0	1	8	10

Gel Extraction

(1)

Lane	SampleⅠ	Volume/(µl)
1	10/4 Bµ pSB1C3-11-3(control)	-
3,4	10/4 Bµ pSB1C3-11-3(XP)	-
6	ladder	-

(2)

Lane	SampleⅡ	Volume/(µl)
1	ladder	-
3,4	10/4 pL-pSB1C3(XP)	-
6	10/4 pL-pSB1C3(control)	-

Ligation

No name

Sample	Vector/(µL)	Insert/(µL)	Ligase/(µl)	Buffer/(µl)	MilliQ/(µl)	Total/(µl)
9/20 Q-pSB1C3(B)	1	3	1	5	0	10
9/16 Q-pSB1C3(B)	1	3	1	5	0	10
9/20 Q-pSB1C3(B)(control)	1	0	1	5	3	10
9/16Q-pSB1C3(B)(control)	1	0	1	5	3	10

Transformation

Sample	Plasmid/(µl)	CompetentCells(DH5α)/(µl)
E1	2	10
E2	2	10
E3	2	10
E4	2	10

10/5

Ethanol Precipitation

Honda

10/3 Gel Extraction PconpSB1C3(SP)

Ligation

Honda

sample	Vector/(µL)	Insert/(µL)	Toyobo Ligation high/(µl)
10/5 PconpSB1C3(SP)+9/20pQ(3)(XP)	1	1	2
10/5 PconpSB1C3(SP)(control)	1	1	2

Transformation

Honda

Sample	Plasmid/(µl)	CompetentCells(DH5α)/(µl)
F1	2	10
F2	2	10

Colony PCR

Lane	Colony PCR ProductsⅠ
9-14	E1 1-6
15-20	E2 1-6

Liquid Culture

Sample
E1 1-6
E2 1-6

DNA Purification

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
pB PCR	57	2.06	2.39

Digestion

Sample	DNA/(µl)	EcoRI/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	Buffer/(µl)	BSA	MilliQ/(µl)	TOTAL/(µl)
9/18 MP Bµ(pSB1C3)11-4(ES)	10	1	0	1	0	4	0.4	23.6	40
9/18 MP Bµ(pSB1C3)11-4(control)	1	0	0	0	0	1	0	8	10
9/22 MP pQ-3(XP)	40	0	4	0	4	16	1.6	94.4	160
9/22 MP pQ-3(control)	1	0	0	0	0	1	0	8	10
9/22 Pcon Master(SP)	10	0	0	1	1	4	0.4	23.6	40
9/22 Pcon Master(control)	1	0	0	0	0	1	0	8	10
9/22 pB(PCR Product)(ES)	20	1	0	1	0	4	0.4	13.6	40
9/22 pB(PCR Product)(control)	1	0	0	0	10/td>	1	0	8	10

PCR

No Name

Target	Volume
2×KAPA HiFi Hotstart Ready Mix/(µl)	12.5
Fw Primer/(µl)	0.75
Rv Primer/(µl)	0.75
Template(9/22 Mini Pcon-mamQ-3)	pick up
MilliQ/(µl)	11
TOTAL/(µl)	25

Steps	Temparature	Time	cycle
Pre Denature	98℃	5min	1time
Denature	98℃	20sec	30cycle
Annealing	60℃	15sec	30cycle
Extension	72℃	30sec	30cycle
Final elongation	72℃	5min	1time
Final hold	12℃	-	-

10/6

Sequence PCR

Target	10/6 T7-RBS-his(pSB1C3)-1-VF(Miniprep product)	10/6 T7-RBS-his(pSB1C3)-1-VR(Miniprep product)	10/6 T7-RBS-his(pSB1C3)-2-VF(Miniprep product)	10/6 T7-RBS-his(pSB1C3)-2-VR(Miniprep product)	10/6 T7-RBS-his(pSB1C3)-3-VF(Miniprep product)	10/6 T7-RBS-his(pSB1C3)-3-VR(Miniprep product)	10/6 Q(pSB1C3)E1-1 VF(Miniprep product)	10/6 Q(pSB1C3)E1-1 VR(Miniprep product)	10/6 M Q(pSB1C3)E1-2-VF	10/6 Q(pSB1C3)E1-2-VR(Miniprep product)	10/6 M Q(pSB1C3)E1-3-VF	10/6 M Q(pSB1C3)E1-3-VR	10/6 M Q(pSB1C3)E2-1-VF	10/6 M Q(pSB1C3)E2-1-VR	10/6 Q(pSB1C3)E2-2-VF(Miniprep product)	10/6 Q(pSB1C3)E2-2-VR(Miniprep product)
Template/(µl)	2.2	2.2	2.5	2.5	2.5	2.5	1.85	1.85	1.1	1.1	1.7	1.7	1.8	1.8	1.7	1.7
Big dye/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5
5×Buffer/(µl)	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75	1.75
Primer/(µl)	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5
MilliQ/(µl)	5.55	5.55	5.25	5.25	5.25	5.25	5.9	5.9	6.65	6.65	6.05	6.05	5.95	5.95	6.05	6.05
TOTAL/(µl)	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5	10.5

Steps	Temparature	Time	cycle
Pre Denature	96℃	2min	1time
Denature	96℃	10sec	30cycle
Annealing	50℃	5sec	30cycle
Extension	60℃	4min	30cycle
Final elongation	4℃	1min	1time
Final hold	4℃	infinity	-

Miniprep

DNA	Concentration/(µg/ml)	260/280	260/230
T7-RBS-his(pSB1C3)-1	180	1.84	1.76
T7-RBS-his(pSB1C3)-2	160	1.92	1.92
T7-RBS-his(pSB1C3)-3	156	1.69	1.64
E1-1	216	1.84	2.04
E1-2	355	1.82	2.31
E1-3	238	1.81	2.11
E2-1	225	1.83	2.00
E2-2	230	1.76	1.84

Gel Extraction

(1)

Lane	SampleⅠ	Volume/(µl)
1	10/5 B&micro(pSB1C3)(control)	-
3	10/5 B&micro(pSB1C3)(ES)	-
6	10/5 pB(ES)	-

(2)

Lane	SampleⅡ	Volume/(µl)
1	pQ-3(control)	-
3	pQ-3(XP)	-
4	Pcon(control)	-
6	Pcon(SP)	-

10/7

Liquid Culture

Sample
pLQB(9/22)
pLQ(9/22)
pL(9/22)
control(T7-RBS)(9/18)

10/8

Ligation

Honda

sample	Insert/(µL)	Vector/(µL)	2x Ligation high/ (µl)	MilliQ	TOTAL
pQ pSB1C3	1	1	2	0	4
pQ pSB1C3(control)	0	1	2	1	4
pB pSB1C3	1	1	2	0	4
pB pSB1C3(control)	0	1	2	1	4

Liquid Culture

Sample
9/22 pLQB
9/22 pLQ
9/22 pL
9/18 control(T7-RBS)(9/18)

Inoculation

Sample
10/7 pLQB
10/7 pLQ
10/7 pL
10/7 control

16:30

Sample	Absorbance
BL21	0.224
LQB	0.031
LQ	0.061

17:30

Sample	Absorbance
BL21	0.720
LQB	0.057
LQ	0.139

18:00

Sample	Absorbance
LQ	0.088
LQB	0.211

18:30

Sample	Absorbance
LQ	0.267
LQB	0.122

19:30

Sample	Absorbance
LQB	0.216
LQ	0.412

10/9 13:30

Sample	Absorbance
LQB(morning)	1.657
LQ	1.625
LQB(evening)	1.014
-	0.064
LQ	1.652
L	2.117
control	2.124

10/9

Colony PCR

Target	Volume
2x quick tag/(µl)	15
VF Primer/(µl)	0.6
VR Primer/(µl)	0.6
MilliQ/(µl)	13.8
TOTAL/(µl)	30

Steps	Temparature	Time	cycle
Pre Denature	94℃	2min	1time
Denature	94℃	30sec	30cycle
Annealing	55℃	30sec	30cycle
Extension	68℃	1min	30cycle
Final elongation	68℃	7min	1time
Final hold	4℃	infinity	-

Transformation

Sample	Plasmid/(µl)	CompetentCells(DH5α)/(µl)	TOTAL/(µl)
pQ	2	20	22
pB	2	20	22
pQ(control)	2	20	22
pB(control)	2	20	22

Inoculation

Sample
10/8 pLQB
10/8 pLQ
10/8 pL
10/8 control

14:00

Sample	Absorbance
LQB	0.177
LQ	0.306
L	0.477
control	0.435

14:30

Sample	Absorbance
LQB	0.240
LQ	0.351
L	0.641
control	0.640

15:00

Sample	Absorbance
LQB	0.351
LQ	0.395

15:30

Sample	Absorbance
LQB	0.413
LQ	0.397

16:00

Sample	Absorbance
LQB	0.564
LQ	0.458

16:30

Sample	Absorbance
LQB	0.732
LQ	0.518

17:00

Sample	Absorbance
LQ	0.581

17:30

Sample	Absorbance
LQ	0.458

18:00

Sample	Absorbance
LQ	0.749

10/10

Electrophoresis

Honda

Lane	PCR Product
1	1kb ladder
2	10/9 pB(pSB1C3) Colony_1
3	10/9 Negative Control

Restriction Enzyme Digestion

Honda

Sample	DNA/(µl)	EcoR1/(µl)	Pst1/(µl)	Buffur/(µl)	BSA/(µl)	MilliQ/(µl)	TOTAL/(µl)
9/15 pLQ	5	0.5	0.5	2(H)	0.5	11.5	20
10/2 pLQB	7	1	1	4(H)	0.5	26.5	40
10/2 pLQB(Nega)	1	0	0	1(H)	0	8	10
9/2 pSB4A5	10	1	1	4(H)	0.5	26.5	40
9/2 pSB4A5(Nega)	1	0	0	1(H)	0	8	10

20:00~ O/N

Liquid Culture

Honda

Name	medium
10/6 Transformation Pcon+mamB+pSB1C3 Colony_1	LB medium(CP)*2
9/22 Master Plate Pcon+mamL+mamQ	LB medium(CP)*2

Miniprep

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
10/10 Liquid culture Pcon+mamB colony_1	74	1.70	3.82
10/10 Liquid culture Pcon+mamL+mamQ	59	1.88	5.10

Gel Extraction

Honda

Lane	SampleⅠ	Volume/(µl)
2	10/10 Pcon+mamL+mamQ+mamB (Nega)	5
4	10/10 Pcon+mamL+mamQ+mamB (E+P)	35
7	10/10 Pcon+mamL+mamQ (E+P)	20
10	10/10 pSB4A5 (Nega)	5
12	10/10 pSB4A5 (E+P)	35
14	1kb ladder	3

10/13

Restriction Enzyme Digestion

Honda

Sample	DNA/(µl)	EcoR1/(µl)	Xba1/(µl)	Spe1/(µl)	Pst1/(µl)	Buffur/(µl)	BSA/(µl)	MilliQ/(µl)	CIAP/(µl)
TOTAL/(µl)
10/11 Miniprep Pcon+mamL+mamQ	23	1	0	0	1	4(H)	0.5	11.5	1	41
10/11 Miniprep Pcon+mamL+mamQ(Nega)	1	0	0	0	0	1(H)	0	8	0	10

11:00~ 2hours

DNA Purification

Honda

DNA	Concentration/(µg/ml)	260/280	260/230
10/13 Digestion Pcon+mamL+mamQ(E+P)	59	1.79	-0.66

Ligation

Honda

Insert/(µL)		Vector/(µL)		2*Ligation high/(µl)	Total/(µl)
10/13 Pcon+mamL+mamQ (E+P)	2	10/11 pSB4A5 (E+P)(2 fold dilution)	2	4	8
10/11 Pcon+mamL+mamQ+mamB(E+P)	2	10/11 pSB4A5 (E+P)(2 fold dilution)	2	4	8

Transformation

Honda

Sample/(µL)		CompetentCells/(µl)	Total/(µl)	Medium
10/10 Ligation Pcon+mamL+mamQ+pSB4A5	6	30(2/23)	36	LB(CP)
10/10 Ligation Pcon+mamL+mamQ+mamB+pSB4A5	6	30(2/23)	36	LB(CP)

10/14

Liquid Culture

Honda

Name	medium
9/22 Master Plate Pcon+mamL+mamQ+mamB	LB medium(CP)
9/22 Master Plate Pcon+mamL+mamQ	LB medium(CP)
9/22 Master Plate Pcon+mamL	LB medium(CP)
10/6 Transformation Pcon+ mamB	LB medium(CP)
10/9 Transformation Pcon+ mamB	LB medium(CP)
10/4 Transformation mamQ+pSB1C3 (E1-3)	LB medium(CP)
9/18 Master Plate T7+RBS+pSB1C3	LB medium(CP)
10/13 Master Plate Pcon+mamL+mamQ+pSB4A5	LB medium(Amp)

10/15

Inoculation

Honda

10:45~

Sample
10/14 pLQB
10/14 pLQ
10/14 pL
10/14 T7-RBS
10/14 pLQ(4A5)

12:30

Sample	Absorbance
LQB	0.096
LQ	0.087
L	0.278
T7-RBS	0.253

13:05

Sample	Absorbance
LQB	0.153
LQ	0.139
L	0.448
T7-RBS	0.389
pLQ(4A5)	0.277

13:46

Sample	Absorbance
LQB	0.275
LQ	0.204
L	0.597
T7-RBS	0.516
pLQ(4A5)	0.443

14:26

Sample	Absorbance
LQB	0.293
LQ	0.275
L	0.896
T7-RBS	0.595
pLQ(4A5)	0.641

14:55

Sample	Absorbance
LQB	0.435
LQ	0.434
L	0.914
T7-RBS	0.837
pLQ(4A5)	0.863

15:43

Sample	Absorbance
LQB	0.871
LQ	0.826
L	1.735
T7-RBS	1.692
pLQ(4A5)	1.458

16:33

Sample	Absorbance
LQB	1.112
LQ	1.046
L	0.747
T7-RBS	1.819
pLQ(4A5)	1.642

17:15

Sample	Absorbance
LQB	1.725
LQ	1.613
L	2.188
T7-RBS	2.123
pLQ(4A5)	2.007

18:20

Sample	Absorbance
LQB	1.833
LQ	1.712
L	2.194
T7-RBS	2.205
pLQ(4A5)	2.127

18:45

Sample	Absorbance
LQB	1.928
LQ	1.808
L	2.224
T7-RBS	2.233
pLQ(4A5)	2.148

Colony PCR

Honda

NameⅠ	NameⅡ
10/6 Pcon+mamB+pSB1C3 colony_1	10/13 Pcon+mamL+mamQ+pSB4A5 colony_1(seq-2+VR)
10/9 Pcon+mamB+pSB1C3 colony_1	10/13 Pcon+mamL+mamQ+pSB4A5 colony_2(seq-2+VR)
10/13 Pcon+mamL+mamQ+pSB4A5 colony_1	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1(seq-2+VR)
10/13 Pcon+mamL+mamQ+pSB4A5 colony_2	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2(seq-2+VR)
10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3(seq-2+VR)
10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4(seq-2+VR)
10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3	-
10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4	-

10/16

Electrophoresis

Honda

Lane	Colony PCR Products
6	1kbp ladder
7	10/6 Pcon+mamB+pSB1C3 colony_1
8	10/6 Pcon+mamB+pSB1C3 colony_2
9	10/13 Pcon+mamL+mamQ+pSB4A5 colony_1
10	10/13 Pcon+mamL+mamQ+pSB4A5 colony_2
11	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1
12	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2
13	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3
14	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4
15	10/13 Pcon+mamL+mamQ+pSB4A5 colony_1(seq-2+VR)
16	10/13 Pcon+mamL+mamQ+pSB4A5 colony_2(seq-2+VR)
17	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1(seq-2+VR)
18	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2(seq-2+VR)
19	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3(seq-2+VR)
20	10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4(seq-2+VR)

Inoculation

Honda

15:15~

Sample
10/15 RFP-his

17:15

Sample	Absorbance
RFP-his	0.354

18:50

Sample	Absorbance
RFP-his	0.908

19:20

Sample	Absorbance
RFP-his	0.992

10/17

Western Blotting

Honda

Make the 20% acrilamid gel apray the following

Lane	Sample	Volume/(µl)
2	Sample buffer	5
3	protein marker	5
4	10/14 Pcon+mamL+mamQ+mamB+pSB1C3	5
5	10/14 Pcon+mamL+mamQ+pSB1C3	5
6	10/14 Pcon+mamB+pSB1C3	5
7	10/14 Pcon+mamL+pSB1C3	5
9	10/14 T7+RBS+pSB1C3(Nega)	5
10	GFP-his(protein)(10 fold dilution)	5
11	GFP-his(protein)(10 fold dilution)(37°C denature for 10 min.)	5

Electrophoresis:200V 25mA 90min

Transcription:50V 200mA 73min

@@ Line 1: / Line 1: @@
 <html>
-<div id="kyoto-notebook">
+<div class="kyoto-notebook">
 <div>
@@ Line 6: / Line 6: @@
 <h3>7/15</h3>
 <h4>Transformation</h4>
-<span class="author">Tatsui, Matsumoto and Sukegawa</span>
+<p><span class="kyoto-author">Tatsui, Matsumoto and Sukegawa</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 18: / Line 18: @@
 <h3>7/16</h3>
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 32: / Line 32: @@
 <h3>7/17</h3>
 <h4>Colony PCR</h4>
-<span class="author">Tatsui, Matsumoto, Li, and Yamauchi</span>
+<p><span class="kyoto-author">Tatsui, Matsumoto, Li, and Yamauchi</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th></tr>
@@ Line 46: / Line 46: @@
 <h4>Liquid Culture</h4>
-<span class="author">Tatsui, Matsumoto, Li, and Yamauchi</span>
+<p><span class="kyoto-author">Tatsui, Matsumoto, Li, and Yamauchi</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 68: / Line 68: @@
 <h3>7/18</h3>
 <h4>Miniprep</h4>
-<span class="author">Tatsui, Matsumoto, Tsujii, Stephane, and Yamauchi</span>
+<p><span class="kyoto-author">Tatsui, Matsumoto, Tsujii, Stephane, and Yamauchi</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 84: / Line 84: @@
 <tr><td>7/16 BBa_B0032(2) Colony_3</td><td>194</td><td>1.89</td><td>1.33</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/7/73/Kyoto-0718-Colony-PCR.png">
 </div>
@@ Line 90: / Line 91: @@
 <h3>7/30</h3>
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>BSA/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 99: / Line 100: @@
 <tr><td>7/16 BBa_B0030(2) Colony_1(Nega)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1(M)</td><td>0</td><td>8</td><td>10</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/e/e7/Kyoto-0730-Digestion.png">
 <h4>Electrophoresis</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion Products</td></tr>
@@ Line 117: / Line 119: @@
 <h3>7/31</h3>
 <h4>Transformation</h4>
-<span class="author">Hashitani, Tatsui, Li and Yamauchi</span>
+<p><span class="kyoto-author">Hashitani, Tatsui, Li and Yamauchi</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 125: / Line 127: @@
 <h4>Liquid Culture</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 137: / Line 139: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Hashitani, Tatsui, Li and Yamauchi</span>
+<p><span class="kyoto-author">Hashitani, Tatsui, Li and Yamauchi</span></p>
 <table>
 <tr><th>7/18 RBS Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>BSA/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 152: / Line 154: @@
 <h3>8/1</h3>
 <h4>Electrophoresis</h4>
-<span class="author">Honda, Li and Yamauchi</span>
+<p><span class="kyoto-author">Honda, Li and Yamauchi</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion Products</td></tr>
@@ Line 164: / Line 166: @@
 <tr><td>8</td><td>7/31 BBa_B0032(Nega)</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/9/94/Kyoto-0801-Digestion.png">
 <h4>PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>BBa_E0240(RBS-GFP-DT)</th><th>Volume</th></tr>
@@ Line 193: / Line 196: @@
 <tr><td>Product</td><td>80</td><td>1.91</td><td>1.78</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/0/06/Kyoto-0801-PCR.png">
 </div>
@@ Line 199: / Line 203: @@
 <h3>8/2</h3>
 <h4>Miniprep</h4>
-<span class="author">Tatsui, Honda, Matsumoto, Yamauchi, Li, Tsujii, and Nakamura</span>
+<p><span class="kyoto-author">Tatsui, Honda, Matsumoto, Yamauchi, Li, Tsujii, and Nakamura</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 215: / Line 219: @@
 <h3>8/20</h3>
 <h4>Transformation</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 227: / Line 231: @@
 <h3>8/21</h3>
 <h4>Colony PCR</h4>
-<span class="author">Shimazaki</span>
+<p><span class="kyoto-author">Shimazaki</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 237: / Line 241: @@
 <h4>Electrophoresis</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Lane</th><th>PCR Product</th></tr>
@@ Line 248: / Line 252: @@
 <h4>Liquid Culture</h4>
-<span class="author">Honda and Tatsui</span>
+<p><span class="kyoto-author">Honda and Tatsui</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 258: / Line 262: @@
 <div>
-<a name="0821" class="kyoto-jump"></a>
+<a name="0822" class="kyoto-jump"></a>
 <h3>8/22</h3>
 <h4>Miniprep</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 270: / Line 274: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Nakamura</span>
+<p><span class="kyoto-author">Nakamura</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 279: / Line 283: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui and Yamauchi</span>
+<p><span class="kyoto-author">Tatsui and Yamauchi</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 290: / Line 294: @@
 <h3>8/25</h3>
 <h4>Transformation</h4>
-<span class="author">Tatsui, Kita and Li</span>
+<p><span class="kyoto-author">Tatsui, Kita and Li</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 298: / Line 302: @@
 <h4>Liquid Culture</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 309: / Line 313: @@
 <h3>8/26</h3>
 <h4>Miniprep</h4>
-<span class="author">Tsujii, Honda and Matsumoto</span>
+<p><span class="kyoto-author">Tsujii, Honda and Matsumoto</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 316: / Line 320: @@
 <h4>Liquid Culture</h4>
-<span class="author">Tatsui, Matsumoto and Nakamura</span>
+<p><span class="kyoto-author">Tatsui, Matsumoto and Nakamura</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 328: / Line 332: @@
 <h3>8/27</h3>
 <h4>Miniprep</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 336: / Line 340: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 347: / Line 351: @@
 <h3>8/28</h3>
 <h4>Liquid Culture</h4>
-<span class="author">Yamauchi</span>
+<p><span class="kyoto-author">Yamauchi</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 358: / Line 362: @@
 <h3>8/29</h3>
 <h4>Miniprep</h4>
-<span class="author">Matsumoto</span>
+<p><span class="kyoto-author">Matsumoto</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 365: / Line 369: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 387: / Line 391: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 403: / Line 407: @@
 <h4>Liquid Culture</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 416: / Line 420: @@
 <h3>9/2</h3>
 <h4>Miniprep</h4>
-<span class="author">Honda, Yamauchi and Li</span>
+<p><span class="kyoto-author">Honda, Yamauchi and Li</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 425: / Line 429: @@
 <h4>Gel Extraction</h4>
-<span class="author">Matsumoto</span>
+<p><span class="kyoto-author">Matsumoto</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion ProductⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 440: / Line 444: @@
 <tr><td>11</td><td>9/1 pSB2K3 (E+P)(Extraction)</td><td>85</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/ac/Kyoto-0902-Gel-Extraction-No.1-be.png">
+<img src="https://static.igem.org/mediawiki/2014/e/ee/Kyoto-0902-Gel-Extraction-No.1-af.png">
 <table>
@@ Line 453: / Line 459: @@
 <tr><td>9</td><td>9/1 Pcon Colony_1 (Nega)</td><td>10</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/3/31/Kyoto-0902-Gel-Extraction-No.2-be.png">
+<img src="https://static.igem.org/mediawiki/2014/f/f7/Kyoto-0902-Gel-Extraction-No.2-af.png">
 </div>
@@ Line 459: / Line 467: @@
 <h3>9/3</h3>
 <h4>Concentration Measurement</h4>
-<span class="author">Matsumoto, Yamauchi and Li</span>
+<p><span class="kyoto-author">Matsumoto, Yamauchi and Li</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 470: / Line 478: @@
 <h4>Ligation</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 482: / Line 490: @@
 <h4>Transformation</h4>
-<span class="author">Matsumoto</span>
+<p><span class="kyoto-author">Matsumoto</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 498: / Line 506: @@
 <h3>9/4</h3>
 <h4>Colony PCR</h4>
-<span class="author">Honda and Yamauchi</span>
+<p><span class="kyoto-author">Honda and Yamauchi</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th><th>NameⅢ</th><th>NameⅣ</th></tr>
@@ Line 530: / Line 538: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 547: / Line 555: @@
 <h3>9/5</h3>
 <h4>Electrophoresis</h4>
-<span class="author">Honda and Matsumoto</span>
+<p><span class="kyoto-author">Honda and Matsumoto</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 560: / Line 568: @@
 <tr><td>9</td><td>9/4 pSB1C3(Nega) Colony_6</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/8/83/Kyoto-0905-Colony-PCR-No.1.png">
 <table>
@@ Line 573: / Line 582: @@
 <tr><td>9</td><td>9/4 pSB3T5(Nega) Colony_1</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/7/72/Kyoto-0905-Colony-PCR-No.2.png">
 <table>
@@ Line 586: / Line 596: @@
 <tr><td>9</td><td>9/4 pSB2K3(Nega) Colony_4</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/b/bb/Kyoto-0905-Colony-PCR-No.3.png">
 <table>
@@ Line 599: / Line 610: @@
 <tr><td>9</td><td>9/4 Pcon+pSB1C3 Colony_4</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/d/d4/Kyoto-0905-Colony-PCR-No.4.png">
 <table>
@@ Line 611: / Line 623: @@
 <tr><td>8</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/6/64/Kyoto-0905-Colony-PCR-No.5.png">
 <h4>Gel Extraction</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion ProductⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 623: / Line 636: @@
 <tr><td>6</td><td>9/4 pSB2K3(Nega)</td><td>10</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/d/db/Kyoto-0905-Gel-Extraction-No.1-be.png">
+<img src="https://static.igem.org/mediawiki/2014/9/9a/Kyoto-0905-Gel-Extraction-No.1-af.png">
 <table>
@@ Line 633: / Line 648: @@
 <tr><td>6</td><td>9/4 pSB3T5(Nega)</td><td>10</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/7/79/Kyoto-0905-Gel-Extraction-No.2-be.png">
+<img src="https://static.igem.org/mediawiki/2014/3/36/Kyoto-0905-Gel-Extraction-No.2-af.png">
 <table>
@@ Line 643: / Line 660: @@
 <tr><td>6</td><td>9/4 pSB4A5(Nega)</td><td>10</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/b/b0/Kyoto-0905-Gel-Extraction-No.3-be.png">
+<img src="https://static.igem.org/mediawiki/2014/0/07/Kyoto-0905-Gel-Extraction-No.3-af.png">
 <table>
@@ Line 653: / Line 672: @@
 <tr><td>6</td><td>-</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/5/53/Kyoto-0905-Gel-Extraction-No.4-af.png">
 <table>
@@ Line 667: / Line 687: @@
 <h3>9/8</h3>
 <h4>Cloning PCR</h4>
-<span class="author">Honda and Li</span>
+<p><span class="kyoto-author">Honda and Li</span></p>
 <table>
 <tr><th>Target</th><th>mamB</th><th>mamQ</th><th>mamL</th></tr>
@@ Line 687: / Line 707: @@
 <tr><td>Final hold</td><td>4℃</td><td>-</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/b/b9/Kyoto-0908_Cloning_PCR.jpg">
 <h4>Ligation</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 697: / Line 718: @@
 <h4>Electrophoresis</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>Lane</th><th>Cloning PCR Products</td></tr>
@@ Line 708: / Line 729: @@
 <h4>Transformation</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 716: / Line 737: @@
 <h4>Liquid Culture</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 727: / Line 748: @@
 <h3>9/9</h3>
 <h4>DNA Purification</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 736: / Line 757: @@
 <h4>Miniprep</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 743: / Line 764: @@
 <h4>Colony PCR</h4>
-<span class="author">Honda and Li</span>
+<p><span class="kyoto-author">Honda and Li</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 755: / Line 776: @@
 <tr><td>Negative control</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/c/cb/Kyoto-0909_Colony_PCR.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Honda and Li</span>
+<p><span class="kyoto-author">Honda and Li</span></p>
 <table>
 <tr><th>Lane</th><th>Cloning PCR Products</td></tr>
@@ Line 771: / Line 793: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">No name</span>
+<p><span class="kyoto-author">No name</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 785: / Line 807: @@
 <h3>9/10</h3>
 <h4>Gel Extraction</h4>
-<span class="author">Tatsui and Yamaura</span>
+<p><span class="kyoto-author">Tatsui and Yamaura</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion ProductⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 801: / Line 823: @@
 </table>
+<table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
 <tr><td>Pcon(X+P)</td><td>70</td><td>1.40</td><td>0.13</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/3/35/Kyoto-0910_Gel_Extraction_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/a/a1/Kyoto-0910_Gel_Extraction_after.jpg">
 <h4>PCR</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Target</th><th>E+X+RBS+mamB+S</th><th>X+RBS+mamL+His+S+P</th><th>X+RBS+mamQ+His+S+P</th></tr>
@@ Line 816: / Line 841: @@
 <tr><td>TOTAL/(&micro;l)</td><td>25</td><td>25</td><td>25</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/ad/Kyoto-0910_PCR.jpg">
 <table>
@@ Line 828: / Line 854: @@
 <h4>Electrophoresis</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>Lane</th><th>Cloning PCR Products</td></tr>
@@ Line 840: / Line 866: @@
 <h4>DNA Purification</h4>
-<span class="author">Honda and Yamaura</span>
+<p><span class="kyoto-author">Honda and Yamaura</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 849: / Line 875: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Shimizu</span>
+<p><span class="kyoto-author">Shimizu</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 858: / Line 884: @@
 <h4>Ligation</h4>
-<span class="author">Tatsui and Murada</span>
+<p><span class="kyoto-author">Tatsui and Murada</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 868: / Line 894: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui and Murada</span>
+<p><span class="kyoto-author">Tatsui and Murada</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 881: / Line 907: @@
 <h3>9/11</h3>
 <h4>DNA Purification</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 890: / Line 916: @@
 <h4>Electrophoresis</h4>
-<span class="author">Murada</span>
+<p><span class="kyoto-author">Murada</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR Products</td></tr>
 <tr><td></td><td></td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/f/f8/Kyoto-0911_Colony_PCR_No.1.jpg">
 <table>
@@ Line 900: / Line 927: @@
 <tr><td></td><td></td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/1/12/Kyoto-0911_Colony_PCR_No.2.jpg">
 <table>
@@ Line 905: / Line 933: @@
 <tr><td></td><td></td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/ae/Kyoto-0911_Colony_PCR_No.3.jpg">
 <table>
@@ Line 910: / Line 939: @@
 <tr><td></td><td></td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/a5/Kyoto-0911_Colony_PCR_No.4.jpg">
 <table>
@@ Line 915: / Line 945: @@
 <tr><td></td><td></td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/f/f6/Kyoto-0911_Colony_PCR_No.5.jpg">
 <h4>Ligation</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 924: / Line 955: @@
 <h4>Transformation</h4>
-<span class="author">Yamauchi</span>
+<p><span class="kyoto-author">Yamauchi</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 932: / Line 963: @@
 <h4>Liquid Culture</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 945: / Line 976: @@
 <h3>9/12</h3>
 <h4>Colony PCR</h4>
-<span class="author">Yamaura</span>
+<p><span class="kyoto-author">Yamaura</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
 <tr><td></td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/9/91/Kyoto-0912_Colony_PCR%28Yamaura%29.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Yamaura</span>
+<p><span class="kyoto-author">Yamaura</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR Products</td></tr>
@@ Line 959: / Line 991: @@
 <h4>Miniprep</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 968: / Line 1,000: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Yasuda</span>
+<p><span class="kyoto-author">Yasuda</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>BSA</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 977: / Line 1,009: @@
 <h4>Ligation</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 985: / Line 1,017: @@
 <h4>DNA Purification</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 992: / Line 1,024: @@
 <h4>Transformation</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 1,000: / Line 1,032: @@
 <h4>Colony PCR</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th></tr>
@@ Line 1,012: / Line 1,044: @@
 <tr><td>9/11 Transformation mamL+pSB1A2 Colony_8</td><td>9/11 Transformation mamQ+pSB1A2 Colony_6</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/d/de/Kyoto-0912_Colony_PCR%28Li%29.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,029: / Line 1,062: @@
 <h4>Colony PCR</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 1,041: / Line 1,074: @@
 <tr><td>9/11 Transformation mamQ+pSB1A2 Black_1</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/9/9a/Kyoto-0912_Colony_PCR%28Honda%29.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,058: / Line 1,092: @@
 <h4>Liquid Culture</h4>
-<span class="author">Yamauchi</span>
+<p><span class="kyoto-author">Yamauchi</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 1,074: / Line 1,108: @@
 <h3>9/13</h3>
 <h4>Miniprep</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,087: / Line 1,121: @@
 <h4>PCR Labeling and Sequence</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Target</th><th>9/13 mamQ+pSB1A2 Colony_4</th><th>9/13 mamQ+pSB1A2 Colony_5</th><th>9/13 mamQ+pSB1A2 Colony_6</th><th>Pcon+pSB1A2</th><th>9/13 mamQ+pSB1A2 Colony_4</th><th>9/13 mamQ+pSB1A2 Colony_5</th><th>9/13 mamQ+pSB1A2 Colony_6</th></tr>
@@ Line 1,109: / Line 1,143: @@
 <h4>Gel Extraction</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion ProductⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,130: / Line 1,164: @@
 <tr><td>9/12 Digestion Pcon+pSB1C3(S+P)</td><td>150</td><td>1.25</td><td>0.71</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/5/53/Kyoto-0913_Gel_Extraction_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/d/dc/Kyoto-0913_Gel_Extraction_after.jpg">
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>BSA</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,142: / Line 1,178: @@
 <h4>Ligation</h4>
-<span class="author">Yasuda</span>
+<p><span class="kyoto-author">Yasuda</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 1,149: / Line 1,185: @@
 <h4>Miniprep</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,160: / Line 1,196: @@
 <h3>9/14</h3>
 <h4>Gel Extraction</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion ProductⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,175: / Line 1,211: @@
 <tr><td>11</td><td>9/13 mamQ Colony_6(X+P)</td><td>15</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/f/ff/Kyoto-0914_Gel_Extraction_No.1_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/a/a1/Kyoto-0914_Gel_Extraction_No.2_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/0/03/Kyoto-0914_Gel_Extraction_No.2_after.jpg">
 <h4>Ligation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 1,185: / Line 1,224: @@
 <h4>PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Target</th><th>E+X+RBS+mamB+S</th></tr>
 <tr><td>2×KAPA HiFi Hotstart Ready Mix/(&micro;l)</td><td>12.5</td></tr>
-<tr><td>Fw Primer/(&micro;l)</td><td>0.75(E+X+RBS+mamB)</td>/tr>
+<tr><td>Fw Primer/(&micro;l)</td><td>0.75(E+X+RBS+mamB)</td></tr>
 <tr><td>Rv Primer/(&micro;l)</td><td>0.75(S+mamB)</td></tr>
 <tr><td>9/9 DNA Purification Product/(&micro;l)</td><td>Trace</td></tr>
@@ Line 1,207: / Line 1,246: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 1,220: / Line 1,259: @@
 <h3>9/15</h3>
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th></tr>
@@ Line 1,232: / Line 1,271: @@
 <tr><td>9/14 Transformation mamB+pSB1C3 Colony_8</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/1/11/Kyoto-0915_Colony_PCR_No.1.jpg">
+<img src="https://static.igem.org/mediawiki/2014/9/95/Kyoto-0915_Colony_PCR_No.2.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,254: / Line 1,295: @@
 <tr><td>16</td><td>9/14 mamB+pSB1C3 Colony_15</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/a4/Kyoto-0915_Gel_Extraction_No.1_after.jpg">
+<img src="https://static.igem.org/mediawiki/2014/f/fc/Kyoto-0915_Gel_Extraction_No.2_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/5/50/Kyoto-0915_Gel_Extraction_No.2_after.jpg">
 <h4>Colony PCR</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
-<tr><td>9/14 Transformation Pcon+mamL+SB1C3 Colony_1</td></tr>
+<tr><td>9/14 Transformation Pcon+mamL+SBpSB1C3 Colony_1</td></tr>
 <tr><td>9/14 Transformation mamB+pSB1C3 Colony_9</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/8/83/Kyoto-0915_Colony_PCR.jpg">
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 1,272: / Line 1,317: @@
 <h4>Miniprep</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,287: / Line 1,332: @@
 <h4>Liquid Culture</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 1,297: / Line 1,342: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Li</span>
+<p><span class="kyoto-author">Li</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>MilliQ/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,314: / Line 1,359: @@
 <h4>PCR</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Target</th><th>mamB Colony_10</th><th>mamB Colony_11</th></tr>
@@ Line 1,340: / Line 1,385: @@
 <h3>9/16</h3>
 <h4>PCR Labeling and Sequence</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Target</th><th>9/15 Pcon+mamL+pSB1C3</th><th>9/15 mamL+pSB1A2 Colony_1</th><th>9/15 mamL+pSB1A2 Colony_2</th><th>9/15 mamL+pSB1A2 Colony_3</th><th>9/15 mamL+pSB1A2 Colony_4</th><th>9/15 mamB+pSB1C3 Colony_9</th><th>9/15 mamB+pSB1C3 Colony_10</th><th>9/15 mamB+pSB1C3 Colony_11</th></tr>
@@ Line 1,372: / Line 1,417: @@
 <h4>Gel Extraction</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Lane</th><th>Restriction Enzyme Digestion ProductⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,387: / Line 1,432: @@
 <tr><td>11</td><td>9/15 mamL Colony_3(X+P)</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/a3/Kyoto-0916_Gel_Extraction%28Honda%29_No.1_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/6/6a/Kyoto-0916_Gel_Extraction%28Honda%29_No.1_after.jpg">
 <table>
@@ Line 1,397: / Line 1,444: @@
 <tr><td>6</td><td>9/15 mamQ(Nega)</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/b/bf/Kyoto-0916_Gel_Extraction%28Honda%29_No.2_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/d/d0/Kyoto-0916_Gel_Extraction%28Honda%29_No.2_after.jpg">
 <table>
@@ Line 1,407: / Line 1,456: @@
 <h4>Dephosphorylation</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th></tr>
@@ Line 1,415: / Line 1,464: @@
 <h4>DNA Purification</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,423: / Line 1,472: @@
 <h4>Gel Extraction</h4>
-<span class="author">Yamauchi</span>
+<p><span class="kyoto-author">Yamauchi</span></p>
 <table>
 <tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,438: / Line 1,487: @@
 <tr><td>11</td><td>-</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/3/3b/Kyoto-0916_Gel_Extraction%28Yamauchi%29_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/c/cf/Kyoto-0916_Gel_Extraction%28Yamauchi%29_after.jpg">
 <h4>Transformation</h4>
-<span class="author">Honda and Tatsui</span>
+<p><span class="kyoto-author">Honda and Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 1,448: / Line 1,499: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>MilliQ/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,458: / Line 1,509: @@
 <h4>PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Target</th><th>E+Pcon+X+RBS+mamB+His+S(*2)</th></tr>
@@ Line 1,470: / Line 1,521: @@
 <h4>Miniprep</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,484: / Line 1,535: @@
 <h3>9/17</h3>
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 1,498: / Line 1,549: @@
 <h4>Miniprep</h4>
-<span class="author">Tatsui and Yamauchi</span>
+<p><span class="kyoto-author">Tatsui and Yamauchi</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,505: / Line 1,556: @@
 <h4>Gel Extraction</h4>
-<span class="author">Yamauchi</span>
+<p><span class="kyoto-author">Yamauchi</span></p>
 <table>
 <tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,527: / Line 1,578: @@
 <tr><td>Pcon+mamL(S+P)</td><td>285 Error</td><td>1.14</td><td>0.85</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/b/b6/Kyoto-0917_Gel_Extraction_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/8/84/Kyoto-0917_Gel_Extraction_after.jpg">
 <h4>Ligation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 1,536: / Line 1,589: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 1,543: / Line 1,596: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,553: / Line 1,606: @@
 <h4>Liquid Culture</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 1,569: / Line 1,622: @@
 <h3>9/18</h3>
 <h4>Miniprep</h4>
-<span class="author">Tatsui and Honda</span>
+<p><span class="kyoto-author">Tatsui and Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,581: / Line 1,634: @@
 <h4>PCR Labeling and Sequence</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Target</th><th>9/18 Miniprep Mutation mamB Colony_10_3</th><th>9/18 Miniprep Mutation mamB Colony_10_4</th><th>9/18 Miniprep Mutation mamB Colony_11_3</th><th>9/18 Miniprep Mutation mamB Colony_11_4</th><th>9/18 Miniprep Mutation mamB Colony_10_3</th><th>9/18 Miniprep Mutation mamB Colony_10_4</th><th>9/18 Miniprep Mutation mamB Colony_11_3</th><th>9/18 Miniprep Mutation mamB Colony_11_4</th></tr>
@@ Line 1,613: / Line 1,666: @@
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th></tr>
@@ Line 1,625: / Line 1,678: @@
 <tr><td>9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_8</td><td>9/17 Transformation Pcon+mamL+mamQ+pSB1C3 Colony_16</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/d/dc/Kyoto-0918_Colony_PCR.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,650: / Line 1,704: @@
 <h4>DNA Purification</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,657: / Line 1,711: @@
 <h4>Gel Extraction</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,667: / Line 1,721: @@
 <tr><td>6</td><td>-</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/4/4e/Kyoto-0918_Gel_Extraction_No.1_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/8/8d/Kyoto-0918_Gel_Extraction_No.1_after.jpg">
 <table>
@@ Line 1,677: / Line 1,733: @@
 <tr><td>6</td><td>-</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/b/b9/Kyoto-0918_Gel_Extraction_No.2_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/c/c1/Kyoto-0918_Gel_Extraction_No.2_after.jpg">
 <table>
@@ Line 1,684: / Line 1,742: @@
 <h4>Ligation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>10*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 1,692: / Line 1,750: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 1,700: / Line 1,758: @@
 <h4>Liquid Culture</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 1,708: / Line 1,766: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,732: / Line 1,790: @@
 <h3>9/19</h3>
 <h4>Miniprep</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,740: / Line 1,798: @@
 <h4>PCR Labeling and Sequence</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th>Target</th><th>9/19 Miniprep Pcon+mamL+mamQ+pSB1C3</th><th>9/19 Miniprep Pcon+mamL+mamQ+pSB1C3</th><th>9/19 Miniprep Pcon+mamL+mamQ+pSB1C3</th><th>9/19 Miniprep Pcon+mamL+mamQ+pSB1C3</th></tr>
@@ Line 1,762: / Line 1,820: @@
 <h4>Gel Extraction</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,777: / Line 1,835: @@
 <tr><td>11</td><td>9/18 Digestion Mutation mamB Colony_10_4(X+P)</td><td>40</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/c/c3/Kyoto-0919_Gel_Extraction_No.1_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/e/e7/Kyoto-0919_Gel_Extraction_No.1_after.jpg">
 <table>
@@ Line 1,787: / Line 1,847: @@
 <tr><td>6</td><td>-</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/c/cc/Kyoto-0919_Gel_Extraction_No.2_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/1/16/Kyoto-0919_Gel_Extraction_No.2_after.jpg">
 <table>
@@ Line 1,794: / Line 1,856: @@
 <tr><td>3</td><td>9/18 Digestion Pcon+pSB1C3(S+P)</td><td>80</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/d/d0/Kyoto-0919_Gel_Extraction_No.3_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/4/49/Kyoto-0919_Gel_Extraction_No.3_after.jpg">
 <table>
@@ Line 1,804: / Line 1,868: @@
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 1,813: / Line 1,877: @@
 <tr><td>9/18 Transformation Pcon+mamQ+pSB1C3 Colony_5</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/a9/Kyoto-0919_Colony_PCR.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,829: / Line 1,894: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,838: / Line 1,903: @@
 <h4>PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Target</th><th>Pcon+mamB+His</th></tr>
@@ Line 1,863: / Line 1,928: @@
 <h4>DNA Purification</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,871: / Line 1,936: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,878: / Line 1,943: @@
 <h4>Liquid Culture</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Name</th><th>medium</th></tr>
@@ Line 1,889: / Line 1,954: @@
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 1,904: / Line 1,969: @@
 <h3>9/20</h3>
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,917: / Line 1,982: @@
 <h4>Miniprep</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 1,925: / Line 1,990: @@
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th></tr>
@@ Line 1,931: / Line 1,996: @@
 <tr><td>Pcon+mamB+His+pSB3T5 Colony_1(seq_4+VR)</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/7/78/Kyoto-0920_Colony_PCR.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Yasuda</span>
+<p><span class="kyoto-author">Yasuda</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td></tr>
@@ Line 1,945: / Line 2,011: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffur/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 1,955: / Line 2,021: @@
 <h4>Gel Extraction</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
@@ Line 1,978: / Line 2,044: @@
 <tr><td>4</td><td>9/19 Digestion pSB3T5(E+S)</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/a/ac/Kyoto-0920_Gel_Extraction_No.1_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/3/31/Kyoto-0920_Gel_Extraction_No.1_after.jpg">
 <table>
@@ Line 1,986: / Line 2,054: @@
 <tr><td>4</td><td>Digestion Mutation mamB Colony_11_4(Nega)</td><td>-</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/f/f3/Kyoto-0920_Gel_Extraction_No.2_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/4/4b/Kyoto-0920_Gel_Extraction_No.2_after.jpg">
 <table>
@@ Line 1,996: / Line 2,066: @@
 <h4>DNA Purification</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 2,003: / Line 2,073: @@
 <h4>Ligation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>2*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 2,014: / Line 2,084: @@
 <h4>Transformation</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
@@ Line 2,029: / Line 2,099: @@
 <h3>9/22</h3>
 <h4>Colony PCR</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th><th>NameⅢ</th><th>NameⅣ</th></tr>
@@ Line 2,052: / Line 2,122: @@
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td><th>Colony PCR ProductsⅡ</td></tr>
@@ Line 2,075: / Line 2,145: @@
 <h4>Ligation</h4>
-<span class="author">No Name</span>
+<p><span class="kyoto-author">No Name</span></p>
 <table>
 <tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>T4 Ligase/(&micro;l)</th><th>10*Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
@@ Line 2,082: / Line 2,152: @@
 <h4>Restriction Enzyme Digestion</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffur/(&micro;l)</th><th>CLAP/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
@@ Line 2,089: / Line 2,159: @@
 <h4>Colony PCR</h4>
-<span class="author">Honda</span>
+<p><span class="kyoto-author">Honda</span></p>
 <table>
 <tr><th>NameⅠ</th><th>NameⅡ</th><th>NameⅢ</th><th>NameⅣ</th></tr>
@@ Line 2,109: / Line 2,179: @@
 <tr><td>9/20 Transformation Pcon+mamL+mamQ+mamB Colony_11_3_2(Q_F+B_R)</td></tr>
 </table>
+<img src="https://static.igem.org/mediawiki/2014/f/fa/Kyoto-0922_Colony_PCR.jpg">
 <h4>Electrophoresis</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>Lane</th><th>Colony PCR ProductsⅠ</td><th>Colony PCR ProductsⅡ</td><th>Colony PCR ProductsⅢ</td></tr>
@@ Line 2,134: / Line 2,205: @@
 <h4>Miniprep</h4>
-<span class="author">Tatsui</span>
+<p><span class="kyoto-author">Tatsui</span></p>
 <table>
 <tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
@@ Line 2,141: / Line 2,212: @@
 </table>
 </div>
+<div>
+<a name="0927" class="kyoto-jump"></a>
+<h3>9/27</h3>
+<h4>Western Blotting</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<p>Make the 20% acrilamid gel apray the following</p>
+<table>
+<tr><th>Lane</th><th>Sample</th></tr>
+<tr><td>1-5 9-12</td><td>Sample buffer</td></tr>
+<tr><td>6</td><td>T7-RBS-pSB1C3(control)</td></tr>
+<tr><td>7</td><td>pL(pSB1C3)</td></tr>
+<tr><td>8</td><td>protein marker</td></tr>
+</table>
+<p>Electrophoresis:200V 25mA 30min</p>
+<p>Transcription:50V 200mA 73min</p>
+<h4>Liquid Culture</h4>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>pLQB(9/22 master)</td></tr>
+<tr><td>pLQ(9/22 master)</td></tr>
+</table>
+</div>
+<div>
+<a name="0928" class="kyoto-jump"></a>
+<h3>9/28</h3>
+<h4>Fixation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>25% Glyceraldehyde/(ml)</th><th>Phosphate buffer/(ml)</th><th>MilliQ/(ml)</th><th>Total/(ml)</th></tr>
+<tr><td>1.25</td><td>5.0</td><td>3.75</td><td>10.0</td></tr>
+</table>
+</div>
+<div>
+<a name="0929" class="kyoto-jump"></a>
+<h3>9/29</h3>
+<h4>Liquid Culture</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>9/22 master pLQB</td></tr>
+<tr><td>9/22 master pLQ</td></tr>
+<tr><td>9/22 master pL</td></tr>
+<tr><td>9/22 master pQ-3</td></tr>
+<tr><td>9/22 master pQ-5</td></tr>
+<tr><td>9/20 master pB-22</td></tr>
+<tr><td>9/20 master pB-23</td></tr>
+</table>
+<h4>Fixation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Osmic acid/(ml)</th><th>Phosphate buffer/(ml)</th><th>Total/(ml)</th></tr>
+<tr><td>4</td><td>4</td><td>8</td></tr>
+</table>
+</div>
+<div>
+<a name="0930" class="kyoto-jump"></a>
+<h3>9/30</h3>
+<h4>Miniprep</h4>
+<p><span class="kyoto-author">Tatsui</span></p>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>9/29 Liquid Culture pLQB</td><td>-</td><td>-</td><td>-</td></tr>
+<tr><td>9/29 Liquid Culture pLQ</td><td>-</td><td>-</td><td>-</td></tr>
+</table>
+<h4>Western Blotting</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<p>Make the 20% acrilamid gel apray the following</p>
+<table>
+<tr><th>Lane</th><th>Sample</th></tr>
+<tr><td>2</td><td>Marker</td></tr>
+<tr><td>3</td><td>pLQB</td></tr>
+<tr><td>4</td><td>pLQ</td></tr>
+<tr><td>5</td><td>pL</td></tr>
+<tr><td>6</td><td>pQ-3</td></tr>
+<tr><td>7</td><td>pQ-5</td></tr>
+<tr><td>8</td><td>pB</td></tr>
+<tr><td>9</td><td>GTP-His</td></tr>
+<tr><td>10</td><td>T7-RBS-pSB1C3(control)</td></tr>
+<tr><td>11</td><td>Sample buffer</td></tr>
+</table>
+<p>Electrophoresis:200V 25mA 1h30min</p>
+<p>Transcription:50V 200mA 73min</p>
+<h4>Liquid Culture</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>9/22 master pLQB</td></tr>
+<tr><td>9/22 master pQ(3)</td></tr>
+</table>
+</div>
+<div>
+<a name="1001" class="kyoto-jump"></a>
+<h3>10/1</h3>
+<h4>Ethanol Precipitation</h4>
+<p><span class="kyoto-author">Tatsui</span></p>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>9/28 pL(pSB1C3)(VF)(Miniprep product)</td></tr>
+<tr><td>9/28 pL(pSB1C3)(VR)(Miniprep product)</td></tr>
+<tr><td>9/22 pB(22)(VF)(Miniprep product)</td></tr>
+<tr><td>9/22 pB(22)(VR)(Miniprep product)</td></tr>
+<tr><td>9/22 pB(23)(VF)</td></tr>
+<tr><td>9/22 pB(23)(VR)</td></tr>
+<tr><td>10/1 pQ(3)(VF)(Miniprep product)</td></tr>
+<tr><td>10/1 pQ(3)(VR)(Miniprep product)</td></tr>
+<tr><td>10/1 pLQB(VF)(Miniprep product)</td></tr>
+<tr><td>10/1 pLQB(seq-1)(Miniprep product)</td></tr>
+<tr><td>10/1 pLQB(seq-2)(Miniprep product)</td></tr>
+<tr><td>10/1 pLQB(seq-3)(Miniprep product)</td></tr>
+<tr><td>10/1 pLQB(seq-4)(Miniprep product)</td></tr>
+<tr><td>10/1 pLQB(VR)(Miniprep product)</td></tr>
+</table>
+<h4>Liquid Culture</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>9/22 master Plate pLQB</td></tr>
+<tr><td>9/22 master Plate pQ(3)</td></tr>
+</table>
+<h4>Restriction Enzyme Digestion</h4>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
+<tr><td>9/23 pQ</td><td>30</td><td>3</td><td>0</td><td>3</td><td>1</td><td>9</td><td>44</td><td>90</td></tr>
+<tr><td>pQ(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>8</td><td>10</td></tr>
+<tr><td>9/2 Pcon(pSB1C3)</td><td>30</td><td>0</td><td>3</td><td>3</td><td>1</td><td>9</td><td>44</td><td>90</td></tr>
+<tr><td>9/2 Pcon(pSB1C3)(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>8</td><td>10</td></tr>
+</table>
+<h4>Miniprep</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>9/29 Liquid Culture pLQB</td><td>-</td><td>-</td><td>-</td></tr>
+<tr><td>9/29 Liquid Culture pQ(3)</td><td>-</td><td>-</td><td>-</td></tr>
+<tr><td>9/29 Liquid Culture pQ(22)</td><td>-</td><td>-</td><td>-</td></tr>
+<tr><td>9/29 Liquid Culture pQ(23)</td><td>-</td><td>-</td><td>-</td></tr>
+</table>
+<h4>Sequence PCR</h4>
+<table>
+<tr><th>Target</th><th>9/28 pL(pSB1C3)(VF)(Miniprep product)</th><th>9/28 pL(pSB1C3)(VR)(Miniprep product)</th><th>9/22 pB(22)(VF)(Miniprep product)</th><th>9/22 M pB(22)(VR)</th><th>9/22 pB(23)(VF)</th><th>9/22 pB(23)(VR)</th><th>10/1 M pQ(3)(VF)</th><th>10/1 M pQ(3)(VR)</th><th>10/1 M pLQB(VF)</th><th>10/1 M pLQB(seq-1)</th><th>10/1 M pLQB(seq-2)</th><th>10/1 M pLQB(seq-3)</th><th>10/1 M pLQB(seq-4)</th><th>10/1 M pLQB(VR)</th></tr>
+<tr><td>Template/(&micro;l)</td><td>4.7</td><td>4.7</td><td>1.6</td><td>1.6</td><td>3.2</td><td>3.2</td><td>5</td><td>5</td><td>5</td><td>5</td><td>5</td><td>5</td><td>5</td><td>5</td></tr>
+<tr><td>Big dye/(&micro;l)</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td></tr>
+<tr><td>5×Buffer/(&micro;l)</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td></tr>
+<tr><td>Primer(VF)/(&micro;l)</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td></tr>
+<tr><td>MilliQ/(&micro;l)</td><td>3.05</td><td>3.05</td><td>6.15</td><td>6.15</td><td>4.55</td><td>4.55</td><td>2.75</td><td>2.75</td><td>2.75</td><td>2.75</td><td>2.75</td><td>2.75</td><td>2.75</td><td>2.75</td></tr>
+<tr><td>TOTAL/(&micro;l)</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td></tr>
+</table>
+<table>
+<tr><th>Steps</th><th>Temparature</th><th>Time</th><th>cycle</th></tr>
+<tr><td>Pre Denature</td><td>96℃</td><td>2min</td><td>1time</td></tr>
+<tr><td>Denature</td><td>96℃</td><td>10sec</td><td>30cycle</td></tr>
+<tr><td>Annealing</td><td>55℃</td><td>5sec</td><td>30cycle</td></tr>
+<tr><td>Extension</td><td>60℃</td><td>4min</td><td>30cycle</td></tr>
+<tr><td>Final elongation</td><td>4℃</td><td>1min</td><td>1time</td></tr>
+<tr><td>Final hold</td><td>4℃</td><td>infinity</td><td>-</td></tr>
+</table>
+<h4>Gel Extraction</h4>
+<p>(1)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>1</td><td>blank</td><td>-</td></tr>
+<tr><td>2</td><td>1400b ladder</td><td>-</td></tr>
+<tr><td>3</td><td>His-OE-1</td><td>-</td></tr>
+<tr><td>4</td><td>1kb ladder</td><td>-</td></tr>
+<tr><td>5</td><td>750b ladder</td><td>-</td></tr>
+<tr><td>6</td><td>His-OE-2</td><td>-</td></tr>
+</table>
+<p>(2)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅡ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>3,6</td><td>pQ(X,P)</td><td>-</td></tr>
+<tr><td>4</td><td>100b ladder</td><td>-</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/e/e4/Kyoto-1001_Gel_Extraction_No.2.jpg">
+<p>(3)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅢ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>3,6</td><td>Pcon pSB1C3(S,P)</td><td>-</td></tr>
+<tr><td>4</td><td>1kb ladder</td><td>-</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/d/dc/Kyoto-1001_Gel_Extraction_No.3_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/9/99/Kyoto-1001_Gel_Extraction_No.3_after.jpg">
+<p>(4)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅣ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>3</td><td>DiDECARB-4</td><td>-</td></tr>
+<tr><td>6</td><td>DiDECARB-5</td><td>-</td></tr>
+<tr><td>2</td><td>DiDECARB-4(control)</td><td>-</td></tr>
+<tr><td>5</td><td>DiDECARB-5(control)</td><td>-</td></tr>
+<tr><td>4</td><td>1kb ladder</td><td>-</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/5/55/Kyoto-1001_Gel_Extraction_No.4_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/d/d1/Kyoto-1001_Gel_Extraction_No.4_after.jpg">
+</div>
+<div>
+<a name="1002" class="kyoto-jump"></a>
+<h3>10/2</h3>
+<h4>Miniprep</h4>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>pLQB</td><td>390</td><td>1.70</td><td>1.20</td></tr>
+<tr><td>pLQ</td><td>319</td><td>1.64</td><td>0.92</td></tr>
+<tr><td>j04450</td><td>255</td><td>1.59</td><td>1.04</td></tr>
+</table>
+</div>
+<div>
+<a name="1003" class="kyoto-jump"></a>
+<h3>10/3</h3>
+<h4>PCR</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Target</th><th>Volume</th></tr>
+<tr><td>10×buffur for KOD Plus Ver.2/(&micro;l)</td><td>5</td></tr>
+<tr><td>2mMdNTPs/(&micro;l)</th><td>5</td></tr>
+<tr><td>25mM MgSO4/(&micro;l)</td><td>3</td></tr>
+<tr><td>VF Primer/(&micro;l)</td><td>1.5</td></tr>
+<tr><td>VR Primer/(&micro;l)</td><td>1.5</td></tr>
+<tr><td>template/(&micro;l)</td><td>1</td></tr>
+<tr><td>KOD-plus/(&micro;l)</td><td>1</td></tr>
+<tr><td>MilliQ/(&micro;l)</td><td>33</td></tr>
+<tr><td>TOTAL/(&micro;l)</td><td>50</td></tr>
+</table>
+<h4>DNA Purification</h4>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>10/3 PB</td><td>39.8</td><td>1.75</td><td>0.92</td></tr>
+</table>
+<h4>Digestion</h4>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoRI/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>BSA</th><th>Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
+<tr><td>10/3 Column pB</td><td>15.8</td><td>1</td><td>1</td><td>0.2</td><td>2</td><td>-</td><td>20</td></tr>
+</table>
+<h4>Restriction Enzyme Digestion</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
+<tr><td>DiDECARB-4</td><td>10</td><td>2</td><td>2</td><td>0.4</td><td>4</td><td>21.6</td><td>40</td></tr>
+<tr><td>DiDECARB-4(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>8</td><td>10</td></tr>
+<tr><td>DiDECARB-5</td><td>10</td><td>2</td><td>2</td><td>0.4</td><td>4</td><td>21.6</td><td>40</td></tr>
+<tr><td>DiDECARB-5(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>8</td><td>10</td></tr>
+</table>
+<h4>Gel Extraction</h4>
+<p><span class="kyoto-author">Tatsui</span></p>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>pSB1C3(X,P)-4</td><td>942</td><td>1.89</td><td>1.26</td></tr>
+<tr><td>pSB1C3(X,P)-5</td><td>518</td><td>1.87</td><td>1.26</td></tr>
+</table>
+<div>
+<div>
+<a name="1004" class="kyoto-jump"></a>
+<h3>10/4</h3>
+<h4>Digestion</h4>
+<p><span class="kyoto-author">Tatsui</span></p>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>BSA</th><th>Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
+<tr><td>9/18 MP pL-pSB1C3(85)</td><td>24</td><td>1</td><td>1</td><td>0.4</td><td>4</td><td>9.6</td><td>40</td></tr>
+<tr><td>9/18 MP pL-pSB1C3(85)(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>8</td><td>10</td></tr>
+<tr><td>9/18 MP B&micro;-pSB1C3-11-3(355)</td><td>6</td><td>1</td><td>1</td><td>0.4</td><td>4</td><td>27.6</td><td>40</td></tr>
+<tr><td>9/18 MP B&micro;-pSB1C3-11-3(355)(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>1</td><td>8</td><td>10</td></tr>
+</table>
+<h4>Gel Extraction</h4>
+<p>(1)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>1</td><td>10/4 B&micro; pSB1C3-11-3(control)</td><td>-</td></tr>
+<tr><td>3,4</td><td>10/4 B&micro; pSB1C3-11-3(XP)</td><td>-</td></tr>
+<tr><td>6</td><td>ladder</td><td>-</td></tr>
+</table>
+<p>(2)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅡ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>1</td><td>ladder</td><td>-</td></tr>
+<tr><td>3,4</td><td>10/4 pL-pSB1C3(XP)</td><td>-</td></tr>
+<tr><td>6</td><td>10/4 pL-pSB1C3(control)</td><td>-</td></tr>
+</table>
+<h4>Ligation</h4>
+<p><span class="kyoto-author">No name</span></p>
+<table>
+<tr><th>Sample</th><th>Vector/(&micro;L)</th><th>Insert/(&micro;L)</th><th>Ligase/(&micro;l)</th><th>Buffer/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
+<tr><td>9/20 Q-pSB1C3(B)</td><td>1</td><td>3</td><td>1</td><td>5</td><td>0</td><td>10</td></tr>
+<tr><td>9/16 Q-pSB1C3(B)</td><td>1</td><td>3</td><td>1</td><td>5</td><td>0</td><td>10</td></tr>
+<tr><td>9/20 Q-pSB1C3(B)(control)</td><td>1</td><td>0</td><td>1</td><td>5</td><td>3</td><td>10</td></tr>
+<tr><td>9/16Q-pSB1C3(B)(control)</td><td>1</td><td>0</td><td>1</td><td>5</td><td>3</td><td>10</td></tr>
+</table>
+<h4>Transformation</h4>
+<table>
+<tr><th>Sample</th><th>Plasmid/(&micro;l)</th><th>CompetentCells(DH5&alpha;)/(&micro;l)</th></tr>
+<tr><td>E1</td><td>2</td><td>10</td></tr>
+<tr><td>E2</td><td>2</td><td>10</td></tr>
+<tr><td>E3</td><td>2</td><td>10</td></tr>
+<tr><td>E4</td><td>2</td><td>10</td></tr>
+</table>
+</div>
+<div>
+<a name="1005" class="kyoto-jump"></a>
+<h3>10/5</h3>
+<h4>Ethanol Precipitation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<p>10/3 Gel Extraction PconpSB1C3(SP)</p>
+<h4>Ligation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>sample</th><th>Vector/(&micro;L)</th><th>Insert/(&micro;L)</th><th>Toyobo Ligation high/(&micro;l)</th></tr>
+<tr><td>10/5 PconpSB1C3(SP)+9/20pQ(3)(XP)</td><td>1</td><td>1</td><td>2</td></tr>
+<tr><td>10/5 PconpSB1C3(SP)(control)</td><td>1</td><td>1</td><td>2</td></tr>
+</table>
+<h4>Transformation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th><th>Plasmid/(&micro;l)</th><th>CompetentCells(DH5&alpha;)/(&micro;l)</th></tr>
+<tr><td>F1</td><td>2</td><td>10</td></tr>
+<tr><td>F2</td><td>2</td><td>10</td></tr>
+</table>
+<h4>Colony PCR</h4>
+<table>
+<tr><th>Lane</th><th>Colony PCR ProductsⅠ</th></tr>
+<tr><td>9-14</td><td>E1 1-6</td></th>
+<tr><td>15-20</td><td>E2 1-6</td></th>
+</table>
+<h4>Liquid Culture</h4>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>E1 1-6</td></tr>
+<tr><td>E2 1-6</td></tr>
+</table>
+<h4>DNA Purification</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>pB PCR</td><td>57</td><td>2.06</td><td>2.39</td></tr>
+</table>
+<h4>Digestion</h4>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoRI/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffer/(&micro;l)</th><th>BSA</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
+<tr><td>9/18 MP B&micro;(pSB1C3)11-4(ES)</td><td>10</td><td>1</td><td>0</td><td>1</td><td>0</td><td>4</td><td>0.4</td><td>23.6</td><td>40</td></tr>
+<tr><td>9/18 MP B&micro;(pSB1C3)11-4(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>8</td><td>10</td></tr>
+<tr><td>9/22 MP pQ-3(XP)</td><td>40</td><td>0</td><td>4</td><td>0</td><td>4</td><td>16</td><td>1.6</td><td>94.4</td><td>160</td></tr>
+<tr><td>9/22 MP pQ-3(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>8</td><td>10</td></tr>
+<tr><td>9/22 Pcon Master(SP)</td><td>10</td><td>0</td><td>0</td><td>1</td><td>1</td><td>4</td><td>0.4</td><td>23.6</td><td>40</td></tr>
+<tr><td>9/22 Pcon Master(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1</td><td>0</td><td>8</td><td>10</td></tr>
+<tr><td>9/22 pB(PCR Product)(ES)</td><td>20</td><td>1</td><td>0</td><td>1</td><td>0</td><td>4</td><td>0.4</td><td>13.6</td><td>40</td></tr>
+<tr><td>9/22 pB(PCR Product)(control)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>10/td><td>1</td><td>0</td><td>8</td><td>10</td></tr>
+</table>
+<h4>PCR</h4>
+<p><span class="kyoto-author">No Name</span></p>
+<table>
+<tr><th>Target</th><th>Volume</th></tr>
+<tr><td>2×KAPA HiFi Hotstart Ready Mix/(&micro;l)</td><td>12.5</td></tr>
+<tr><td>Fw Primer/(&micro;l)</td><td>0.75</td></tr>
+<tr><td>Rv Primer/(&micro;l)</td><td>0.75</td></tr>
+<tr><td>Template(9/22 Mini Pcon-mamQ-3)</td><td>pick up</td></tr>
+<tr><td>MilliQ/(&micro;l)</td><td>11</td></tr>
+<tr><td>TOTAL/(&micro;l)</td><td>25</td></tr>
+</table>
+<table>
+<tr><th>Steps</th><th>Temparature</th><th>Time</th><th>cycle</th></tr>
+<tr><td>Pre Denature</td><td>98℃</td><td>5min</td><td>1time</td></tr>
+<tr><td>Denature</td><td>98℃</td><td>20sec</td><td>30cycle</td></tr>
+<tr><td>Annealing</td><td>60℃</td><td>15sec</td><td>30cycle</td></tr>
+<tr><td>Extension</td><td>72℃</td><td>30sec</td><td>30cycle</td></tr>
+<tr><td>Final elongation</td><td>72℃</td><td>5min</td><td>1time</td></tr>
+<tr><td>Final hold</td><td>12℃</td><td>-</td><td>-</td></tr>
+</table>
+</div>
+<div>
+<a name="1006" class="kyoto-jump"></a>
+<h3>10/6</h3>
+<h4>Sequence PCR</h4>
+<table>
+<tr><th>Target</th><th>10/6 T7-RBS-his(pSB1C3)-1-VF(Miniprep product)</th><th>10/6 T7-RBS-his(pSB1C3)-1-VR(Miniprep product)</th><th>10/6 T7-RBS-his(pSB1C3)-2-VF(Miniprep product)</th><th>10/6 T7-RBS-his(pSB1C3)-2-VR(Miniprep product)</th><th>10/6 T7-RBS-his(pSB1C3)-3-VF(Miniprep product)</th><th>10/6 T7-RBS-his(pSB1C3)-3-VR(Miniprep product)</th><th>10/6 Q(pSB1C3)E1-1 VF(Miniprep product)</th><th>10/6 Q(pSB1C3)E1-1 VR(Miniprep product)</th><th>10/6 M Q(pSB1C3)E1-2-VF</th><th>10/6 Q(pSB1C3)E1-2-VR(Miniprep product)</th><th>10/6 M Q(pSB1C3)E1-3-VF</th><th>10/6 M Q(pSB1C3)E1-3-VR</th><th>10/6 M Q(pSB1C3)E2-1-VF</th><th>10/6 M Q(pSB1C3)E2-1-VR</th><th>10/6 Q(pSB1C3)E2-2-VF(Miniprep product)</th><th>10/6 Q(pSB1C3)E2-2-VR(Miniprep product)</th></tr>
+<tr><td>Template/(&micro;l)</td><td>2.2</td><td>2.2</td><td>2.5</td><td>2.5</td><td>2.5</td><td>2.5</td><td>1.85</td><td>1.85</td><td>1.1</td><td>1.1</td><td>1.7</td><td>1.7</td><td>1.8</td><td>1.8</td><td>1.7</td><td>1.7</td></tr>
+<tr><td>Big dye/(&micro;l)</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td></tr>
+<tr><td>5×Buffer/(&micro;l)</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td><td>1.75</td></tr>
+<tr><td>Primer/(&micro;l)</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td><td>0.5</td></tr>
+<tr><td>MilliQ/(&micro;l)</td><td>5.55</td><td>5.55</td><td>5.25</td><td>5.25</td><td>5.25</td><td>5.25</td><td>5.9</td><td>5.9</td><td>6.65</td><td>6.65</td><td>6.05</td><td>6.05</td><td>5.95</td><td>5.95</td><td>6.05</td><td>6.05</td></tr>
+<tr><td>TOTAL/(&micro;l)</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td><td>10.5</td></tr>
+</table>
+<table>
+<tr><th>Steps</th><th>Temparature</th><th>Time</th><th>cycle</th></tr>
+<tr><td>Pre Denature</td><td>96℃</td><td>2min</td><td>1time</td></tr>
+<tr><td>Denature</td><td>96℃</td><td>10sec</td><td>30cycle</td></tr>
+<tr><td>Annealing</td><td>50℃</td><td>5sec</td><td>30cycle</td></tr>
+<tr><td>Extension</td><td>60℃</td><td>4min</td><td>30cycle</td></tr>
+<tr><td>Final elongation</td><td>4℃</td><td>1min</td><td>1time</td></tr>
+<tr><td>Final hold</td><td>4℃</td><td>infinity</td><td>-</td></tr>
+</table>
+<h4>Miniprep</h4>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>T7-RBS-his(pSB1C3)-1</td><td>180</td><td>1.84</td><td>1.76</td></tr>
+<tr><td>T7-RBS-his(pSB1C3)-2</td><td>160</td><td>1.92</td><td>1.92</td></tr>
+<tr><td>T7-RBS-his(pSB1C3)-3</td><td>156</td><td>1.69</td><td>1.64</td></tr>
+<tr><td>E1-1</td><td>216</td><td>1.84</td><td>2.04</td></tr>
+<tr><td>E1-2</td><td>355</td><td>1.82</td><td>2.31</td></tr>
+<tr><td>E1-3</td><td>238</td><td>1.81</td><td>2.11</td></tr>
+<tr><td>E2-1</td><td>225</td><td>1.83</td><td>2.00</td></tr>
+<tr><td>E2-2</td><td>230</td><td>1.76</td><td>1.84</td></tr>
+</table>
+<h4>Gel Extraction</h4>
+<p>(1)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>1</td><td>10/5 B&micro(pSB1C3)(control)</td><td>-</td></tr>
+<tr><td>3</td><td>10/5 B&micro(pSB1C3)(ES)</td><td>-</td></tr>
+<tr><td>6</td><td>10/5 pB(ES)</td><td>-</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/5/5e/Kyoto-1006_Gel_Extraction_No.1_before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/d/df/Kyoto-1006_Gel_Extraction_No.1_after.jpg">
+<p>(2)</p>
+<table>
+<tr><th>Lane</th><th>SampleⅡ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>1</td><td>pQ-3(control)</td><td>-</td></tr>
+<tr><td>3</td><td>pQ-3(XP)</td><td>-</td></tr>
+<tr><td>4</td><td>Pcon(control)</td><td>-</td></tr>
+<tr><td>6</td><td>Pcon(SP)</td><td>-</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/6/6b/Kyoto-1006_Gel_Extraction_No.2_after.jpg">
+</div>
+<div>
+<a name="1007" class="kyoto-jump"></a>
+<h3>10/7</h3>
+<h4>Liquid Culture</h4>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>pLQB(9/22)</td></tr>
+<tr><td>pLQ(9/22)</td></tr>
+<tr><td>pL(9/22)</td></tr>
+<tr><td>control(T7-RBS)(9/18)</td></tr>
+</table>
+</div>
+<div>
+<a name="1008" class="kyoto-jump"></a>
+<h3>10/8</h3>
+<h4>Ligation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>sample</th><th>Insert/(&micro;L)</th><th>Vector/(&micro;L)</th><th>2x Ligation high/
+(&micro;l)</th><th>MilliQ</th><th>TOTAL</th></tr>
+<tr><td>pQ pSB1C3</td><td>1</td><td>1</td><td>2</td><td>0</td><td>4</td></tr>
+<tr><td>pQ pSB1C3(control)</td><td>0</td><td>1</td><td>2</td><td>1</td><td>4</td></tr>
+<tr><td>pB pSB1C3</td><td>1</td><td>1</td><td>2</td><td>0</td><td>4</td></tr>
+<tr><td>pB pSB1C3(control)</td><td>0</td><td>1</td><td>2</td><td>1</td><td>4</td></tr>
+</table>
+<h4>Liquid Culture</h4>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>9/22 pLQB</td></tr>
+<tr><td>9/22 pLQ</td></tr>
+<tr><td>9/22 pL</td></tr>
+<tr><td>9/18 control(T7-RBS)(9/18)</td></tr>
+</table>
+<h4>Inoculation</h4>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>10/7 pLQB</td></tr>
+<tr><td>10/7 pLQ</td></tr>
+<tr><td>10/7 pL</td></tr>
+<tr><td>10/7 control</td></tr>
+</table>
+<p>16:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>BL21</td><td>0.224</td></tr>
+<tr><td>LQB</td><td>0.031</td></tr>
+<tr><td>LQ</td><td>0.061</td></tr>
+</table>
+<p>17:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>BL21</td><td>0.720</td></tr>
+<tr><td>LQB</td><td>0.057</td></tr>
+<tr><td>LQ</td><td>0.139</td></tr>
+</table>
+<p>18:00</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQ</td><td>0.088</td></tr>
+<tr><td>LQB</td><td>0.211</td></tr>
+</table>
+<p>18:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQ</td><td>0.267</td></tr>
+<tr><td>LQB</td><td>0.122</td></tr>
+</table>
+<p>19:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.216</td></tr>
+<tr><td>LQ</td><td>0.412</td></tr>
+</table>
+<p>10/9 13:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB(morning)</td><td>1.657</td></tr>
+<tr><td>LQ</td><td>1.625</td></tr>
+<tr><td>LQB(evening)</td><td>1.014</td></tr>
+<tr><td>-</td><td>0.064</td></tr>
+<tr><td>LQ</td><td>1.652</td></tr>
+<tr><td>L</td><td>2.117</td></tr>
+<tr><td>control</td><td>2.124</td></tr>
+</table>
+</div>
+<div>
+<a name="1009" class="kyoto-jump"></a>
+<h3>10/9</h3>
+<h4>Colony PCR</h4>
+<table>
+<tr><th>Target</th><th>Volume</th></tr>
+<tr><td>2x quick tag/(&micro;l)</td><td>15</td></tr>
+<tr><td>VF Primer/(&micro;l)</td><td>0.6</td></tr>
+<tr><td>VR Primer/(&micro;l)</td><td>0.6</td></tr>
+<tr><td>MilliQ/(&micro;l)</td><td>13.8</td></tr>
+<tr><td>TOTAL/(&micro;l)</td><td>30</td></tr>
+</table>
+<table>
+<tr><th>Steps</th><th>Temparature</th><th>Time</th><th>cycle</th></tr>
+<tr><td>Pre Denature</td><td>94℃</td><td>2min</td><td>1time</td></tr>
+<tr><td>Denature</td><td>94℃</td><td>30sec</td><td>30cycle</td></tr>
+<tr><td>Annealing</td><td>55℃</td><td>30sec</td><td>30cycle</td></tr>
+<tr><td>Extension</td><td>68℃</td><td>1min</td><td>30cycle</td></tr>
+<tr><td>Final elongation</td><td>68℃</td><td>7min</td><td>1time</td></tr>
+<tr><td>Final hold</td><td>4℃</td><td>infinity</td><td>-</td></tr>
+</table>
+<h4>Transformation</h4>
+<table>
+<tr><th>Sample</th><th>Plasmid/(&micro;l)</th><th>CompetentCells(DH5&alpha;)/(&micro;l)</th><th>TOTAL/(&micro;l)</th></tr>
+<tr><td>pQ</td><td>2</td><td>20</td><td>22</td></tr>
+<tr><td>pB</td><td>2</td><td>20</td><td>22</td></tr>
+<tr><td>pQ(control)</td><td>2</td><td>20</td><td>22</td></tr>
+<tr><td>pB(control)</td><td>2</td><td>20</td><td>22</td></tr>
+</table>
+<h4>Inoculation</h4>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>10/8 pLQB</td></tr>
+<tr><td>10/8 pLQ</td></tr>
+<tr><td>10/8 pL</td></tr>
+<tr><td>10/8 control</td></tr>
+</table>
+<p>14:00</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.177</td></tr>
+<tr><td>LQ</td><td>0.306</td></tr>
+<tr><td>L</td><td>0.477</td></tr>
+<tr><td>control</td><td>0.435</td></tr>
+</table>
+<p>14:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.240</td></tr>
+<tr><td>LQ</td><td>0.351</td></tr>
+<tr><td>L</td><td>0.641</td></tr>
+<tr><td>control</td><td>0.640</td></tr>
+</table>
+<p>15:00</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.351</td></tr>
+<tr><td>LQ</td><td>0.395</td></tr>
+</table>
+<p>15:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.413</td></tr>
+<tr><td>LQ</td><td>0.397</td></tr>
+</table>
+<p>16:00</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.564</td></tr>
+<tr><td>LQ</td><td>0.458</td></tr>
+</table>
+<p>16:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.732</td></tr>
+<tr><td>LQ</td><td>0.518</td></tr>
+</table>
+<p>17:00</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQ</td><td>0.581</td></tr>
+</table>
+<p>17:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQ</td><td>0.458</td></tr>
+</table>
+<p>18:00</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQ</td><td>0.749</td></tr>
+</table>
+</div>
+<div>
+<a name="1010" class="kyoto-jump"></a>
+<h3>10/10</h3>
+<h4>Electrophoresis</h4>
+<p>Honda</p>
+<table>
+<tr><th>Lane</th><th>PCR Product</th></tr>
+<tr><td>1</td><td>1kb ladder</td></tr>
+<tr><td>2</td><td>10/9 pB(pSB1C3) Colony_1</td></tr>
+<tr><td>3</td><td>10/9 Negative Control</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/0/0f/1010electrophoresis1.jpg">
+<h4>Restriction Enzyme Digestion</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>BSA/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>TOTAL/(&micro;l)</tr>
+<tr><td>9/15 pLQ</td><td>5</td><td>0.5</td><td>0</td><td>0</td><td>0.5</td><td>2(H)</td><td>0.5</td><td>11.5</td><td>20</td></tr>
+<tr><td>10/2 pLQB</td><td>7</td><td>1</td><td>0</td><td>0</td><td>1</td><td>4(H)</td><td>0.5</td><td>26.5</td><td>40</td></tr>
+<tr><td>10/2 pLQB(Nega)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1(H)</td><td>0</td><td>8</td><td>10</td></tr>
+<tr><td>9/2 pSB4A5</td><td>10</td><td>1</td><td>0</td><td>0</td><td>1</td><td>4(H)</td><td>0.5</td><td>26.5</td><td>40</td></tr>
+<tr><td>9/2 pSB4A5(Nega)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1(H)</td><td>0</td><td>8</td><td>10</td></tr>
+</tr>
+</table>
+<p>20:00~ O/N</p>
+<h4>Liquid Culture</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Name</th><th>medium</th></tr>
+<tr><td>10/6 Transformation Pcon+mamB+pSB1C3 Colony_1</td><td>LB medium(CP)*2</td></tr>
+<tr><td>9/22 Master Plate Pcon+mamL+mamQ</td><td>LB medium(CP)*2</td></tr>
+</table>
+<h4>Miniprep</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>10/10 Liquid culture Pcon+mamB colony_1 </td><td>74</td><td>1.70</td><td>3.82</td></tr>
+<tr><td>10/10 Liquid culture Pcon+mamL+mamQ </td><td>59</td><td>1.88</td><td>5.10</td></tr>
+</table>
+<h4>Gel Extraction</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Lane</th><th>SampleⅠ</th><th>Volume/(&micro;l)</th></tr>
+<tr><td>2</td><td>10/10 Pcon+mamL+mamQ+mamB (Nega)</td><td>5</td></tr>
+<tr><td>4</td><td>10/10 Pcon+mamL+mamQ+mamB (E+P)</td><td>35</td></tr>
+<tr><td>7</td><td>10/10 Pcon+mamL+mamQ (E+P)</td><td>20</td></tr>
+<tr><td>10</td><td>10/10 pSB4A5 (Nega)</td><td>5</td></tr>
+<tr><td>12</td><td>10/10 pSB4A5 (E+P)</td><td>35</td></tr>
+<tr><td>14</td><td>1kb ladder </td><td>3</td></tr>
+</table>
+<img src="https://static.igem.org/mediawiki/2014/8/84/1011gelextraction1before.jpg">
+<img src="https://static.igem.org/mediawiki/2014/0/0c/1011gelextraction1after.jpg">
+<div>
+<a name="1013" class="kyoto-jump"></a>
+<h3>10/13</h3>
+<h4>Restriction Enzyme Digestion</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Sample</th><th>DNA/(&micro;l)</th><th>EcoR1/(&micro;l)</th><th>Xba1/(&micro;l)</th><th>Spe1/(&micro;l)</th><th>Pst1/(&micro;l)</th><th>Buffur/(&micro;l)</th><th>BSA/(&micro;l)</th><th>MilliQ/(&micro;l)</th><th>CIAP/(&micro;l)</tr><th>TOTAL/(&micro;l)</tr>
+<tr><td>10/11 Miniprep Pcon+mamL+mamQ</td><td>23</td><td>1</td><td>0</td><td>0</td><td>1</td><td>4(H)</td><td>0.5</td><td>11.5</td><td>1</td><td>41</td></tr>
+<tr><td>10/11 Miniprep Pcon+mamL+mamQ(Nega)</td><td>1</td><td>0</td><td>0</td><td>0</td><td>0</td><td>1(H)</td><td>0</td><td>8</td><td>0</td><td>10</td></tr>
+</tr>
+</table>
+<p>11:00~ 2hours</p>
+<h4>DNA Purification</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>DNA</th><th>Concentration/(&micro;g/ml)</th><th>260/280</th><th>260/230</th></tr>
+<tr><td>10/13 Digestion Pcon+mamL+mamQ(E+P)</td><td>59</td><td>1.79</td><td>-0.66</td></tr>
+</table>
+<h4>Ligation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th colspan=2>Insert/(&micro;L)</th><th colspan=2>Vector/(&micro;L)</th><th>2*Ligation high/(&micro;l)</th><th>Total/(&micro;l)</th></tr>
+<tr><td>10/13 Pcon+mamL+mamQ (E+P)</td><td>2</td><td>10/11 pSB4A5 (E+P)(2 fold dilution)</td><td>2</td><td>4</td><td>8</td></tr>
+<tr><td>10/11 Pcon+mamL+mamQ+mamB(E+P)</td><td>2</td><td>10/11 pSB4A5 (E+P)(2 fold dilution)</td><td>2</td><td>4</td><td>8</td></tr>
+</table>
+<h4>Transformation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th colspan=2>Sample/(&micro;L)</th><th>CompetentCells/(&micro;l)</th><th>Total/(&micro;l)</th><th>Medium</th></tr>
+<tr><td>10/10 Ligation Pcon+mamL+mamQ+pSB4A5</td><td>6</td><td>30(2/23)</td><td>36</td><td>LB(CP)</td></tr>
+<tr><td>10/10 Ligation Pcon+mamL+mamQ+mamB+pSB4A5</td><td>6</td><td>30(2/23)</td><td>36</td><td>LB(CP)</td></tr>
+</table>
+</div>
+<div>
+<a name="1014" class="kyoto-jump"></a>
+<h3>10/14</h3>
+<h4>Liquid Culture</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Name</th><th>medium</th></tr>
+<tr><td>9/22 Master Plate Pcon+mamL+mamQ+mamB </td><td>LB medium(CP)</td></tr>
+<tr><td>9/22 Master Plate Pcon+mamL+mamQ </td><td>LB medium(CP)</td></tr>
+<tr><td>9/22 Master Plate Pcon+mamL </td><td>LB medium(CP)</td></tr>
+<tr><td>10/6 Transformation Pcon+ mamB </td><td>LB medium(CP)</td></tr>
+<tr><td>10/9 Transformation Pcon+ mamB </td><td>LB medium(CP)</td></tr>
+<tr><td>10/4 Transformation mamQ+pSB1C3 (E1-3) </td><td>LB medium(CP)</td></tr>
+<tr><td>9/18 Master Plate T7+RBS+pSB1C3</td><td>LB medium(CP)</td></tr>
+<tr><td>10/13 Master Plate Pcon+mamL+mamQ+pSB4A5</td><td>LB medium(Amp)</td></tr>
+</table>
+<div>
+<a name="1015" class="kyoto-jump"></a>
+<h3>10/15</h3>
+<h4>Inoculation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<p>10:45~</p>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>10/14 pLQB</td></tr>
+<tr><td>10/14 pLQ</td></tr>
+<tr><td>10/14 pL</td></tr>
+<tr><td>10/14 T7-RBS</td></tr>
+<tr><td>10/14 pLQ(4A5)</td></tr>
+</table>
+<p>12:30</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.096</td></tr>
+<tr><td>LQ</td><td>0.087</td></tr>
+<tr><td>L</td><td>0.278</td></tr>
+<tr><td>T7-RBS</td><td>0.253</td></tr>
+</table>
+<p>13:05</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.153</td></tr>
+<tr><td>LQ</td><td>0.139</td></tr>
+<tr><td>L</td><td>0.448</td></tr>
+<tr><td>T7-RBS</td><td>0.389</td></tr>
+<tr><td>pLQ(4A5)</td><td>0.277</td></tr>
+</table>
+<p>13:46</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.275</td></tr>
+<tr><td>LQ</td><td>0.204</td></tr>
+<tr><td>L</td><td>0.597</td></tr>
+<tr><td>T7-RBS</td><td>0.516</td></tr>
+<tr><td>pLQ(4A5)</td><td>0.443</td></tr>
+</table>
+<p>14:26</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.293</td></tr>
+<tr><td>LQ</td><td>0.275</td></tr>
+<tr><td>L</td><td>0.896</td></tr>
+<tr><td>T7-RBS</td><td>0.595</td></tr>
+<tr><td>pLQ(4A5)</td><td>0.641</td></tr>
+</table>
+<p>14:55</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.435</td></tr>
+<tr><td>LQ</td><td>0.434</td></tr>
+<tr><td>L</td><td>0.914</td></tr>
+<tr><td>T7-RBS</td><td>0.837</td></tr>
+<tr><td>pLQ(4A5)</td><td>0.863</td></tr>
+</table>
+<p>15:43</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>0.871</td></tr>
+<tr><td>LQ</td><td>0.826</td></tr>
+<tr><td>L</td><td>1.735</td></tr>
+<tr><td>T7-RBS</td><td>1.692</td></tr>
+<tr><td>pLQ(4A5)</td><td>1.458</td></tr>
+</table>
+<p>16:33</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>1.112</td></tr>
+<tr><td>LQ</td><td>1.046</td></tr>
+<tr><td>L</td><td>0.747</td></tr>
+<tr><td>T7-RBS</td><td>1.819</td></tr>
+<tr><td>pLQ(4A5)</td><td>1.642</td></tr>
+</table>
+<p>17:15</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>1.725</td></tr>
+<tr><td>LQ</td><td>1.613</td></tr>
+<tr><td>L</td><td>2.188</td></tr>
+<tr><td>T7-RBS</td><td>2.123</td></tr>
+<tr><td>pLQ(4A5)</td><td>2.007</td></tr>
+</table>
+<p>18:20</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>1.833</td></tr>
+<tr><td>LQ</td><td>1.712</td></tr>
+<tr><td>L</td><td>2.194</td></tr>
+<tr><td>T7-RBS</td><td>2.205</td></tr>
+<tr><td>pLQ(4A5)</td><td>2.127</td></tr>
+</table>
+<p>18:45</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>LQB</td><td>1.928</td></tr>
+<tr><td>LQ</td><td>1.808</td></tr>
+<tr><td>L</td><td>2.224</td></tr>
+<tr><td>T7-RBS</td><td>2.233</td></tr>
+<tr><td>pLQ(4A5)</td><td>2.148</td></tr>
+</table>
+</div>
+<h4>Colony PCR</h4>
+<p><span class="kyoto-author">Honda </span></p>
+<table>
+<tr><th>NameⅠ</th><th>NameⅡ</th></tr>
+<tr><td>10/6 Pcon+mamB+pSB1C3 colony_1</td><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_1(seq-2+VR)</td></tr>
+<tr><td>10/9 Pcon+mamB+pSB1C3 colony_1</td><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_2(seq-2+VR)</td></tr>
+<tr><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_1</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1(seq-2+VR)</td></tr>
+<tr><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_2</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2(seq-2+VR)</td></tr>
+<tr><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3(seq-2+VR)</td></tr>
+<tr><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4(seq-2+VR)</td></tr>
+<tr><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3</td><td>-</td></tr>
+<tr><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4</td><td>-</td></tr>
+</table>
+<div>
+<a name="1016" class="kyoto-jump"></a>
+<h3>10/16</h3>
+<h4>Electrophoresis</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<table>
+<tr><th>Lane</th><th>Colony PCR Products</td></tr>
+<tr><td>6</td><td>1kbp ladder </td></tr>
+<tr><td>7</td><td>10/6 Pcon+mamB+pSB1C3 colony_1</td></tr>
+<tr><td>8</td><td>10/6 Pcon+mamB+pSB1C3 colony_2</td></tr>
+<tr><td>9</td><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_1</td></tr>
+<tr><td>10</td><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_2</td></tr>
+<tr><td>11</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1</td></tr>
+<tr><td>12</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2</td></tr>
+<tr><td>13</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3</td></tr>
+<tr><td>14</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4</td></tr>
+<tr><td>15</td><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_1(seq-2+VR)</td></tr>
+<tr><td>16</td><td>10/13 Pcon+mamL+mamQ+pSB4A5 colony_2(seq-2+VR)</td></tr>
+<tr><td>17</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_1(seq-2+VR)</td></tr>
+<tr><td>18</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_2(seq-2+VR)</td></tr>
+<tr><td>19</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_3(seq-2+VR)</td></tr>
+<tr><td>20</td><td>10/13 Pcon+mamL+mamQ+mamB+pSB4A5 colony_4(seq-2+VR)</td></tr>
+</table>
+</div>
+<img src="https://static.igem.org/mediawiki/2014/8/83/1016electrophoresis1.jpg">
+<h4>Inoculation</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<p>15:15~</p>
+<table>
+<tr><th>Sample</th></tr>
+<tr><td>10/15 RFP-his</td></tr>
+</table>
+<p>17:15</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>RFP-his</td><th>0.354</th></tr>
+</table>
+<p>18:50</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><th>RFP-his </th><th>0.908 </th></tr>
+</table>
+<p>19:20</p>
+<table>
+<tr><th>Sample</th><th>Absorbance</th></tr>
+<tr><td>RFP-his </td><td>0.992</td></tr>
+</table>
+</div>
+<div>
+<a name="1017" class="kyoto-jump"></a>
+<h3>10/17</h3>
+<h4>Western Blotting</h4>
+<p><span class="kyoto-author">Honda</span></p>
+<p>Make the 20% acrilamid gel apray the following</p>
+<table>
+<tr><th>Lane</th><th>Sample</th><th> Volume/(&micro;l)</th></tr>
+<tr><td>2</td><td>Sample buffer</td><th>5</th></tr>
+<tr><td>3</td><td>protein marker</td><th>5</th></tr>
+<tr><td>4</td><td>10/14 Pcon+mamL+mamQ+mamB+pSB1C3</td><th>5</th></tr>
+<tr><td>5</td><td>10/14 Pcon+mamL+mamQ+pSB1C3</td><th>5</th></tr>
+<tr><td>6</td><td>10/14 Pcon+mamB+pSB1C3</td><th>5</th></tr>
+<tr><td>7</td><td>10/14 Pcon+mamL+pSB1C3</td><th>5</th></tr>
+<tr><td>9</td><td>10/14 T7+RBS+pSB1C3(Nega)</td><th>5</th></tr>
+<tr><td>10</td><td>GFP-his(protein)(10 fold dilution)</td><th>5</th></tr>
+<tr><td>11</td><td>GFP-his(protein)(10 fold dilution)(37&deg;C denature for 10 min.)</td><th>5</th></tr>
+</table>
+<p>Electrophoresis:200V 25mA 90min</p>
+<p>Transcription:50V 200mA 73min</p>
 </div>
 </html>