Team:Paris Saclay/Notebook/August/28

From 2014.igem.org

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(Electrophoresis of 5 digestions of pPS5 by HindIII to check if the insert of CAD is in the right position)
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==Lab Work==
==Lab Work==
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===B - Construction of the fusion protein (color)===
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===Construction of the fusion protein (color)===
====Transformation of DH5a by PSB1C3+chromoprotein====
====Transformation of DH5a by PSB1C3+chromoprotein====
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===D - lemon scent===
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===lemon scent===
==== Electrophoresis of 5 digestions of pPS5 by HindIII to check if the insert of CAD is in the right position  ====
==== Electrophoresis of 5 digestions of pPS5 by HindIII to check if the insert of CAD is in the right position  ====
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[[File:280814 HV degisetion.jpg|300px|right]]
''by Hoang Vu''
''by Hoang Vu''
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[[File:280814 HV degisetion.jpg|300px]]
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1-5: pPS5 (pJBEI+CAD) digested by HindIII
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6: pPS1 (pJBEI+Apra), our witness
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1-5: pPS5 (pJBEI+CAD) digested by HindIII
 
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6: pPS1 (pJBEI+Apra)
 
7-8: ladder
7-8: ladder
====Electrophoresis of the same 5 PCR pooled====
====Electrophoresis of the same 5 PCR pooled====
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[[File:280814 Laetitia verif decoup.jpg|300px|left]]
''by Laetitia''
''by Laetitia''
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The totality of the 5 PCR have been used. Then, we cut the lane corresponding of the Limonene synthase gene on a UV table.
The totality of the 5 PCR have been used. Then, we cut the lane corresponding of the Limonene synthase gene on a UV table.
-
[[File:280814 Laetitia verif decoup.jpg|300px]]
 
====Purification of the PCR product of Limonene synthase (BBa762100)====
====Purification of the PCR product of Limonene synthase (BBa762100)====
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We used the kit PCR-Clean-UP to extract the DNA from the agarose gel. Elution volume : 15µl
We used the kit PCR-Clean-UP to extract the DNA from the agarose gel. Elution volume : 15µl
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 +
==Photo of the Day==
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[[File:Paris Saclay 28_august.jpg|400px|center]]
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'''Members present:'''
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* Instructors and advisors: Alice, Solenne and Sylvie.
 +
* Students: Eugène, Hoang Vu, Laëtitia, Mélanie, Romain, Sean and Terry.
{{Team:Paris_Saclay/notebook_footer}}
{{Team:Paris_Saclay/notebook_footer}}

Latest revision as of 15:28, 14 October 2014

Contents

Thursday 28th August

Lab Work

Construction of the fusion protein (color)

Transformation of DH5a by PSB1C3+chromoprotein

by Mélanie

--> a compléter

Addition of adenines at the ends of PCR fragment of chromoprotein

by Laetitia

components volumes
H2O 1 μl
Gotaq buffer 5X 1µl
dATP 1mM 2 µl
Chromoprotein gene fragment (30ng/µL) 5µL
Gotaq polymerase 1µl

1h- 70°C

Ligation of the PCR fragment of chromoprotein + AAA with pGEMTeasy

by Laetitia

components volumes
2X ligation buffer T4 DNA ligase 10 μl
pGEMTeasy 1µl
Ligation mix 7 µl
Ligase 2µL

4h - 16°C


lemon scent

Electrophoresis of 5 digestions of pPS5 by HindIII to check if the insert of CAD is in the right position

280814 HV degisetion.jpg

by Hoang Vu

1-5: pPS5 (pJBEI+CAD) digested by HindIII

6: pPS1 (pJBEI+Apra), our witness

7-8: ladder

Electrophoresis of the same 5 PCR pooled

280814 Laetitia verif decoup.jpg

by Laetitia

Gel agarose 0,8% - 100V

The totality of the 5 PCR have been used. Then, we cut the lane corresponding of the Limonene synthase gene on a UV table.


Purification of the PCR product of Limonene synthase (BBa762100)

by Laetitia We used the kit PCR-Clean-UP to extract the DNA from the agarose gel. Elution volume : 15µl


Photo of the Day

Paris Saclay 28 august.jpg

Members present:

  • Instructors and advisors: Alice, Solenne and Sylvie.
  • Students: Eugène, Hoang Vu, Laëtitia, Mélanie, Romain, Sean and Terry.

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