Team:TCU Taiwan/Notebook

From 2014.igem.org

(Difference between revisions)
Line 261: Line 261:
           <h5><font face="Trebuchet MS" size="4" color="#0879A6">other part:</font></h5>
           <h5><font face="Trebuchet MS" size="4" color="#0879A6">other part:</font></h5>
           <br>
           <br>
-
           <font face="Trebuchet MS" size="4" color="#333">Prepare Human practice (ppt)<br>
+
           <p><font face="Trebuchet MS" size="4" color="#333">Get foundation from nearby store (yeah!!!!!)<br>
-
          Practice presentation<br>
+
            Decided to have iGEM contest in local school as human practice</font></p>
-
           Design gRNA for AmpR<br>
+
           <p><font face="Trebuchet MS" size="4" color="#333">Others don’t think E.Maat is a good name, under re-consideration </font></p>
-
Discuss about project. Project Name is E.Maat for now (came up by Sharon)<br>
+
-
Order restraction enzyme(PstI、EcoRI、XbaI、SpeI) </font>
+
-
          </p>
+
         </div>
         </div>
          
          
Line 272: Line 269:
         <div align="left">
         <div align="left">
           <h5><font face="Trebuchet MS" size="4" color="#0879A6">experimental part:</font></h5>
           <h5><font face="Trebuchet MS" size="4" color="#0879A6">experimental part:</font></h5>
-
           <br>
+
           <p><br>
-
          <font face="Trebuchet MS" size="4" color="#333">Prepare for the competent cell</font>
+
            <font face="Trebuchet MS" size="4" color="#333"><li></li>Extract plasmid pSB1C3 with BBa_I13521、BBa_ K914003、BBa_ K1218011</font></p>
-
          <p><font face="Trebuchet MS" size="4" color="#333">BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:<br>
+
           <p><font face="Trebuchet MS" size="4" color="#333"><li></li>Prepare Cm. plate、LB. plate </font>
-
            Transformation ( Cas9 in pSB1C3 into DH5α)<br>
+
            </p>
-
            Incubate DH5α with pSB1C3</font></p>
+
          </p>
-
           <p><font face="Trebuchet MS" size="4" color="#333">Extract plasmid with pSB1C3 from DH5α</font></p>
+
           <p>           
           <p>           
           <h5><font face="Trebuchet MS" size="4" color="#0879A6">other part:</font></h5>
           <h5><font face="Trebuchet MS" size="4" color="#0879A6">other part:</font></h5>
           <p><br>
           <p><br>
-
             <font face="Trebuchet MS" size="4" color="#333">Get foundation from nearby store (yeah!!!!!)<br>Decided to have iGEM contest in local school as human practice</font></p>
+
             <font face="Trebuchet MS" size="4" color="#333">Something wrong with gRNA for AmpR, redesign</font></p>
-
           <p><font face="Trebuchet MS" size="4" color="#333">Others don’t think E.Maat is a good name, under re-consideration </font></p>
+
          <p><font face="Trebuchet MS" size="4" color="#333">Second project theme came out by Denise and Regina: Trogene horse. Needs later discuss to decided which one as theme( E.Maat or Trogene Horse)</font></p>
 +
           <p><font face="Trebuchet MS" size="4" color="#333">Try to get foundation from Biotechnology company on e-mail.</font></p>
 +
          <p><font face="Trebuchet MS" size="4" color="#333">Prepare for igem conference in NCTU-Formosa (ppt) </font></p>
           </p>
           </p>
         </div>
         </div>

Revision as of 14:16, 7 October 2014

 
Notebook
 

Notebook

You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well.

   
Week 1 6/22~6/28

experimental part:

Prepare for the competent cell

BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
Transformation ( Cas9 in pSB1C3 into DH5α)
Incubate DH5α with pSB1C3

Extract plasmid with pSB1C3 from DH5α

other part:

Prepare Human practice (ppt)
Practice presentation
Design gRNA for AmpR
Discuss about project. Project Name is E.Maat for now (came up by Sharon)
Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

Week 2 6/29~7/5
experimental part:

Successfully transform biobrick BBa_I13521、BBa_ K914003、BBa_ K1218011 into DH5α (plasmid: pSB1C3
Extract pSB1C3 after incubation
Use Enzyme digestion(PstI and EcoRI) to confirm whether pSB1C3 is successfully extracted
Prepared Cm. plate、LB. plate
Prepared competent cell

 

other part:

Get foundation from nearby store (yeah!!!!!)
Decided to have iGEM contest in local school as human practice

Others don’t think E.Maat is a good name, under re-consideration

Week 3 7/6~7/12
experimental part:


  • Extract plasmid pSB1C3 with BBa_I13521、BBa_ K914003、BBa_ K1218011

  • Prepare Cm. plate、LB. plate

    other part:


    Something wrong with gRNA for AmpR, redesign

    Second project theme came out by Denise and Regina: Trogene horse. Needs later discuss to decided which one as theme( E.Maat or Trogene Horse)

    Try to get foundation from Biotechnology company on e-mail.

    Prepare for igem conference in NCTU-Formosa (ppt)

    Week 4 7/13~7/19
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 5 7/20~7/26
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 6 7/27~8/2
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 7 8/3~8/7
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 8 8/10~16
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 9 8/17~8/23
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 10 8/24~8/30
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 11 8/31~9/6
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 12 9/7~9/13
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 13 9/14~9/20
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 14 9/21~9/27
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    Week 15 9/28~10/4
    experimental part:

    Prepare for the competent cell

    BoBo and Ted decided to multiply plasmid within bacteria but not PCR, like this:
    Transformation ( Cas9 in pSB1C3 into DH5α)
    Incubate DH5α with pSB1C3

    Extract plasmid with pSB1C3 from DH5α

    other part:

    Prepare Human practice (ppt)
    Practice presentation
    Design gRNA for AmpR
    Discuss about project. Project Name is E.Maat for now (came up by Sharon)
    Order restraction enzyme(PstI、EcoRI、XbaI、SpeI)

    ^
       

    ^