Team:KAIST-Korea/Notebook/Diary/September

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<table>
<table>
<tr>
<tr>
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<td>Primer</td><td>Direction</td><td>Sequences</td><td>Length</td>
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<td align=center>Primer</td><td>Direction</td><td>Sequences</td><td>Length</td>
</tr>
</tr>
<tr>
<tr>
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<td>V_STAT_F</td><td>Forward(NdeI)</td><td>5’-TGTTCATATGGCTAATGTCTCAGTGGTACGAACTTCAG-3’</td><td>24bp</td>
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<td align=center>V_STAT_F</td><td>Forward(NdeI)</td><td>5’-TGTTCATATGGCTAATGTCTCAGTGGTACGAACTTCAG-3’</td><td>24bp</td>
</tr>
</tr>
<tr>
<tr>
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<td>V_STAT_R</td><td>Reverse(BamHI)</td><td>5’-TATCGGATCCGAATTTACACTTCAGACACAGAAATCAAC-3’</td><td>25bp</td>
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<td align=center>V_STAT_R</td><td>Reverse(BamHI)</td><td>5’-TATCGGATCCGAATTTACACTTCAGACACAGAAATCAAC-3’</td><td>25bp</td>
</tr>
</tr>
</table>
</table>

Revision as of 13:15, 10 September 2010

 

September 1

pREP41 vector has arrived.

-> we will do E.coli transformation and increase its number.

pREP42-GFP vector has arrived (in E.coli)

-> will incubate a day and do spreading for further experiment.

Making culture media

  1. 500mL LB broth + agar 1.5% (7.5g)
  2. Do auto clave
  3. Cool it down until it reaches 50~60℃
  4. Add ampicillin(1000x 100mg/mL) and stir
  5. putting out bubbles on culture media
  6. pouling on petri dish and wait for 1 hour

Culture

  1. Competent cell + DN10A and leave it in ice for 30min
  2. Do heat shock for 45 sec and store it in ice for 2min
  3. Stabilize it in incubator for 30 to 40min
  4. Do spreading


September ?

<STAT1>

V_STAT1 (expression)


PCR STAT1.jpg

PrimerDirectionSequencesLength
V_STAT_FForward(NdeI)5’-TGTTCATATGGCTAATGTCTCAGTGGTACGAACTTCAG-3’24bp
V_STAT_RReverse(BamHI)5’-TATCGGATCCGAATTTACACTTCAGACACAGAAATCAAC-3’25bp


PCR cycle.jpg


PCR FGFR.jpg PCR HR.jpg PCR GAS.jpg


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