User:University of Washington/8 July 2008

From 2008.igem.org

(Difference between revisions)
(LuxR from AraC and TetR)
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- Performed the first part of QuikChange Mutagenesis
- Performed the first part of QuikChange Mutagenesis
-
 
+
*Dilute Primers(100 pmole/ul) 1:10 ==> 10pmole/ul with deionized water.
-
 
+
*Mix(2 reactions in 2 PRC tubes))
 +
<table>
 +
<tr>
 +
<th>Materials</th><th>Reaction#1</th><th>Reaction#2</th>
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</tr>
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<tr>
 +
<td>AraC plasmid</td><td>39.3 ul</td><td>39.5 ul</td>
 +
</tr>
 +
<tr>
 +
<td>10X pfuTurbo reaction buffer</td><td>5 ul</td><td>5 ul</td>
 +
</tr>
 +
<tr>
 +
<td>dNTP mix</td><td>1 ul</td><td>1 ul</td>
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</tr>
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<tr>
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<td>primer AraC-F</td><td>AraC1F 0.806 ul</td><td>AraC2F 0.728 ul</td>
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</tr>
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<tr>
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<td>primer AraC-R</td><td>AraC1R 0.806 ul</td><td>AraC2R 0.728 ul</td>
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</tr>
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<tr>
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<td>DMSO</td><td>3 ul</td><td>3 ul</td>
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</tr>
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</table>
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*1 ul pfuTurbo
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*Temperature Cycle(There is small change from our protocol page)
 +

Revision as of 00:43, 9 July 2008

Contents

BioBrick Promoter Construct Sequencing

- Because the previous forward sequencing reaction and analysis yielded high-noise results, the forward sequencing protocol was carried out a second time.

- VF2 primer (100pmol/uL) was diluted 1 to 100 with distilled water.

- 8 uL of diluted VF2 primer (1pmol/uL) was added to four Eppendorf tubes.

- 4 uL of miniprepped plasmid DNA for parts I20260, I20268, I20269, and I20270 were added to tubes of primer, after appropriate labeling of the tubes.

- Plasmid template and VF2 primer solutions were resubmitted to the UW DNA Sequencing Facility for reaction and analysis.

- The index and middle fingers were crossed.

RP4 Conjugation

·Testing DH5α and S17-1+RP4 resistance to Chloremphenicol and Ampicillin.
·Testing S17-1 to DH5α conjugation using RP4 plasmid and conjugation protocol #1.

·Make glycerol stock of S17-1+RP4 UW Glycerol Stocks

Non-RP4 Conjugation

·Plate out CV13(Yep13) and pDPT51

LuxR from pLac

- Made glycerol stocks of R0010 and I763004.

- Miniprepped and sent in for sequencing part I763004.

LuxR from AraC and TetR

- Cells with AraC plasmid grew on Amp plate and was stored in the fridge. (Note: The cells were spread by glass rod instead of scraping using the metal rod, so single colonies can be found only on the side of the plate)

- Miniprepped 5 cultures of AraC.

- Ran gel (5 ul DNA + 2 ul dye) and found that five plasmid from 5 tubes have the same length. The plasmid was then combined into one tube.

- Nanodropped AraC plasmid: 201.6 ng/ml; 260/280 = 1.89; 260/230 = 2.17

- Performed the first part of QuikChange Mutagenesis

  • Dilute Primers(100 pmole/ul) 1:10 ==> 10pmole/ul with deionized water.
  • Mix(2 reactions in 2 PRC tubes))
MaterialsReaction#1Reaction#2
AraC plasmid39.3 ul39.5 ul
10X pfuTurbo reaction buffer5 ul5 ul
dNTP mix1 ul1 ul
primer AraC-FAraC1F 0.806 ulAraC2F 0.728 ul
primer AraC-RAraC1R 0.806 ulAraC2R 0.728 ul
DMSO3 ul3 ul
  • 1 ul pfuTurbo
  • Temperature Cycle(There is small change from our protocol page)





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