Difference between revisions of "Team:Warwick/Project5"

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<h2>Week 5</h2>
 
<h2>Week 5</h2>
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<p>Both of the chemically transformed plates and electrotransformed plate grew over weekend.
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<br>Lpp­ompA­zif268: colony PCR of clone 2 ok (inoculate culture to purify DNA ­ inoculate 2
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cultures, 4.5ml each. Miniprep them after making a glycerol stock).
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<br>Conducted plasmid miniprep of bacterial culture. ­ Gel electrophoresis of redone PCR ­ Pgsa worked, zf2 (all others need to be repeated at
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a later stage). ­ Running gel of miniprep restriction digestion. ­ Re­doing PCR: INP, zf2, zf14 (67oC). zf10 (69oC) ­ with DMSO (0%, 3%, 6%). ­ PCR purification of BCLA and PGSA (nanodrop returned negative, redoing). ­ Redoing PCR of INP, zf2, zf10, zf14.
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<br>Redid PCR of INP, zf10 and zf14. ­ zf14 returned positive, purified (31.8 ng/l. ­ Redoing PCR of INP and zf10. ­ Purified zf2, nanodropped.
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<span class="cd-date">Jul 27</span>
 
<span class="cd-date">Jul 27</span>

Revision as of 12:21, 19 August 2015

Warwick iGEM 2015