Christopher Anderson Notebook

From 2007.igem.org

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(JCAnderson 21:35, 20 August 2007 (EDT))
(JCAnderson 11:56, 9 September 2007 (EDT))
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==[[User:JCAnderson|JCAnderson]] 11:56, 9 September 2007 (EDT)==
==[[User:JCAnderson|JCAnderson]] 11:56, 9 September 2007 (EDT)==
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Alright, that took a while.  What ended up working was taking the yfbE-pir composite part (no rbs), dropping that in the pSC101 plasmid, then doing EIPCR with dt013/14, and transforming a whole lot of material by electroporation.  I only had about 50 members to the library in the end, but there were plenty of hits in there.  I'm not sure how many, because transforming the lib with pBACr-AraGFP came out severely contaminated.  I was able to find green colonies, though, and picked 8 of them, plating with and without iron (and Ara to turn on GFP).  Several of those look nice and tight.
Alright, that took a while.  What ended up working was taking the yfbE-pir composite part (no rbs), dropping that in the pSC101 plasmid, then doing EIPCR with dt013/14, and transforming a whole lot of material by electroporation.  I only had about 50 members to the library in the end, but there were plenty of hits in there.  I'm not sure how many, because transforming the lib with pBACr-AraGFP came out severely contaminated.  I was able to find green colonies, though, and picked 8 of them, plating with and without iron (and Ara to turn on GFP).  Several of those look nice and tight.

Revision as of 15:57, 9 September 2007

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JCAnderson 21:35, 20 August 2007 (EDT)

I'm going to finish off the iron-pir construct David started. I set up a DT013/DT014 EIPCR on I716119 Clone 1 with 4K55 Expand. I716119 is the promoter-pir construct with no rbs in pBca9145. The oligo will put in an rbs library. i'll sub with SpeI/DpnI tomorrow.

JCAnderson 11:56, 9 September 2007 (EDT)

BerkiGEM2007JCA090907image1.jpg

Alright, that took a while. What ended up working was taking the yfbE-pir composite part (no rbs), dropping that in the pSC101 plasmid, then doing EIPCR with dt013/14, and transforming a whole lot of material by electroporation. I only had about 50 members to the library in the end, but there were plenty of hits in there. I'm not sure how many, because transforming the lib with pBACr-AraGFP came out severely contaminated. I was able to find green colonies, though, and picked 8 of them, plating with and without iron (and Ara to turn on GFP). Several of those look nice and tight.