Team:WashU/Week10

From 2012.igem.org

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<u>Wednesday, August 1</u>
<u>Wednesday, August 1</u>
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Double transformation of GC5 cells with zeaxanthin-producing construct and TOPO PCR #2, done with a control vector as well
 
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Double transformation of GC5 cells with zeaxanthin-producing construct and TOPO PCR #2, done with a control vector as well
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Today we conducted a colony PCR of the TOPO cloning of ZCD with the fusion protein (without a his-tag).  Colony PCR showed a single band of approximately 1200bp for the sample of colony number two.  A successful colony PCR should yield amplification of ZCD with a 60bp upstream region, for a total of 1170bp.  The close agreement between the band size and the expected band suggest that colony number 2 had the correct orientation of the insert (gel below).  This colony will be grown up overnight and miniprepped in the morning.  
Today we conducted a colony PCR of the TOPO cloning of ZCD with the fusion protein (without a his-tag).  Colony PCR showed a single band of approximately 1200bp for the sample of colony number two.  A successful colony PCR should yield amplification of ZCD with a 60bp upstream region, for a total of 1170bp.  The close agreement between the band size and the expected band suggest that colony number 2 had the correct orientation of the insert (gel below).  This colony will be grown up overnight and miniprepped in the morning.  
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<u>Thursday, August 2</u>
<u>Thursday, August 2</u>
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Miniprep of colony 2 from yesterday
 
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Double transformation of GC5 cells with the miniprepped colony and zeaxanthin producing construct. Will induce with proper amounts of arabinose and IPTG at optimal concentrations once OD600 reaches 0.4
 
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Miniprep of colony 2 from yesterday
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Double transformation of GC5 cells with the miniprepped colony and zeaxanthin producing construct. Will induce with proper amounts of arabinose and IPTG at optimal concentrations once OD600 reaches 0.4
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Revision as of 14:30, 2 August 2012



Monday, July 30

Failed PCR in morning

Digestion of Z construct and tet-resistant plasmid with E and S. Run on gel

PCR using KlenTaq - worked

Transformed GC5 cells with Z-construct and U Plated cells to check tomorrow


Tuesday, July 21

Colony PCR on TOPO Ligation of Z construct to T plasmid PCR of Z and U constructs


Wednesday, August 1
Double transformation of GC5 cells with zeaxanthin-producing construct and TOPO PCR #2, done with a control vector as well Today we conducted a colony PCR of the TOPO cloning of ZCD with the fusion protein (without a his-tag). Colony PCR showed a single band of approximately 1200bp for the sample of colony number two. A successful colony PCR should yield amplification of ZCD with a 60bp upstream region, for a total of 1170bp. The close agreement between the band size and the expected band suggest that colony number 2 had the correct orientation of the insert (gel below). This colony will be grown up overnight and miniprepped in the morning.


Thursday, August 2
Miniprep of colony 2 from yesterday

Double transformation of GC5 cells with the miniprepped colony and zeaxanthin producing construct. Will induce with proper amounts of arabinose and IPTG at optimal concentrations once OD600 reaches 0.4


Friday, August 3