Team:Stockholm/29 July 2010

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(Difference between revisions)
(Andreas)
(Protein expression of IgG protease from pEX)
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BL21 cultures of IgG in pEX and bFGF in original vector from plates used to inoculate for IPTG induction:
BL21 cultures of IgG in pEX and bFGF in original vector from plates used to inoculate for IPTG induction:
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A streak of colonies from the IgG plate was inoculated in two separate falcon tubes containing 12 ml LB and 24 ul ampicillin (50 mg/ml). ~10 colonies from the bFGF plate was inoculated in two separate falcon tubes containing 12 ml LB and 24 ul ampicillin (50 mg/ml). This was incubated with shake in 37 °C until OD reaches around 0.6.

Revision as of 14:57, 31 July 2010


Contents

Andreas

CPP troubleshooting

Analyzed sequencing results of our constructed CPPs (LMWP and Transportan 10). It seems like our target vector recircularizes instead of ligating with our CPP primers. Me, Johan and Nina are working on troubleshooting this, however it looks like we will soon have to synthesize our genes, since our primer ligations just don't seem to work.



Nina

Protein expression of IgG protease from pEX

BL21 cultures of IgG in pEX and bFGF in original vector from plates used to inoculate for IPTG induction:


A streak of colonies from the IgG plate was inoculated in two separate falcon tubes containing 12 ml LB and 24 ul ampicillin (50 mg/ml). ~10 colonies from the bFGF plate was inoculated in two separate falcon tubes containing 12 ml LB and 24 ul ampicillin (50 mg/ml). This was incubated with shake in 37 °C until OD reaches around 0.6.