Team:WashU/Week2
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Afterwards, we grew the cells up on plates with ampicillin, picked colonies and prepared liquid cultures. Then, we prepared minipreps for all of the transformed cells and ran a gel. The results are shown below. | Afterwards, we grew the cells up on plates with ampicillin, picked colonies and prepared liquid cultures. Then, we prepared minipreps for all of the transformed cells and ran a gel. The results are shown below. | ||
- | [[file:9 and 10 gel.jpg|thumb|x350px|Agarose gel of DNA to make zeaxanthin in E. coli]] | + | [[file:9 and 10 gel.jpg|thumb|x350px|Agarose gel of DNA to make zeaxanthin in E. coli (Brian and Lucas's gel)]] |
- | [[file:1,2,3,4,5,6,7,8 gel.jpg|thumb|x350px|Agarose gel of DNA to make fluorescent proteins]] | + | [[file:1,2,3,4,5,6,7,8 gel.jpg|thumb|x350px|Agarose gel of DNA to make fluorescent proteins ("the gel master's" gel)]] |
'''Website work:''' | '''Website work:''' |
Revision as of 21:49, 7 June 2012