Team:UNICAMP-Brazil/Protocols/Preparation of electrocompetent S. cereviseae
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(New page: ==Prepare of eletrocompeten ''S. serevisiae''== 1- Grow yest strain in 50ml YEPD medium overnight, 250 RPM, 30ºC. 2- Inoculate 100 ml YEPD in a 500ml flask in a OD=0,1, 250 RPM, 30...) |
(→Prepare of eletrocompeten S. cerevisiae) |
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- | ==Prepare of eletrocompeten ''S. | + | {{:Team:UNICAMP-Brazil/inc_topo}} |
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+ | [[Team:UNICAMP-Brazil/Protocols|Back to Protocols]] | ||
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+ | ==Prepare of eletrocompeten ''S. cerevisiae''== | ||
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10- Ressuspend cells in 200ul | 10- Ressuspend cells in 200ul | ||
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+ | ==''S. cerevisiae'' Transformation== | ||
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+ | 1- In a 1,5ml tube, pipete 40ul of fresh eletrocompetent cells, and addthe DNA (5-100ng in 5ul) | ||
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+ | 2- mix gently and place on ice for 5 minutes | ||
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+ | 3- transfer the contents of the tube to a cold electroporation bucket. | ||
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+ | 4- Proceed electroporation | ||
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+ | 5- Add immediately 1ml of cold sorbitol (1M) | ||
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+ | 6- Plate in seletive media (YNB Ura- ) | ||
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+ | ==Culture Media== | ||
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+ | YEPD | ||
+ | 10g yeast extract, | ||
+ | 20g peptone, | ||
+ | 20g glucose, | ||
+ | Final volume: 1l | ||
- | + | YNB Ura- | |
+ | 6,7g YNB, | ||
+ | 30g glucose, | ||
+ | 30g agar, | ||
+ | 10ml tryptophan (100x), | ||
+ | 10ml histidine (100x), | ||
+ | 30ml leucine (100x), | ||
+ | 30ml Drop out | ||
+ | Drop out: | ||
+ | 0,5g/l Adenine | ||
+ | 1,2g/l L- aspartic acid | ||
+ | 1,2g/l L- glutamic acid | ||
+ | 0,24g/l L- arginine | ||
+ | 0,36g/l L- lysine | ||
+ | 0,24g/l L- methionine | ||
+ | 0,6g/l L- phenylalanine | ||
+ | 4,5g/l L- serine | ||
+ | 2,4g/l L- treotonine | ||
+ | 0,18g/l L- tyrosine | ||
+ | 1,8g/l L- valine | ||
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- | {{:Team:UNICAMP-Brazil/inc_rodape}} | + | {{:Team:UNICAMP-Brazil/inc_rodape}} |
Latest revision as of 14:56, 20 October 2009
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