Uppsala-Sweden/8 September 2009

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(Difference between revisions)
(New page: {{Uppsala-Sweden Template}} ==Ligation and transformatioin of antisense RNA and other stuff== Performed accordingly: Media:Assembly volume calcuator 090908.xls --~~~~)
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==Ligation and transformatioin of antisense RNA and other stuff==
==Ligation and transformatioin of antisense RNA and other stuff==
Performed accordingly: [[Media:Assembly volume calcuator 090908.xls]]
Performed accordingly: [[Media:Assembly volume calcuator 090908.xls]]
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The concentrations for the purified digestions were quite low but we decided to go for the transformation anyway.
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--[[User:Anders|Anders]] 16:29, 8 September 2009 (UTC)
--[[User:Anders|Anders]] 16:29, 8 September 2009 (UTC)
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Since we had quite low concentrations of the ligations we decided to add 20 µl of the ligation mix to the competent cells. The protocoll for the transformation was our standard one.
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1) Thaw competent cells on ice (Top 10).
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2) Add ligation mix (20µl).
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3) Let the cells sit on ice for 30 min.
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4) 55 sec heat shock, 42 deg C.
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5) 5 min on ice.
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6) Add 500 µl of SOC
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7) Incubate in shaker at 37 deg C, for 60-70 min.

Revision as of 16:50, 8 September 2009




Ligation and transformatioin of antisense RNA and other stuff

Performed accordingly: Media:Assembly volume calcuator 090908.xls The concentrations for the purified digestions were quite low but we decided to go for the transformation anyway.

--Anders 16:29, 8 September 2009 (UTC)

Since we had quite low concentrations of the ligations we decided to add 20 µl of the ligation mix to the competent cells. The protocoll for the transformation was our standard one. 1) Thaw competent cells on ice (Top 10). 2) Add ligation mix (20µl). 3) Let the cells sit on ice for 30 min. 4) 55 sec heat shock, 42 deg C. 5) 5 min on ice. 6) Add 500 µl of SOC 7) Incubate in shaker at 37 deg C, for 60-70 min.