SBB11Ntbk-Gary Dixon: Difference between revisions
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==[[User:Gary Dixon|Gary Dixon]] 14:32, 15 February 2011 (EST)== | |||
Performing 3 PCR reactions. One for part sbb1117, and two for part sbb1127 (soeing). | |||
First, sorted out some confusion about letter R and F on oligo. R and F don't necessarily correspond to your forward and reverse oligo. So ss53r is the forward oligo for P_nmpC and ss53f is the reverse. | |||
Then diluted oligos gd031 and gd032. | |||
Then went through the standard procedure to set up PCR reactions. I have three in total. | |||
ss53r/gd031R (718bp, gp = A) | |||
gd032F/ss53f (287bp, gp = B) | |||
ss42r/ss42f (1032bp) | |||
The procedure: http://openwetware.org/wiki/Template:SBB-Protocols_PCR2 | |||
Put all three PCR reactions in the <2,000kb reaction. | |||
==[[User:Gary Dixon|Gary Dixon]] 23:59, 5 February 2011 (EST)== | ==[[User:Gary Dixon|Gary Dixon]] 23:59, 5 February 2011 (EST)== | ||
Hello World | Hello World |
Revision as of 12:32, 15 February 2011
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Gary Dixon 14:32, 15 February 2011 (EST)
Performing 3 PCR reactions. One for part sbb1117, and two for part sbb1127 (soeing).
First, sorted out some confusion about letter R and F on oligo. R and F don't necessarily correspond to your forward and reverse oligo. So ss53r is the forward oligo for P_nmpC and ss53f is the reverse.
Then diluted oligos gd031 and gd032.
Then went through the standard procedure to set up PCR reactions. I have three in total.
ss53r/gd031R (718bp, gp = A)
gd032F/ss53f (287bp, gp = B)
ss42r/ss42f (1032bp)
The procedure: http://openwetware.org/wiki/Template:SBB-Protocols_PCR2
Put all three PCR reactions in the <2,000kb reaction.
Gary Dixon 23:59, 5 February 2011 (EST)
Hello World