Imperial College/7 September 2008
From 2008.igem.org
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===Cloning=== | ===Cloning=== | ||
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+ | =====Ongoing/Where there is spare time===== | ||
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+ | *PCR trial all genomic sequences to determine optimal conditions with Taq then produce clones with Pfu | ||
+ | *Digest with ''XbaI' and ''SpeI'' and incorporate into biobricks | ||
+ | *Follow up by assaying orientation (either with sequence internal restriction site or by using ''XbaI' and ''SpeI'', as they should only be able to cut inserts in the correct orientation) | ||
=====Monday===== | =====Monday===== | ||
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*GeneArt constructs 3, 6, 10 and 12 (EpsE gene and PgsiB-RBSspoVG in construct 3, LipA-Elastin and PgsiB-RBSgsiB in construct 6, P43-RBSspoVG and Pveg-RBSspoVG), along with all above biobricks will be transformed into Xl1-Blue ''E.coli'' | *GeneArt constructs 3, 6, 10 and 12 (EpsE gene and PgsiB-RBSspoVG in construct 3, LipA-Elastin and PgsiB-RBSgsiB in construct 6, P43-RBSspoVG and Pveg-RBSspoVG), along with all above biobricks will be transformed into Xl1-Blue ''E.coli'' | ||
*Depending on results, LacI PCR to be digested and purified ready for ligation into pSB1A2/pSB1AK3 | *Depending on results, LacI PCR to be digested and purified ready for ligation into pSB1A2/pSB1AK3 | ||
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=====Tuesday===== | =====Tuesday===== |
Revision as of 22:03, 7 September 2008
7th September 2008WetlabCloningOngoing/Where there is spare time
Monday
Tuesday
Wednesday
Thursday
Friday
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