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Alberta NINT/27 May 2008
From 2008.igem.org
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TA0In (200bp) was synthesized commercially and placed in a vector. | TA0In (200bp) was synthesized commercially and placed in a vector. | ||
Gel-purify BBa_I0500/SpeI+PstI and TA0In?XbaI+PstI fragments from 2% agarose gel. | Gel-purify BBa_I0500/SpeI+PstI and TA0In?XbaI+PstI fragments from 2% agarose gel. | ||
| - | [[Image:NINT_WMp22.JPG | | + | [[Image:NINT_WMp22.JPG | 800 px]] |
[[Alberta_NINT/28_May_2008 | Next entry >]] | [[Alberta_NINT/28_May_2008 | Next entry >]] | ||
Revision as of 17:43, 8 July 2008
lab work (SD):
DNA digest of K102000 with SpeI + PstI. Incubated at 37 C for 1 hour.
Run on 2% agarose gel. ~3 kbp fragment expected.
Ligated K102000 with E0433 and K102000 with null_output.
lab work (JD):
Recovered Part BBA_R011 from iGEM package
Transformed XL1-B cells and plated on LB+Amp100 plates.
Created 2 O/Ns as well.
lab work (WM):
Prepare BBa_K102010 fragments for ligation.
K102010 is AraC::PromBad::TA0In
AraC::PromBad comes is in BBa_I0500/SpeI+PstI (5.6kb fragment, including plasmid)
TA0In (200bp) was synthesized commercially and placed in a vector.
Gel-purify BBa_I0500/SpeI+PstI and TA0In?XbaI+PstI fragments from 2% agarose gel.
