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Alberta NINT/27 May 2008
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[[Team:Alberta_NINT/Notebook | < Back to notebook]] | [[Team:Alberta_NINT/Notebook | < Back to notebook]] | ||
| - | [[Alberta_NINT/23_May_2008 | < Previous entry]] | + | [[Alberta_NINT/23_May_2008 | < Previous entry]] | [[Alberta_NINT/28_May_2008 | Next entry >]] |
lab work (SD): | lab work (SD): | ||
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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. | ||
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Latest revision as of 21:30, 11 October 2008
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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.
