Team:Hawaii/Notebook/2008-10-22

From 2008.igem.org

(Difference between revisions)
(Extracted J04430 from filter paper)
(Wetlab work)
 
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:* Used 2 μl each of BBpRL1383a-1 and J04430 (from filter) to transform DB3.1
:* Used 2 μl each of BBpRL1383a-1 and J04430 (from filter) to transform DB3.1
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 +
===Construction of GFP secretion device===
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:<strong>Krystle</strong>
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:* Gel purify restriction digests from yesterday
 +
:* Ligate nir+rbs and slr+gfpf into restricted psB1A3 from Margaret
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:* Transformed into DH5&alpha;
= Discussion =
= Discussion =

Latest revision as of 01:06, 30 October 2008

Projects Events Resources
Sponsors Experiments Milestones Protocols
Notebook (t) Meetings (t)

Things we did today

Wetlab work

Plasmid prep of BB-pRL1383a

Grace
  • E. coli did not grow. Reinoculated.

Extracted J04430 from filter paper

Grace
EtBr stained 2% agarose gel ran at 95V for 1 hour. Ten microliters of PCR product were loaded.
  • Used 2 μl of filter paper solution for PCR to verify plasmid
  • Something is wrong with the J04430 filter spot iGEM sent us. PCR with VF2/VR primers did NOT yield the expected band ~1000bp.

Transformation

Grace
  • Used 2 μl each of BBpRL1383a-1 and J04430 (from filter) to transform DB3.1


Construction of GFP secretion device

Krystle
  • Gel purify restriction digests from yesterday
  • Ligate nir+rbs and slr+gfpf into restricted psB1A3 from Margaret
  • Transformed into DH5α

Discussion

Quote of the Day

History is the only laboratory we have in which to test the consequences of thought. - Étienne Gilson


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