Team:Hawaii/Notebook/2008-08-15

From 2008.igem.org

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(Reconstruction of BB-pRL1383a)
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== Drylab Work ==
== Drylab Work ==
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===Name of Task===
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===Editing team website===
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:<strong> name of person/people who performed the task</strong>
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:<strong> Grace</strong>
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:* Summary of task and what was done. Link to experiment for detailed notes if necessary.
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:* e.g. read through papers, worked on proposal, etc.
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= Discussion =
= Discussion =

Revision as of 01:52, 16 August 2008

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Things we did today

Wetlab work

Reconstruction of BB-pRL1383a

EtBr stained 1% agarose gel ran at 72V for ... Thirty-five microliters of RE digested BB-pRL1383a and fifty microliters of RE digested J33207 were loaded.
Grace
  • PCR amplification of J33207
  • ExoSAP'd PCR product
  • RE digested of J33207 and BB-pRL1383a (w/ GFP)
  • Ran digests on a 1% agarose gel at 72V for 1.5 hours.
  • Ladder did not run well. Bands not resolving well.
  • Redid PCR and RE digests

Drylab Work

Editing team website

Grace

Discussion

  • DH5α does not carry lacIq; therefore, IPTG is not neccessary to induce the lac promoter.
  • IPTG is necessary for induction in DB3.1 cells.

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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