Team:Hawaii/Notebook/2008-09- 4

From 2008.igem.org

(Difference between revisions)
(Wetlab work)
(margaret)
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:* Transformed negative control and ligation product from Tuesday into DB3.1
:* Transformed negative control and ligation product from Tuesday into DB3.1
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== Drylab Work ==
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=== Construction of B-H-R Vector Intermediates ===
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:<strong>Margaret </strong>
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[[Image:re_gel_9_3.jpg|right|thumb|300px|Re-digest of RBS+Promoters, aada, psb3k3, psb1a3, J33207, and oriT's.]]
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:*Ran a gel of [[Team:Hawaii/Notebook/2008-09- 3|Yesterday's]] restriction digest
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:*Purified the bands that were the correct size, will re-do the others.
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:*Set up cultures of constructs that did  not appear on the gel.
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===Name of Task===
 
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:<strong> name of person/people who performed the task</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.
 

Revision as of 19:18, 5 September 2008

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Notebook (t) Meetings (t)

Things we did today

Wetlab work

Re-replacement of BB-pRL1383a MCS

Grace
EtBr stained 0.8% agarose gel ran at 60V for 1.5 hours. Thirty microliters of RE digested BB-pRL1383a were loaded onto the gel.
  • Ran last night's RE digest on agarose gel
  • Extracted J33207 and BB-pRL1383a from gel
  • Treated BB-pRL1383a w/ SAP
  • Checked DNA concentration of BB-pRL1383a (---ng/μl)
  • Ligated J33207 with BB-pRL1383a
  • Negative controls = BB-pRL1383a ligated to self, J33207 ligated to self
  • Transformed into DH5α cells

3A construction of plac+rbs

Grace
  • Ligated:
  • C0012V (SAP treated) + plac + rbs (B0034 back ligation)
  • C0012V + plac + rbs (B0034 back ligation)
  • Negative controls = C0012V (SAP treated and no SAP treatment) ligated to self, plac + rbs ligated w/o vector
  • Transformed into DB3.1 cells

Cont'd construction of GFP + TT

Krystle
  • Transformed negative control and ligation product from Tuesday into DB3.1

Construction of B-H-R Vector Intermediates

Margaret
File:Re gel 9 3.jpg
Re-digest of RBS+Promoters, aada, psb3k3, psb1a3, J33207, and oriT's.
  • Ran a gel of Yesterday's restriction digest
  • Purified the bands that were the correct size, will re-do the others.
  • Set up cultures of constructs that did not appear on the gel.



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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