Team:Hawaii/Notebook/2008-07-18

From 2008.igem.org

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:*for details please look [[Team:Hawaii/Initial E. Coli Transformation|here]].
:*for details please look [[Team:Hawaii/Initial E. Coli Transformation|here]].
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=== Sequencing===
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:<strong>Grace</strong>
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:* Redid PCR reactions for GFP fusion, BB-pRL1383a, B0015, J04430, R0010
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::* Gel OK this time (95V for 50 min; ladder resolved, loading dye didn't run funny)
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::* Incorrect bands still for B0015, J04430, R0010; Krystle will redo the plasmid preps for these
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::* Correct bands for GFP fusion and BB-pRL1383a. BB-pRL1383a band faint -- why?
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:* Treated PCR products w/ [[Team:Hawaii/Protocols/ExoSAP|ExoSAP]]
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:* Determined DNA concentrations using nanodrop spectrometer
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:* Sent 11 samples to CORE Hawaii for sequencing
== Drylab Work ==
== Drylab Work ==

Revision as of 23:52, 18 July 2008

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

Things we did today

Wetlab work

PCR of pRL1383a Parts

Margaret
  • for details please look here.

Extraction of Biobricks and Transformation in DB3.1

Margaret
  • for details please look here.

Sequencing

Grace
  • Redid PCR reactions for GFP fusion, BB-pRL1383a, B0015, J04430, R0010
  • Gel OK this time (95V for 50 min; ladder resolved, loading dye didn't run funny)
  • Incorrect bands still for B0015, J04430, R0010; Krystle will redo the plasmid preps for these
  • Correct bands for GFP fusion and BB-pRL1383a. BB-pRL1383a band faint -- why?
  • Treated PCR products w/ ExoSAP
  • Determined DNA concentrations using nanodrop spectrometer
  • Sent 11 samples to CORE Hawaii for sequencing

Drylab Work

Name of Task

name of person/people who performed the task
  • Summary of task and what was done. Link to experiment for detailed notes if necessary.
  • e.g. read through papers, worked on proposal, etc.


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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