Team:Hawaii/Notebook/2008-10-14

From 2008.igem.org

(Difference between revisions)
(Construction of secretion device (cont.))
(Wetlab work)
 
Line 15: Line 15:
::* nrsg6 (from 10/11) + BBpRL1383a-1
::* nrsg6 (from 10/11) + BBpRL1383a-1
::* J33207 + pRL1383a
::* J33207 + pRL1383a
 +
 +
===Plasmid Prep===
 +
:<strong>Krystle</strong>
 +
:* Plasmid Prepped 2 cultures of BBpRL1383
 +
:* Nanodrop concentration is 330 ng/ul
 +
:* Gel verification for plasmid shows blank lanes
==Drylab Work==
==Drylab Work==

Latest revision as of 00:57, 30 October 2008

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

Things we did today

Wetlab work

Construction of secretion device (cont.)

EtBr stained 2% agarose gel ran at 60V for 2 hours. Thirty microliters of RE digested DNA were loaded into each well.
Grace
  • Ran RE digests on gel
  • Extracted rgt1 and prpgt5 from gel
  • Ligated:
  • prpgt5 + BBpRL1383a-1
  • nir + rgt1 + BBpRL1383a-1
  • plac + rgt1 + BBpRL1383a-1
  • nrsg6 (from 10/11) + BBpRL1383a-1
  • J33207 + pRL1383a

Plasmid Prep

Krystle
  • Plasmid Prepped 2 cultures of BBpRL1383
  • Nanodrop concentration is 330 ng/ul
  • Gel verification for plasmid shows blank lanes

Drylab Work

Sequencing analysis

Grace
  • prpgt, nrsg, sgt, and pgt sequences all returned inserts of E. coli genomic DNA instead of desired construct

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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