Team:Hawaii/Notebook/2008-07-28

From 2008.igem.org

(Difference between revisions)
(New page: {{Team:Hawaii/Header}} = Things we did today = == Wetlab work == ===Transformation=== :<strong> Margaret</strong> :*Transformation of I14032 into Db3.1 ===Colony PCR=== :<strong> Margar...)
m
Line 12: Line 12:
:*Verifying the inserts of two I51020 (the base vector) and one colony of pSB1A7 (an insulated vector with high copy #)
:*Verifying the inserts of two I51020 (the base vector) and one colony of pSB1A7 (an insulated vector with high copy #)
-
===[[Team:Hawaii/PCR Amplification of pRL1383a|PCR amplification of pRL1383a===
+
===[[Team:Hawaii/PCR Amplification of pRL1383a|PCR amplification of pRL1383a]]===
:<strong> Margaret</strong>
:<strong> Margaret</strong>

Revision as of 22:04, 28 July 2008

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

Things we did today

Wetlab work

Transformation

Margaret
  • Transformation of I14032 into Db3.1

Colony PCR

Margaret
  • Verifying the inserts of two I51020 (the base vector) and one colony of pSB1A7 (an insulated vector with high copy #)

PCR amplification of pRL1383a

Margaret
  • The omega region from pSMC121 and the rep/mob region are giving primer dimers and misamplification respectively. I am trying a gradient PCR from 49°C to 55°C to see if this will fix the problem.


Drylab Work

Primer Design

Margaret
  • I want to design primers for some replication proteins + origin from pSB2K3

Discussion

Quote of the Day

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


[http://manoa.hawaii.edu/ Sponsor_UHM.gif][http://manoa.hawaii.edu/ovcrge/ Sponsor_OVCRGE.gif][http://www.ctahr.hawaii.edu Sponsor_CTAHR.gif]