SBB11Ntbk-Xin Xin Lin: Difference between revisions

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3. Regular Zymo Cleanup- Followed Protcol
3. Regular Zymo Cleanup- Followed Protcol


   Eluted Cleaned DNA in 33uL ddH2O- Stored in 140L BoxA
   Eluted Cleaned DNA in 33uL ddH2O- Stored in 140L Box A


==[[User:Xin Xin Lin|Xin Xin Lin]] 14:07, 15 February 2011 (EST)==
==[[User:Xin Xin Lin|Xin Xin Lin]] 14:07, 15 February 2011 (EST)==

Revision as of 13:07, 18 February 2011

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Xin Xin Lin 15:01, 18 February 2011 (EST)

Work done on 2/17/11:

1. Run Analytical Gel of PCR Product

  2uL PCR Product in 5uL Loading Buffer
  Load 5uL DNA Ladder & 8uL PCR Samples- Run at 180V

2. Upload Gel Image- fadR, cspE, & cspG in lanes 4,5,&6 of Analytical Gel Image 1

  PCR Products Visible- ~767 & 2 432bp Bands

3. Regular Zymo Cleanup- Followed Protcol

  Eluted Cleaned DNA in 33uL ddH2O- Stored in 140L Box A

Xin Xin Lin 14:07, 15 February 2011 (EST)

1. PCR with P_fadR, P_cspE, & P_cspG

  Diluted fadR-F & fadR-R Oligos with 243 and 298uL ddH2O to 100uM
  Made 1:10 Dilution- 1uL 100uM Oligos in 9uL ddH2O to 10uM Dilution
  P_cspE & P_cspG Oligos already diluted to 10uM- ss39f&r for P_cspE and ss40f&r for P_cspG
  Used E.coli MG1655 Genomic DNA as Template- Used Expand Buffer & Expand Polymerase 1
  PCR Products should be 767, 432, & 432bp respectively- Used 2K55 PCR Program b/c PCR Products<2000bp