SBB11Ntbk-Xin Xin Lin: Difference between revisions
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==[[User:Xin Xin Lin|Xin Xin Lin]] 13:45, 22 February 2011 (EST)== | |||
1. EcoRI/BamHI Digestion | |||
8uL Eluted PCR Product in 1uL NEB 2 Digestion Buffer w/ 1uL EcoRI & 1uL BamHI | |||
Incubate in 37 C Thermocycler for 1 Hour | |||
2. Run Preparative Gel | |||
Cut out Digested Bands & Gel Purify | |||
Place gel in 600uL ADB Buffer | |||
==[[User:Xin Xin Lin|Xin Xin Lin]] 15:01, 18 February 2011 (EST)== | ==[[User:Xin Xin Lin|Xin Xin Lin]] 15:01, 18 February 2011 (EST)== |
Revision as of 11:45, 22 February 2011
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Xin Xin Lin 13:45, 22 February 2011 (EST)
1. EcoRI/BamHI Digestion
8uL Eluted PCR Product in 1uL NEB 2 Digestion Buffer w/ 1uL EcoRI & 1uL BamHI
Incubate in 37 C Thermocycler for 1 Hour
2. Run Preparative Gel
Cut out Digested Bands & Gel Purify
Place gel in 600uL ADB Buffer
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