840:153g:Projects/project20/2011/11/01: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
Line 6: Line 6:
| colspan="2"|
| colspan="2"|
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
==Entry title==
==PCR Product Purification==
* After 3 gradient PCR attempts, We are unable to get proper amplification i.e single cut clear band on the agarose gel.
* After 3 gradient PCR attempts, We are unable to get proper amplification i.e single cut clear band on the agarose gel.
* We were trying to clone the PCR product containing segment which has wrongly amplified.
* We were trying to clone the PCR product containing segment which has wrongly amplified.

Revision as of 11:29, 8 December 2011

Project name <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

PCR Product Purification

  • After 3 gradient PCR attempts, We are unable to get proper amplification i.e single cut clear band on the agarose gel.
  • We were trying to clone the PCR product containing segment which has wrongly amplified.
  • For cloning, we have to purify PCR product.So initially we run 13 samples on gel and then purify using Kit based method.
  • We also directly purify the 3 PCR product without running on a gel using Kit based method.
  • Sample classification depend upon intensity of band appear previously on gel.