Kafatos:dsRNA Production by PCR: Difference between revisions

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  forward primer (10 pmol/μl)    1 µl
  forward primer (10 pmol/μl)    1 µl
  reverse primer (10 pmol/μl)    1 µl
  reverse primer (10 pmol/μl)    1 µl
  H2O                            40.3 μl  
  ddH2O                          40.3 μl  
  '''Total:                          50 μl'''
  '''Total:                          50 μl'''
 
 
cDNA should be used as PCR template, but genomic DNA (at 1 μg/μl) is acceptable if the targeted region does not contain an intron and you are confident of the gene architecture.<BR>
cDNA should be used as PCR template, but genomic DNA (at 1 μg/μl) is acceptable if the targeted region does not contain an intron and you are confident of the gene architecture.<BR>


=== Purification of PCR product ===  
=== Purification of PCR product ===  
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