I didn't get PCR product using general protocol.
Article Erratum to: Distribution and phylogenetic diversity of cbbM ...
used TaKaRa Ex Taq (Takara bio inc.). The composition of the PCR mixture is:
TaKaRa Ex Taq (5 U/μl) 0.25 μl
10×Ex Taq Buffer 5 μl
dNTP Mixture (2.5 mM each) 4 μl
Template DNA <100 ng
cbbM343F 0.2 μM(final conc.)
cbbM1126R 0.2 μM(final conc.)
ddh2O up to 50 μl
Am received from the Author, Thanks for your Support.
But its doesn't work, any other idea to improve the PCR product.
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