Each PCR reaction was amplified
with 25 ll of PCR reaction mix (QIAGEN PCR Kit) containing
2.5 ll of 10· buffer with 1.5 mM MgCl2, 2.5 ll of Q-Solution, 0.5 ll of 10 mM dNTP mix, 1.0 ll of 10 nM forward
and reverse primer, 1.0 ll of DNA template, 0.1 ll of
5 U/ll Taq DNA polymerase and 16.4 ll RNase-free water.
The reaction cycles were performed in a Thermal Cycle as follows:
95 C for 5 min, followed by 30 cycles of 95 C for 50 s,
60 C for 30 s, and 72 C for 2 min, with a final extension step
at 72 C for 10 min.
Each PCR reaction was amplifiedwith 25 ll of PCR reaction mix (QIAGEN PCR Kit) containing2.5 ll of 10· buffer with 1.5 mM MgCl2, 2.5 ll of Q-Solution, 0.5 ll of 10 mM dNTP mix, 1.0 ll of 10 nM forwardand reverse primer, 1.0 ll of DNA template, 0.1 ll of5 U/ll Taq DNA polymerase and 16.4 ll RNase-free water.The reaction cycles were performed in a Thermal Cycle as follows:95 C for 5 min, followed by 30 cycles of 95 C for 50 s,60 C for 30 s, and 72 C for 2 min, with a final extension stepat 72 C for 10 min.
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