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. Author manuscript; available in PMC: 2017 Jun 8.
Published in final edited form as: Bio Protoc. 2017 Feb 20;7(4):e2148. doi: 10.21769/BioProtoc.2148

Table 1.

PCR setup for amplification of the RGR unit

DNA template 20 ng
dNTPs (2 mM) 10 μl
Forward primer (20 μM) 2.5 μl
Reverse primer (20 μM) 2.5 μl
5x PCR buffer 20 μl
Phusion DNA polymerase (NEB) 1 μl
Add nuclease free H2O to 100 μl