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Used 20 uL reaction.  For plasmids, diluted to concentration 1ng/uL in EB buffer and added 1uL of each dilution to a separate PCR mix.  Diluted primers from 100uM stocks to 10uM with TE buffer.

 

PCR recipe:

Quantity
Chemical
1 uLforward primer (10uM)
1 uLreverse primer (10uM)
1 uLtemplate DNA (1 ng/uL)
10 uLPhusion High Fidelity PCR master mix
7 uLdH2O
20 uLTOTAL

 

Settings for thermocycler (program: PHUSION):

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