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Question: You have to amplify fixed size 3.5 kb product from...
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You have to amplify fixed size 3.5 kb product from isolated genomic DNA using forward and reverse primers below:
Primer-F: CGTTTCCCGCCTTCAGTTTAGC
Primer-R: CCCGATCTAGTAACATAGATGACACC
b.) Based on protocol we used in class for DreamTaq DNA polymerase design PCR cycling program for amplification of this fragment.
Solution
The genomic DNA is used as a template for the PCR amplification of 3.5kb product. The reactions for PCR are genomic DNA template - 50ng
Forward primer 10pm/uL
Reverse primer 10 pm/uL
MgCl2,dNTPS and 1Unit Taq DNA polymerase
The PCR condtions include denaturation, annealing and extension cycles. The annealing temperature need to standadised by checking a amplification of the desired PCR product at different temperature gradient for example temperature range of 50C/52C/54C/56C/58C/60C and higher can be checked
Initial Denaturation - 95 C for 5 min- 1 cycle
Denaturation - 95 C for 30 sec,Annealing temp. for 30 sec,Extension - 72C for 2 min - for 40 cycles
Extension 72 C for 10 min- 1 cycle
4C
The extension time is higher because the PCR product is 3500bp in length
