During Quick change SDM F and R primers are complementary of each other when performing independent Forward and reverse primer PCR reaction (In different tubes) for quick change SDM then it is Linear amplification.
During inverse PCR SDM F and R primers are designed back to back orientation and both primers are using in the same reaction (same tube) then it is exponential amplification.
Kindly explain exponential and linear amplification with respect to both kind of mutagenesis strategy?