1. Their are 3 steps in PCR
a. Denaturation
b. Annealing
c. Extension
2. Introns and exons are nucleotide sequences within a gene. Introns are removed by RNA splicing as RNA matures. while exons go on to be covalently bonded to one another in order to create mature mRNA.
3. A master mix usually contains a thermostable DNA polymerase, dNTPs, MgCl2, and proprietary additives in a buffer optimized for PCR
4. PCR primers are short fragments of single stranded DNA (15-30 nucleotides in length) complementary to DNA sequences that flank the target region of interest
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