1) In the first project PCR you add 20pmol of a forward primer and 20pmol of a reverse primer. Assume that both primers are 20bp long and have the following composition: 5G, 5C, 5A, 5T. Further assume that none of the other PCR components will become limiting, the enzyme is forever active and you can run as many cycles as you need until the primers are exhausted. Further, you only obtain one PCR product of 200bp. How many DNA molecules have you produced? How many gram of DNA have you produced if the PCR product has an equal number of A,T G and C?
2) Why does 1 absorbance unit at 260nm of
a) dsDNA equal to 50 ug per ml
c) Oligonucleotides equal 20 ug per ml.













