Since the dsRNA triggers the RNAi machinery, What principles should be considered in gene silencing for dsRNA prepartion? Which region of target gene should be considered to produce dsRNA?
What are general principles for double-strand DNA (dsDNA) synthesis?
I have designed a ds DNA sequence to use as positive control for my qPCR assay, I put my forward and reverse primer sequences at start and the end of my synthetic DNA.
Does it make any problem during annealing? or it's better to add more nucleotides before my primers?