I had subcloning my three genes in pNUS-HcN vector using NEBuilder kit and I got conformation using restriction enzymes which I used them to cut the vector and also I confirmed that using PCR amplification using Phusion enzyme and but when I sent my samples to the sequencing they were so bad, I sent my samples with Forward primer from pNUS and reverse primer from pNUS. ANY suggestion why sequencing samples went wrong please.

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