No Band Due to Primer Design or Synthesis Errors (PCR (Polymerase Chain Reaction))

Question

Accepted Answer

No amplification observed even with optimized reaction conditions. Primers may have incorrect sequences, poor design, or target sequence may be too long for current protocol. Common causes: 1) Primers designed or synthesized incorrectly by user or manufacturer (wrong sequence, not complementary to template) 2) Primers contain repetitive sequences or regions with high complementarity 3) Primers may amplify pseudogenes or prime unintended regions 4) Target sequence too long for current PCR component concentrations and/or cycling conditions Solutions: 1) Verify primers have correct sequence and are complementary to template 2) Use primer design program to avoid repetitive sequences and regions with high complementarity 3) Perform BLAST search to avoid primers that could amplify pseudogenes or prime unintended regions 4) Calculate Tm using oligocalc tool with default salt concentration and 0.2–1 µM primer; use lowest Tm of the primers for annealing temperature calculation 5) For long targets, reoptimize assay protocol and/or increase duration of PCR steps, especially extension step