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Table 2 PCR primers and reaction conditions for identification of recombinant adenoviruses

From: DNA Polymerases as targets for gene therapy of hepatocellular carcinoma

gene detected

primer sequence

PCR reaction condition

product size(bp)

miR-polα-δ-ε

F: 5-AGATCTGATCCAAGAAGGTATATTGCTGTTGACAGTGAGCG-3

95°C , 5 min; 94°C , 30s, 50°C , 30s, 72°C , 45 s, 35 cycles; 72°C , 5 min

142, 284, 426

R: 5-GGATCCATCGTAGCCCTTGAAGTCCGAGGCAGTAGGCA-3

polyA

F: 5-AGATCTTGTGCCTTCTAGTTGCCAGC-3

95°C , 5 min; 94°C , 30s, 53°C , 30s, 72°C , 30s, 35 cycles; 72°C , 5 min

237

R: 5-GGATCCGCCATAGAGCCCACCGCATC-3

AFP promoter

F: 5-AGATCTCAGATTGAATTATTTGC-3

95°C , 5 min; 94°C , 30s, 55°C , 30s, 72°C , 90s, 35 cycles; 72°C , 5 min

1018

R: 5-GGATCCAAATCATGCTGAAATT-3

recombinant caspase3

F: 5-AGATCTGGCTAACTAGAGAACCCA-3

95°C , 5 min; 94°C , 30s, 58°C , 30s, 72°C , 60s, 35 cycles; 72°C , 5 min

610

R: 5-GGATCCCCCATCAACTTCATCGTGATAAAAATAGAGTTC-3

  1. The bold italics indicate restriction endonuclease sites for cloning.