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. 2013 Oct 9;2013:970370. doi: 10.1155/2013/970370

Table 1.

Oligonucleotides and cycling conditions for PCR amplification of p53, bcl-2, Bax, caspase 9, caspase 3, and 18S.

Gene Primer sequences AT C Size (bp)
p53 Forward—CTG CCC ACC ACA GCG ACA GG 59°C 35 471
Reverse—AGG AGC CAG GCC GTC ACC AT
Bcl-2 Forward—GGG CTA CGA GTC GGA TAC 53°C 35 64
Reverse—AGG CTG GAA GGA GAA GAT G
Bax Forward—CGC GTG GTT GCC CTC TTC TAC TTT 59°C 35 124
Reverse—CAA GCA GCC GCT CAC GGA GGA
Caspase 9 Forward—TGC AGG GTA CGC CTT GTG CG 61°C 35 130
Reverse—CCT GAT CCC GCC GAG ACC CA
Caspase 3 Forward—AGG CCT GCC GAG GTA CAG AGC 61°C 35 255
Reverse—CCG TGG CCA CCT TCC GCT TA
18s Forward—AAG ACG AAC CAG AGC GAA AG 56°C 25 149
Reverse—GGC GGG TCA TGG GAA TAA

AT: annealing temperature; C: number of cycles during exponential phase of amplification.