Viral Hepatitis
Copyright ©The Author(s) 2005.
World J Gastroenterol. Jul 28, 2005; 11(28): 4351-4356
Published online Jul 28, 2005. doi: 10.3748/wjg.v11.i28.4351
Table 1 Primer sequences for PCR and amplification conditions for each target gene
PrimerSequenceAmplification conditionsProduct (base)
Fas5-TCAGTACGGAGTTGGGGAAG-3’Denaturation at 94 °C for 45 s,207
5-CAGGCCTTCCAAGTTCTGAG-3annealing at 63 °C for 30 s and synthesizing
at 72 °C for 1 min for 35 cycles
FasL5-GATGATGGAGGGGAAGATGA-3Denaturation at 94 °C for 45 s,203
5-TGGAAAGAATCCCAAAGTGC-3’annealing at 58 °C for 30 s and synthesizing
at 72 °C for 1 min for 30 cycles
Bax5-TTTGCTTCAGGGTTTCATCC-3’Denaturation at 94 °C for 45 s,246
5-CAGTTGAAGTTGCCGTCAGA-3’annealing at 58 °C for 30 s and synthesizing
at 72 °C for 1 min for 30 cycles
Bcl-25-CGACGACTTCTCCCGCCGCTACCGC-3’Denaturation at 94 °C for 45 s,318
5-CCGCATGCTGGGGCCGTACAGTTCC-3’annealing at 67 °C for 30 s and synthesizing
at 72 °C for 1 min for 30 cycles
c-myc5-TTCGGGTAGTGGAAAACCAG-3’Denaturation at 94 °C for 45 s,203
5-CAGCAGCTCGAATTTCTTCC-3’annealing at 58 °C for 30 s and synthesizing
at 72 °C for 1 min for 28 cycles
GAPDH5-ACCACAGTCCATGCCATCAC-3’Changed according to different target genes452
5-TCCACCACCCTGTTGCTGTA-3’