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. 2016 May 12;10:1649–1661. doi: 10.2147/DDDT.S102883

Table 1.

The primers used in qRT-PCR

Gene Primer sequence Annealing temperature (°C) Fragment size (bp)
GAPDH F:5′-GTTGTCTCCTGCGACTTCA3′ 60 293
R:5′-GCCCCTCCTGTTATTATGG3′
SIRT1 F:5′-GGAACCTTTGCCTCATCTACAT3′ 60 164
R:5′-ATTCCTTTTGTGGGCGTGG3′
Caspase-3 F:5′-TATCCTGAAATGGGCATATG3′ 60 140
R:5′-TTCCTGACTTGGTATTTCAG3′
FOXO1 F:5′-AGTGGATGGTGAAGAGCGT3′ 60 324
R:5′-GCCACTTAGAAAACTGAGACC3′
FasL F:5′-GGTGCTTGCTGGCTCACAGT3′ 60 88
R:5′-TTCACGAACCCGCCTCCTC3′
BAX F:5′-CATCGAGGTGGAGAGCGACG3′ 60 140
R:5′-GTGATGGGACTGAGTCCCGC3′
Bcl-2 F:5′-AGAAGAAGGGAGAATCACAG3′ 60 160
R:5′-CGGCATGATCTTCTGTCAAG3′

Abbreviations: F, forward; qRT-PCR, quantitative reverse transcription–polymerase chain reaction; R, reverse.