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. 2018 Dec 20;19(3):1453–1462. doi: 10.3892/mmr.2018.9779

Table I.

Primers used in the present study.

Gene Primer Annealing temperature, °C Product size, bp
GAPDH 58 163
  F 5′-CACATGGCCTCCAAGGAGTA-3
  R 5′-TCCCCTCTTCAAGGGGTCTA-3′ 58
PCSK9 58 140
  F 5′-TGGAACTCACTCACTCTGGG-3′
  R 5′-AAGAATCCTGCCTCCTTGGT-3′ 58
Bax 58 119
  F 5′-TGATCAGAACCATCATGGGC-3′
  R 5′-GGACATCAGTCGCTTCAGTG-3′ 58
Bcl-2 58 156
  F 5′-GAAGAAGCCACCCTCAAGC-3′ 58
  R 5′-AGCAAGGACACCCGCACTC-3′
Caspase-3 58 106
  F 5′-GAGGCCGACTTCTTGTATGC-3′
  R 5′-GTTTCAGCATGGCACAAAGC-3′ 58
NF-κB 58 186
  F 5′-AGACAAATGGGCTACACCGA-3′
  R 5′-AAAGCTGAGTTTGCGGAAGG-3′ 58

F, forward; R, reverse; PCSK9, proprotein convertase subtilisin/kexin type 9; Bcl-2, B-cell lymphoma 2; Bax, Bcl-2 associated X, apoptosis regulator; NF-κB, nuclear factor-κB.