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. 2017 Sep 12;16(5):6683–6689. doi: 10.3892/mmr.2017.7465

Table I.

Primers used in the reverse transcription-quantitative polymerase chain reaction.

Gene Sense primer (5′-3′) Anti-sense primer (5′-3′)
SCN7A TGCTGGTCAGTGTCCTGAAG ATAGGCCATGGCAAGTATGC
DANCR GCCACTATGTAGCGGGTTTC ACCTGCGCTAAGAACTGAGG
TSIX GTGGTGGCAGGCAACTTAAT GCACATTCAGGCTCTCAACA
SSTR5-AS1 AGCCCCTCATCTTGGCTAAT TTTCCCTCTGAGCAGCAAAT
XIST TTGCATATGTGGGCAAGTGT GCTCTTGAGGCTTTTGTTGG
ENST00000433576.1 ACACTGTGGGACTTCTTAGCC TTCTGTGGTCGTGGTCTTTG
LINGO3 CGCTGCAATCTCACATCACT GCACCAGGTCTCTGAAGGAG
MPEG1 CCCCAACATGCTACCTGACT CTCCTCGTGGATCTGGGATA
SLPI CTGTGGAAGGCTCTGGAAAG AAAGGACCTGGACCACACAG
NPPB TTCTTGCATCTGGCTTTCCT TGTGGAATCAGAAGCAGGTG
RUNX2 GGTTCCAGCAGGTAGCTGAG GCCTACAAAGGTGGGTTTGA
MRC1 GGCACTTGTGGAGAAGAAGC GTGGCCTTGGTGATCTTGTT
GAPDH GGGCTGCTTTTAACTCTGGT GCAGGTTTTTCTAGACGG

SCN7A, sodium voltage-gated channel α subunit 7; DANCR, differentiation antagonizing non-protein coding RNA; XIST, X inactive specific transcript; LINGO3, leucine rich repeat and Ig domain containing 3; MPEG1, macrophage expressed 1; NPPB, natriuretic peptide B; RUNX2, runt-related transcription factor 2; MRC1, mannose receptor C-type 1.