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. 2016 Apr 12;13(6):4636–4642. doi: 10.3892/mmr.2016.5109

Table I.

Primer design of semiquantitative RT-PCR validation.

Gene symbol Ref Seq ID Forward primer Reverse primer
GPNMB NM_002510 5′-CCTCGTGGGCTCAAATATAACAT-3′ 5′-ACTGTCCTCTGACCATGCTGT-3′
CTSK NM_000396 5′-ACTCAAAGTACCCCTGTCTCAT-3′ 5′-CCACAGAGCTAAAAGCCCAAC-3′
IGFBP6 NM_002178 5′-GAGGGGCTCAAACACTCTACG-3′ 5′-CCATCCGATCCACACACCA-3′
NT5E NM_002526 5′-CCAGTACCAGGGCACTATCTG-3′ 5′-TGGCTCGATCAGTCCTTCCA-3′
MARC1 NM_022746 5′-CCTCGCCTGGTCCTGATTTC-3′ 5′-GGCAGTAGTAGGTCCTTTGTGT-3′
LGALS12 AF222694 5′-AACCCTCGCTTCCATACCAC-3′ 5′-TCCTCATTCCCGAAGAGAAAGAG-3′
Spot14 AW272342 5′-CAGGTGCTAACCAAGCGTTAC-3′ 5′-CAGAAGGCTGGGGATCATCA-3′

Primer design of the genes identified on microarray that were randomly selected for RT-PCR validation. RT-PCR, reverse transcription-polymerase chain reaction; GPNMB, glycoprotein nmb; CTSK, cathepsin K; IGFBP6, insulin like growth factor binding protein 6; NT5E, 5′-nucleotidase ecto; MARC1, mitochondrial amidoxime reducing component 1; LGALS12, lectin, galactoside-binding, soluble, 12; Spot14 (or THRSP), thyroid hormone responsive.