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. 2014 Feb 20;7(5):1618–1624. doi: 10.3892/ol.2014.1897

Table I.

Conventional qPCR analyses of CXCL12, transcript variants 1–4; CXCR4, transcript variants 1–2 and CXCR7.

cDNA GenBank accession number Primer Primer sequence (5′-3′) Position PCR product size (bp)
CXCL12, transcript variant 1 NM_199168 S TACAGATGCCCATGCCGATT 174–193 262
A GCCCTTTCATCTCTCACAAGGT 414–435
CXCL12, transcript variant 2 NM_000609 S TGTGCATTGACCCGAAGCTA 301–320 144
A CAGGCCCTTCCCTAACACT 426–444
CXCL12, transcript variant 3 NM_001033886 S ACTGTGCCCTTCAGATTGTAGCC 253–275 260
A AGCAAATTTACAAAGCGCCGAGA 490–512
CXCL12, transcript variant 4 NM_001178134 S TACAGATGCCCATGCCGATT 174–193 196
A CGCTGATCAGGTTGTTTAAAG 349–369
CXCR4, transcript variant 1 NM_001008540 S CTACATTAATTCTCTTGTGCC 175–195 241
A ATTTTCTTCACGGAAACAGG 396–415
CXCR4, transcript variant 2 NM_003467 S CTGAGTGCTCCAGTAGCC 61–68 281
A TGCAGCCTGTACTTGTCC 314–331
CXCR7 NM_020311.2 S CAAAGCTGCCATCTAGAGG 16–34 252
A CTGATGTCCGAGAAGTTCC 249–267
MRLP19 (reference gene) NM_014763 S TCCTCGGGTCCAGGAGATT 529–547 58
A CAAGCTATCATCCAGCCGTTT 566–586

Oligonucleotide sequences for S and A primers. MRPL19 was the reference gene. S, sense; A, antisense; MRPL19, mitochondrial ribosomal protein L19; qPCR; quantitative polymerase chain reaction.