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. 2010 Jul;177(1):84–96. doi: 10.2353/ajpath.2010.090767

Table 1.

List of Primers for Quantitative Real-Time RT-PCR Experiments

Gene symbol accession Primer designation Primer sequence Product length, bp
Col4a1 NM_009931.1 Col4a1S1 forward 5′-CTGGCACAAAAGGGACGAG-3′ 238
Col4a1S1 reverse 5′-ACGTGGCCGAGAATTTCACC-3′
Col4a2 NM_009932.2 Col4a2S2 forward 5′-TGCTACCCGGAGAAAGGAG-3′ 106
Col4a2S2 reverse 5′-CTTTGCGGCCCTGTAGTCC-3′
Col4a3 NM_007734.1 Col4a3S7 forward 5′-GGGACATGTAACTACTACTCAAACTCC-3′ 88
Col4a3S7 reverse 5′-TCACAGTTGATGGAATAGGTTTTCT-3′
Col4a4 NM_007735.1 Col4a4S4 forward 5′-CTGGCTTGAAGGGAGACCT-3′ 69
Col4a4S4 reverse 5′-CTCCTGCATCACCAGGAAGT-3′
Col4a5 NM_007736.2 Col4a5 forward 5′-GGAGAACGGGGGTTTCCAG-3′ 247
Col4a5 reverse 5′-CTCCCTTGGTTCCATTGCATC-3′
Cxcl12 NM_013655.3 Cxcl12 forward 5′-CAAGGTCGTCGCCGTGCTG-3′ 122
Cxcl12 reverse 5′-CGTTGGCTCTGGCGATGTGG-3′
Cxcr4 NM_009911 Cxcr4 forward 5′-CAGAGGCCAAGGAAACTGCT-3′ 101
Cxcr4 reverse 5′-CTGACGTCGGCAAAGATGAA-3′
Cyclophilin NM_008907 cyclophilin forward 5′-CAGACGCCACTGTCGCTTT-3′ 132
cyclophilin reverse 5′-TGTCTTTGGAACTTTGTCTGCAA-3′
Egln3 NM_NM_028133.1 Egln3 forward 5′-TGTCTGGTACTTCGATGCTGA-3′ 85
Egln3 reverse 5′-AGCAAGAGCAGATTCAGTTTTTC-3′
Epas1 NM_001430 PPM03309A-200 Referenceposition457–477 164
Hif1a NM_001530 PPM03799B-200 Referenceposition700–720 160
Hif3a NM_152794 PPM05268B-200 Referenceposition1998–2018 180
Lama1 NM_008480.2 Lama1P1 forward 5′-TGTAGATGGCAAGGTCTTATTTCA-3′ 261
Lama1P1 reverse 5′-CTCAGGCAGTTCTGTTTGATGT-3′
Lama5 NM_001081171.1 Lama5P2 forward 5′-ACCCAAGGACCCACCTGTAG-3′ 169
Lama5P2 reverse 5′-TCATGTGTGCGTAGCCTCTC-3′
Lamb1-1 NM_008482.2 Lamb1-1P66 forward 5′-GGCAAACTGCAAAGTCTCG-3′ 61
Lamb1-1P66 reverse 5′-CTGGAGGTGTTCCACAGGTC-3′
Lamb2 NM_008483.2 Lamb2S2 forward 5′-GTGTGGCTTGCATAGCCCT-3′ 122
Lamb2S2 reverse 5′-TCCGATGACTATTTGGGTTGTCT-3′
Ngb NM_022414 PPM28801A-200 Referenceposition759–781 163
Vegf NM_03376 PPM03041E-200 Referenceposition2467–2487 191
Vhlh NM_000551 PPM27529A-200 Referenceposition2474–2493 190

Cxcr4 and Cxcl1233 and cyclophilin56 primers were designed based on prior published work. All other primers were designed by using Primer Bank (http://pga.mgh.harvard.edu/primerbank/; last accessed May 3, 2010) or the Roche Universal Probe Library (Roche Applied Science, Indianapolis, IN). Epas1, Hif1α, Hif3α, Ngb, Vegf, and Vhlh primers were purchased from SABiosciences (Frederick, MD) and sequences are unavailable; shown are the reference position obtained from SABiosciences for the amplicon. All amplified products resulted in the appropriate size band on agarose gels.