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. 2007 May 21;1(2):205–215. doi: 10.1016/j.molonc.2007.05.002

Table 1.

Primers used for RT‐PCR and qPCR analyses

Gene Specificity Forward primer 5′→3′ Reverse primer 5′→3′ Product size (bp)
TIMP‐1 All exon‐skipping variantsa Forward exon 1 CCCTAGCGTGGACATTTATC Reverse exon 6 AAGGTGACGGGACTGGAAG 648 (full‐length)
TIMP‐1 Full‐length+del‐2 Forward exon 1 CCCTAGCGTGGACATTTATC Reverse exon 3 GGTATAAGGTGGTCTGGTTG 263+134
TIMP‐1 Full‐length+del‐5 Forward exon 4 ACTTCCACAGGTCCCACAAC Reverse exon 6 AAGGTGACGGGACTGGAAG 252+127
TIMP‐1 Full‐lengthb Forward exon 2 CTTCTGGCATCCTGTTGTTG Reverse exon 3 GGTATAAGGTGGTCTGGTTG 153
TIMP‐1 Del‐2b Forward exon 1/3 CCCAGAGAGACACCAGAGTCA Reverse exon 4 GTGGGACCTGTGGAAGTATC 196
GAPDH Full‐length CAATGACCCCTTCATTGACC TTCACACCCATGACGAACAT 309
a

Except variants lacking exon 1 or 6.

b

qPCR assay.