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. 2012 May 18;45(4):320–334. doi: 10.1111/j.1365-2184.2012.00822.x

Table 1.

Primers for PCR amplification

Gene GenBank Primers sequences T m (°C)
GAPDH NM_00246 Forward 5′‐TAACTCTGGTAAAGTGGATATTG‐3′
Reverse 5′‐GAAGATGGTGATGGGATTTC‐3′
58
COL1 NM_000088 Forward 5′‐GGAATGAGGAGACTCGCAACC‐3′
Reverse 5′‐TCAGCACCACCGATGTCCAAA‐3′
58
BMP2 NM_001200 Forward 5′‐ATGAAGAATCTTTGGAAGAACTAC‐3′
Reverse 5′‐GGTGATGGAAACTGCTATTG‐3′
58
vWF NM_000552 Forward 5′‐AAGAAAATAACACAGGTGAA‐3′
Reverse 5′‐TACTCTCCTCTCTCATTGAC‐3′
58
ALP NM_001177530 Forward 5′‐AGCCCTTCACTGCCATCCTGT‐3′
Reverse 5′‐ATTCTCTCGTTCACCGCCCAC‐3′
58
RUNX2 NM_001024630 Forward 5′‐GGGTAACGATGAAAATTATTCT‐3′
Reverse 5′‐TTAATTGCTCTGTGATAGGTA‐3′
58
ANGPT1 NM_001199859 Forward 5′‐ACCGAGCCTATTCACAGTAT‐3′
Reverse 5′‐ACAGTTGTCATTATCAGCATCTT‐3′
58
ANGPT2 NM_001118888 Forward 5′‐GTGATTAGACAGAACACCTATGC‐3′
Reverse 5′‐AACAGTGCTCAGAAGAATGC‐3′
58
VE‐cadherin NM_001795 Forward 5′‐GCAATAGACAAGGACATAACA‐3′
Reverse 5′‐TAGGAAGTGGACCTTGGTAT‐3′
58
VEGF‐165 AB021221 Forward 5′‐TATGCGGATCAAACCTCACCA‐3′
Reverse 5′‐CACAGGGATTTTTCTTGTCTTGCT‐3′
58