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. 2018 Jan 10;38(1):BSR20171109. doi: 10.1042/BSR20171109

Table 1. Primers used in the qRT-PCR assay.

Gene Primer sequence Fragment length Annealing temperature
Col10a1 F: 5′-GATCATGGAGCTCACGGAAAA-3′ 63 bp 60°C
R: 5′-CCGTTCGATTCCGCATTG-3′
Col2a1 F: 5′-GGTGGAGCAGCAAGAGCAA-3′ 83 bp 60°C
R: 5′-CGTCGCCGTAGCTGAAGTG-3′
Aggrecan F: 5′-ACTGAAGGACAGGTTCGAGTG-3′ 133 bp 60°C
R: 5′-CACACCGATAGATCCCAGAGT-3′
Pparγ F: 5′-ACCACGGTTGATTTCTCCAG-3′ 242 bp 60°C
R: 5′-GCTTTATCCCCACAGACTCG-3′
Sox9 F: 5′-GTGCTGAAGGGCTACGACTGGA-3' 159 bp 64°C
R: 5′-GTTGTGCAGATGCGGGTACTGG-3′
Mmp13 F:5'-GAGTTGGACTCACTGTTGGTC-3' 216 bp 58°C
R: GCAAGAGTCACAGGATGGTAG-3'
β-actin F: 5′-GCTGTGTTGTCCCTGTATGC3′ 106 bp 56°C
R: 5′-GAGCGCGTAACCCTCATAGA3′
Rno-miR-27a-3p RMIRQP0359GeneCopoeia, China - 60°C
Rno-miR-27b-3p RMIRQP0361GeneCopoeia, China - 60°C
Rat-U6 RMIRQP9003GeneCopoeia, China - 60°C