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Table 1 Primers used for Q-PCR validation

From: Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep

Gene

Primer sequence (5’-3’)

Tm (°C) a

Target size (bp)

GAPDHb

Forward: ATGCCTCCTGCACCACCA

60

76

Reverse: AGTCCCTCCACGATGCCAA

FGF10

Forward: GATCCGAGAAAGGAGCGAGG

60

554

Reverse: TCCAGGATACTGTACGGGCA

LOC443300

Forward: ACCAACACATCCCATTCGCT

60

140

Reverse: CACTCAGCGTGTCCAGTTCT

FGF18

Forward: AAGTCCGGATCAAGGGCAAG

60

98

Reverse: CACACACTCTTTGCTGGTGC

Connexin43

Forward: GTCGTGTCGTTGGTGTCTCT

60

291

Reverse: CACTCAGCGTGTCCAGTTCT

SCD

Forward: AAGAGTGGCTGAGTTTCTGGTC

60

277

Reverse: GAAAGGAAGGTGATAGGGACAA

Zo1

Forward: AGATAGCCCTGCAGCCAAAG

60

117

Reverse: GGGAGGTCAAGCAGGAAGAG

MMP2

Forward: AACGCCATCCCTGATAACCT

60

126

Reverse: GCTTCCGAACTTCACGCTC

ITGB1

Forward: AGCACGGATGAGGTGAACAG

60

407

Reverse: CCAAGGCAGGTCTGACACAT

PAG11

Forward: AGCGTCGCCTACGAATCTG

60

120

Reverse: CTCAAACCCATATTCCGTCACA

CRYAB

Forward: CACCCAGCTGGATTGACACT

60

147

Reverse: CCTCATGTTTGCCATGCACC

  1. aThe annealing temperature represents the optimal temperature during quantitative PCR.
  2. bRNA levels of GAPDH was assayed for normalization during quantitative PCR.