Table 1. Primer with their sequence, length of amplification (bp) used for qRT-PCR in this study.

Gene	Sense primer	Antisense primer	Size (bp)
LPL	5′-GGGTCACCTGGTCGAAGTAT-3′	5′-CTCTCTGCAATCACACGGAT-3′	122
PPARγ	5′-GCCTAAGTTTGAGTTTGCTGTG-3′	5′-GCGGTCTCCACTGAGAATAATG-3′	97
Collage I	5′-ACTTTGCTTCCCAGATGTCC-3′	5′-CCTTGGAAACCTTGTGGACC-3′	133
oc	5′-CGCTCTGTCTCTCTGACCT-3′	5′-TCACTACCTTATTGCCCTCCT-3′	93
op	5′-GATTCTGTGGACTCGGATGAAT-3′	5′-GTAGGGACGATTGGAGTGAAAG-3′	107
Runx2	5′-GCCACTTACCACAGAGCTATT-3′	5′-GAGGCGATCAGAGAACAAACT-3′	108
osterix	5′-GCAAATGACTACCCACCCTT-3′	5′-ACGAGCCATAGGGATGAGTC-3′	148
SFRP1	5′-CCAGTTCCAGGCTTCCTAA-3′	5′-GCTTCTGGAGCACATCTTGA-3′	146
SFRP2	5′-CAAACATTTCGTTGCTCGTT-3′	5′-TCATGCAATGAGGAATGGTT-3′	115
SFRP4	5′-GGTTGCAATGAGGTCACAAC-3′	5′-ATATGTGGACACTGGCAGGA-3′	116
CyclinD1	5′- ACCCTGACACCAATCTCCTC -3′	5′- ACCCTGACACCAATCTCCTC -3′	116
Lef1	5′- ATGGAAGCTTGTTGAAACCC -3′	5′- AAGAGGTGGCAGTGACTGTG -3′	128
fzd4	5′- GCAGATCCAAATACGTGGTG -3′	5′- TGGAGGTTCATTAGGCATCA -3′	115