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. 2018 Jul 7;68(3):427–438. doi: 10.1007/s12031-018-1099-x

Table 1.

Primer and probe sequences used in real-time quantitative PCR

Target Genes Forward primer (5′-3′) Reverse primer (5′-3′) Annealing (°C)
UCP1 CCTGGCAGATATCATCAC TCACCTTGGATCTGAAGG 52
HSL GGAGCACTACAAACGCAACGA TCGGCCACCGGTAAAGAG 55
ADRB3 CAACCCGGTCATCTACTG ACCGTAGCTACACAGAAG 50
HOXC9 GCAGCAAGCACAAAGAGGA CGTCTGGTACTTGGTGTAGGG 58
PACAP ATCCAGCGGACAGGAGAGAT TCCGAGTGGCGTTTGGTAAG 55
PAC1R TTGATGACTATGAGCCCGAGT ACAAGATGACCATGGCAGTG 57
VIP CAGGAACCGGGAACAGACT TATCAGGAATGCCAGGAACT 57
VPAC1 AAGTCATTGTAGAGGCAGAT AATATGTCAAGACGGAATCAG 59
VPAC2 AGAGCCATCTCTGTGCTGGTCAA AGGTAGGCCAGGAAGCAC 57
Hydrolysis probes (5′-3′)
 VPAC2 56FAM/CAGGTAGAG/ZEN/ACCCTCCACCAGAAGCCAGTAG/3IABkFQ
 PACAP 56FAM/TCGCCCACG/ZEN/AAATCCTTAACGAAGCCTATCGAA/3IABkFQ
Reference genes Forward primer (5′-3′) Reverse primer (5′-3′)
β-actin GCTCTGGCTCCTAGCACCAT GCCACCGATCCACACAGAGT 55
GAPDH TGCACCACCAACTGCTTAG GGATGCAGGGATGATGTTC 55
RPL19 CCATGAGTATGCTCAGGCTACAG CTGATCTGCTGACGGGAGTTG 57.5
TBP CACCAATGACTCCTATGA CCAAGATTCACGGTAGATA 53
18S CGGCTACCACATCCAAGGAA GCTGGAATTACCGCGGCT 55