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. 2020 Apr 7;11:175. doi: 10.3389/fendo.2020.00175

Table 3.

Primers and annealing temperatures used for mRNA transcript quantification in real time QPCR analysis of liver and ovarian tissues.

Gene Accession numbers Primer Sequence (5′-3′) Annealing temperature (°C)
β-actin AB039726 Forward CCTCCATTGTTGGCAGACC 57
Reverse CCTCTCTTGCTTTGAGCCTC
GAPDH KT985226.1 Forward TGATGCTGGTGCCCTGTATGTAGT 57
Reverse TGTCCTGGTTGACTCCCATCACAA
Vtg DQ641252 Forward GAAGTGCGCATGGTGGCTTGTATT 55
Reverse AGCTGCCATATCAGGAGCAGTGAT
IGF-I GU583648.1 Forward CAGGGGCATTGGTGTGA 57.1
Reverse GCAGCGTGTCTACAAGC
ERα AY055725.1 Forward GAGGAAGAGTAGCAGCACTG 55
Reverse GGCTGTGTTTCTGTCGTGAG
ERβI AF061269.1 Forward GGCAGGATGAGAACAAGTGG 55
Reverse GTAAATCTCGGGTGGCTCTG
TRαI AY973629.1 Forward AGCCTGCCATGCCAGCC 55
Reverse CCTCCTGATCCTCGAAGACC
TRβ AY973630.1 Forward GAGGAGCAGCAGAAGACGG 55
Reverse GTTGCCTTGGGCGTTTGTGG
FSHR HM347775.1 Forward CGTCCACAATCCTACCTTCG 56
Reverse TGAGAAACGGTGATTAGCGG
Cyp19a1 (aromatase) AB009336.1 Forward TTGTGCGGGTTTGGATCAATGGTG 58
Reverse TTCCGATACACTGCAGACCCAGTT

All primers were designed and validated using Primer3 online software (Whitehead Institute of Biomedical Research, Cambridge, MA, USA).