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. 2014 Apr 13;92(8):859–869. doi: 10.1007/s00109-014-1147-0

Table 1.

Primers and Taqman assays used

Genotyping primers
 B5-Fwd 5′-ACGCGTCGACCTTGTGTTAGTAATTCAGCC-3′
 mT4-Rev 5′-CAGAGTATGTAAGTCCAGCAGC-3′
 LacZ-Rev 5′-GGGACGACGACAGTATCGGCCT-3′
RT-PCR primers
 BGAL-FwdNew 5′-GCACGGTTACGATGCGCCCA-3′
 BGAL-RevnNew 5′-GCGCTGGAGTGACGGCAGTT -3′
 mT1-For 5′-TATTTCCTTCGCCAGTCCCTG-3′
 mT4R-Rev 5′-CAGAGTATGTAAGTCCAGCAGC-3′
 mHPRT1-For 5′-GCTTGCTGGTGAAAAGGACCTCTCGAAG-3′
 mHPRT1-Rev 5′-CCCTGAAGTACTCATTATAGTCAAGGGCAT-3′
TaqMan gene Assay ID
HO-1 Mm00516005_m1
BNP Mm01255770_g1
p53 Mm00519571_m1
Rn18s Mm03928990_g1

The genotyping primers were used to verify the presence of FtMt gene or of LacZ gene in the FtMt locus. RT-PCR primers were used for identification of the transcripts of FtMt, β-Gal, and HPRT1 in the testis of the mice. The TaqMan gene expression assays were used to quantify HO-1, BNP, p53, and Rn18s transcripts in the heart of the treated mice