Primer name Sequence(5’-3’) Information
MG1 ATGGAGCTTTTCGAGACC The exon1 and intron1 amplication
MG2 TATTTGGGAATGTCCACAGG The exon1 and intron1 amplication
MG3 GGCCTTAAAGCCCTAGAG The 5’-flanking region amplication
MG4 GGAAGAAGTAAGGGTTGGT The 5’-flanking region amplication
MG5 CTGTGGACATTCCCAAGTAG The 3’- flanking region amplication
MG6 AGCATTAGAAACACGCACAAA The 3’- flanking region amplication
MG7 CTATTTGGGAATGTCCACAGG The myogenin cDNA amplication
MG8 ACCAACCCTTACTTCTTCCCT Whole-mount in situ hybridization
MG9 TCCCTGCTGTCCCGTCTC Whole-mount in situ hybridization
MG10 GCACCCTGATGAACCCAA Quantitative real-time PCR assay
MG11 CTCGCTTGATGACGACACTC Quantitative real-time PCR assay
Actin1 CCTTCTTGGGTATGGAGTC Quantitative real-time PCR assay
Actin2 GTCAGCAATGCCAGGGTA Quantitative real-time PCR assay
Table 1: Primers used for myogenin gene isolation, whole-mount in situ hybridization and quantitative real-time PCRs in Siniperca chuastsi.