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. 2012 Oct 17;40(1):417–426. doi: 10.1007/s11033-012-2076-z

Table 1.

Primer sets for PCR and PCR-RFLP used for genotyping SNPs detected in bovine MYH 3 gene

SNPS Amplified region Primer sequence (5′–3′) AT(°C) SAF (bp) PR Genotype
SNP1 Exon5 AAAGCCCGAGTATCAGAACC TCCAACAGCCTCATCAAACA 57.4 435 RSaI CC: 228, 207
CT:228, 207, 150, 78
TT:207, 150, 78
SNP2 Intron5 AAAGCCCGAGTATCAGAACC TCCAACAGCCTCATCAAACA 57.4 435 BstXI TT:435
TC:435, 339, 96
CC: 339, 96
SNP3 Intron7 TTGCTGCAAATGGCATTATT TGAGATTCCCAACAAAGAGG 59.8 447 PVUII GG:447
GC:447, 222, 225
CC: 222, 225
SNP4 Exon14 TGGAGGATTTTCAGAGGGGT TGATATGGGGTGACAAGTGG 59.3 532 RSaI CC:532
CT:532, 364, 168
TT:364, 168
SNP5 Exon14 TGGAGGATTTTCAGAGGGGT TGATATGGGGTGACAAGTGG 59.3 532 TaqI CC:433, 99
CT:433, 243, 190, 99
TT:243, 190, 99

SNPs: single nucleotide polymorphisms; SNP1 = C1878T; SNP2 = T2010C; SNP3 = G3746C; SNP4 = C7294T; SNP5 = C7315T

AT: annealing temperature, SAF: size of amplification fragment, PR: PCR-RFLP