TABLE 1.

Primers used for amplification and sequencing of the PRLR and GHR exons 2–10 from bovine genomic DNA

PCR product	Forward (5′ → 3′)	Reverse (5′ → 3′)
PRLR
Exon 2	CAGTGTTCTTGCCTGGTGG	ACAGATGGGTGGTGTGAC
Exon 3	GCGTATGCACAGCGATGC	GATTGAAGAGAAGCAAATGC
Exon 4	GACCTCATCACTGGCCTG	GAGGTTATCAGTGTCCATTC
Exon 5	GCTTCTTGACCATTGAGCC	GATCTATCCCTAAGACAAGG
Exon 6	CACCCACTTGCTTCAGCCTAGT	GAGGCACGACTGGTTCTC
Exon 7	GACCTACATACTGGCTTCTCTGC	GCAGATTTCAGGCAGAATCC
Exon 8	CGCTACTCTGTTTGGATTGCTG	GGTGCTTGGATTATCTGTAG
Exon 9	GGCTCAGATGGTAAAGAATC	GCGACTCTATGGACTGTAG
Exon 10A	GATCTTTCCGCTGTTCTGC	GGCTGGTTCTTCTAACAGAGTC
Exon 10B	GTGACAGATAGCAACATCCTGG	CTGTCACATACGAAACCATG
GHR
Exon 2	GAGACTCTAGGGCAGCGAAA	TGTCCTCCTAGTTTGCAATTTT
Exon 3	CAAGCAAGACTTAAGTTTGG	GTAAGAACAGTAGCTTGAAC
Exon 4	CTGACAACAGCTCTGAAGC	CCACTACTGCATGACACTC
Exon 5	CTAGTCCTTGGAAATGGTAC	GCATGCACTTGGACTTTGC
Exon 6	CTGCCATAAAGTGGAAGTG	CTGGGATATGTGGTATTAAG
Exon 7	CAGAAGCACCTCATGGAGC	GTATGCCTGTGTATTGACAG
Exon 8	GTGGCTATCAAGTGAAATCATTGAC	ACTGGGTTGATGAAACACTTCACTC
Exon 9	CTGACATGGAAATTGGCTTC	CTTGATTCAGAAGTCAAGAG
Exon 10A	GGTGTGATGTTGGGGTTAGC	AGGTACCATCGCACATGTCA
Exon 10B	CTTCACTAATGTATTTGTTACATG	GTAGCACAAAATTAACACCCAC