Table 1 Oligonucleotides used in this study.

From: Novel selectively amplified DNA sequences in the germline genome of the Japanese hagfish, Eptatretus burgeri

Oligonucleotide

Oligonucleotide sequence (5′–3′)

Method

5Sr-1a

GAGACTGCCTGGGAATACC

Primer for PCR amplification of rDNA-related sequence

5Sr-1b

GTCTCCCATCAAGTACTAACC

TrA-2a

CAACATGATTGGTCCA

Primer for PCR amplification of genomic SSH A sequence

TrA-2b

GGGTGATTTACCTCGA

TrB-1a

GGCTCATAGAAGGAAGAAGC

Primer for PCR amplification of genomic SSH B sequence

TrB-1b

CAACATCGCCACCTACATG

EEEb6-1a

CTCAGTAAKAAACRTCG

Primer for PCR amplification of genomic SSH C sequence

EEEb6-1b

GTTAAACCACGCCCAC

Nested PCR Primer 1

TCGAGCGGCCGCCCGGGCAGGT

Primer for direct colony PCR

Nested PCR Primer 2R

AGCGTGGTCGCGGCCGAGGT

M13-F

GTAAAACGACGGCCAGT

M13-R

CAGGAAACAGCTATGAC

EEEb3-f

AAATGCTGAGCATCGCG

Insert PCR for Southern-blot hybridization

EEEb3-r

GGCCAGAGAACTTGTG

EEEb1-probe

GTTTCATGGTTATGGACCGTCGTTCCGCGTCGGCGTGTGA

Probe for slot-blot hybridization

EEEb2-probe

AAAGTTTGAGTGGTGTAAGAAGTTATAATGTTTTTTTTGAGGTGAGATGTTTATTTT

EEEo1-probe

TATCTCAAAAAGTTGTKTAYGGNTTCGGAYGAAACTTGGTGGACACGTTGG

EEEo2-probe

TGGAAGTGATTTTTTCTCCTTTTTTGTGGTCAGAAGTGGTTATTTTTCATTGTTTTT

EEPa1-probe

AAAGTGAAAAGTGCCCCCTGGTGGATGATGGAAGGA

EEPs1-probe

CGGAACTCGTCGTGCGTTTTGCACATGCGCGAACGACCCC

EEEb4-probe

CCAGCGCGATCACGTGCCGCCGAGTAGAAGATGTGCACCT

CGAGGTAAATCACCCAACATGATTGGT

EEEb5-probe

CTCATAGAAGGAAGAAGCATCACATGATGTTATATGGACATGTAGGTGGCGATGTTGG

EEEb6-probe

GGTGTGGGCGTGGTTTAACTCAGTAAGAAACGTCGAGAATGTAATTTTATAAATCG

EEEb3-f

AAATGCTGAGCATCGCG

Primer for recloning of EEEb3

EEEb3-1b

GTGCCATGTTTGGTGGTATAA