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Table 2 Oligonucleotide primers used for PCR amplification, sequencing and screening in this study.

From: ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase

Primer name

F/R*

Nucleotide sequence (5' → 3')

Position

Function

mo-21s

F1–3

GGTGAGAGAAGGAGGGTGAG

intron 1

amplification-sequencing of intron 2 for all alleles

mo-31r

R1,4

CCAGCACCCCGGCCAGCA

intron 3

amplification-sequencing of intron 2 /screening of 46G>A

ABO-46A-F

F4

CCAGGAAAACCAAAATGCCACA

exon 2

screening of 46G>A

ABO-106G-R

R2

TAGACTTCTGGGGCTTAGGAC

exon 3

amplification of O2 allele in intron 2

ABO-106T-R

R3

AGACTTCTGGGGCTTAGGAAC

exon 3

amplification of new hybrid allele in intron 2

ABO-inII-123F

F

GTTATCAGGGTCCTAAGGACAG

intron 2

sequencing of intron 2

ABO-inII-660R

R

CTGCCTGTTGGTCCCTTCCTC

intron 2

sequencing of intron 2

ABO-133s

F5–8

GCCCCAGAAGTCTAATGCCAG

exon 3

amplification-sequencing of introns 3 and 4

ABO-202 cons-R

R5

GGGAGGCACTGACATTATACC

intron 4/exon 4

amplification-sequencing of intron 3 (except O2, B and hybrid alleles**)

ABO-188A-R

R6,9

ATACCTTGGCAACGAGACGT

intron 4/exon 4

amplification-sequencing of hybrid allele in intron 3 and screening

ABO-220 T-R

R7,10

CCACGGTGTCAGCACCTTTGA

exon 5

amplification-sequencing of O2 allele in introns 3 and 4

ABO-220 C-R

R8,11

CACGGTGTCAGCACCTTTGG

exon 5

amplification-sequencing of B allele in introns 3 and 4

ABO-inIII-F

F9

GCTGGCCGTTACAGGGTCTG

intron 3

screening of 188G>A mutation in exon 4

ABO-inIII-425F

F

GCTGCCCTCATCTCTGTGACA

intron 3

sequencing of intron 3

ABO-inIII-672F

F

GTGCTATGGCCTCTGTTGGG

intron 3

sequencing of intron 3

ABO-inIII 916F

F

CTCTGGCAGTTGATGCTGGC

intron 3

sequencing of intron 3

mo-41s

F10,11

TAAATCCTGCTCCTAGACTAAAC

intron 3

amplification-sequencing of intron 4

ABO-inIV 170F

F

GACTTGGCCCTCGTCCTGCA

intron 4

sequencing of intron 4

ABO-inIV-429R

R

GACTAGCCTGGCCAACATGG

intron 4

sequencing of intron 4

ABO-inIV-852F

F

TAGCAACTCCATTTTCCCTCCC

intron 4

sequencing of intron 4

ABO-inIV 877R

R

GTTGGAGTAGCAGACTCATAACA

intron 4

sequencing of intron 4

ABO-inIV 1122F

F

CTCCTGAGCCTCTACAATCCT

intron 4

sequencing of intron 4

ABO-inIV 1411F

F

CTCTACGTCCCTCCCAGCCT

intron 4

sequencing of intron 4

ABO-229F

F12,13

CTACCCCCAGCCAAAGGTGC

exon 5

amplification-sequencing of all alleles in intron 5

ABO-297A-R

R12

GTTGAGGATGTCGATGTTGAAT

exon 6

amplification-sequencing of A1, A2, O1 and hybrid allele in intron 5

ABO-297G-R

R13

GTTGAGGATGTCGATGTTGAAC

exon 6

amplification-sequencing of B, O1vand O2 alleles in intron 5

mo-101s

F4,9

CCGTCCGCCTGCCTTGCAG

intron 6

internal control primer pair in screening

EPB-79R

R4,9

TACTTGTTCAGGTGGCTCTCGTC

exon 7

internal control primer pair in screening

  1. * Forward/reverse primer. ** O2, B and hybrid alleles were examined in heterozygous samples. The numeral superscripts denote primer combinations. Primers with the same number were used in the same primer mixes for amplification of ABO gene fragments.