Table 1.

Synthetic Oligonucleotides for Analysis of Rh50 Glycoprotein Gene

Category*Sequence nt Position-151Location
I. cDNA PCR  
 3′-UTa 5′-AATGGGAAAGGAAGCTGGAGAGCA-3′  1321-1298  3′-UTR 
 Ex-1s  5′-AGTGTGCCTCTGTCCTTTGCCACA-3′  −27-−4 Exon 1  
 Ex-4s  5′-GAAGAGTCCGCATACTACTCAGAC-3′ 601-624  Exon 4  
 Ex-5a 5′-CTGTTTGTCTCCAGGTTCAGCAAT-3′  708-605  Exon 5 
 Ex-10a  5′-CCATGTCCATGGAACTGATTGTCA-3′  1256-1233 Exon 10  
II. Genomic PCR  
 5′P2 5′-TCCAGCTTTGCTTGACTGATTGCC-3′  −679-−656  5′ region 
 5′P3  5′-CACAGGCTGTGAGATGTTGATAAG-3′  −36-−54 5′ region  
 1Ps  5′-AGAACGACAATTAGATTACAGAGC-3′ −202-−179  5′ region  
 In-1a 5′-CAAAGAGCTCAAGGGTTTATAGTA-3′  72-95  Intron 1 
 In-1s 5′-TCCTAGTGTGTTATACAAAGGTGG-3′ 111-88 Intron 1 
 In-2a 5′-AACACTCTGGCTTCATGACCTGGT-3′  117-130  Intron 2 
 In-2s  5′-TGGTGGGAGATGGGATTGCACTTT-3′  57-80 Intron 2  
 In-3a  5′-CAAGATTTGCTCCCATATACCGTA-3′ 72-95  Intron 3  
 In-3s 5′-ATTGACTTTCCTCCCATAAATGAG-3′  46-69  Intron 3 
 In-4a  5′-CTGGCTTGGATGTTCTTTTTGAGC-3′  81-104 Intron 4  
 In-4s  5′-TGACAGAGGGACACTCCATCTCAA-3′ 101-124  Intron 4  
 In-5a 5′-CAGCAGTGATGCAGAAATTACCTA-3′  67-90  Intron 5 
 In-5s  5′-TTTCAACTGAAGAATGTGATGTGG-3′  85-107 Intron 5  
 In-6a  5′-CCAAAAAGAAGGCAAATGGTCTCC-3′ 111-134  Intron 6  
 Ex-6a 5′-AGTCAGGAACTTGTATCCAAGCAC-3′  945-922  Exon 6 
 In-6s  5′-GCCCAGCTATAGCTGTGTTTCAGT-3′  57-80 Intron 6  
 In-7a  5′-CTAATGATCTTCTCTCAGGCGCGT-3′ 129-152  Intron 7  
 In-7s 5′-ATGTTACACTCTGGCCTGAAGATG-3′  21-44  Intron 7 
 In-8a  5′-ACTGCCAGAAGTTTAGAACATTTT-3′  91-114 Intron 8  
 In-8s  5′-TGTTCTAAACTTCTGGCAGTAAAG-3′ 111-134  Intron 8  
 In-9a 5′-CCTACCATGCCAGGCTAACTCAAT-3′  101-124  Intron 9 
 In-9s  5′-TCCCAGTTCTTTCCAAGCTTGAAT-3′  95-118 Intron 9  
 3′-UTa  5′-AATGGGAAAGGAAGCTGGAGAGCA-3′ 1321-1298  3′ region 
Category*Sequence nt Position-151Location
I. cDNA PCR  
 3′-UTa 5′-AATGGGAAAGGAAGCTGGAGAGCA-3′  1321-1298  3′-UTR 
 Ex-1s  5′-AGTGTGCCTCTGTCCTTTGCCACA-3′  −27-−4 Exon 1  
 Ex-4s  5′-GAAGAGTCCGCATACTACTCAGAC-3′ 601-624  Exon 4  
 Ex-5a 5′-CTGTTTGTCTCCAGGTTCAGCAAT-3′  708-605  Exon 5 
 Ex-10a  5′-CCATGTCCATGGAACTGATTGTCA-3′  1256-1233 Exon 10  
II. Genomic PCR  
 5′P2 5′-TCCAGCTTTGCTTGACTGATTGCC-3′  −679-−656  5′ region 
 5′P3  5′-CACAGGCTGTGAGATGTTGATAAG-3′  −36-−54 5′ region  
 1Ps  5′-AGAACGACAATTAGATTACAGAGC-3′ −202-−179  5′ region  
 In-1a 5′-CAAAGAGCTCAAGGGTTTATAGTA-3′  72-95  Intron 1 
 In-1s 5′-TCCTAGTGTGTTATACAAAGGTGG-3′ 111-88 Intron 1 
 In-2a 5′-AACACTCTGGCTTCATGACCTGGT-3′  117-130  Intron 2 
 In-2s  5′-TGGTGGGAGATGGGATTGCACTTT-3′  57-80 Intron 2  
 In-3a  5′-CAAGATTTGCTCCCATATACCGTA-3′ 72-95  Intron 3  
 In-3s 5′-ATTGACTTTCCTCCCATAAATGAG-3′  46-69  Intron 3 
 In-4a  5′-CTGGCTTGGATGTTCTTTTTGAGC-3′  81-104 Intron 4  
 In-4s  5′-TGACAGAGGGACACTCCATCTCAA-3′ 101-124  Intron 4  
 In-5a 5′-CAGCAGTGATGCAGAAATTACCTA-3′  67-90  Intron 5 
 In-5s  5′-TTTCAACTGAAGAATGTGATGTGG-3′  85-107 Intron 5  
 In-6a  5′-CCAAAAAGAAGGCAAATGGTCTCC-3′ 111-134  Intron 6  
 Ex-6a 5′-AGTCAGGAACTTGTATCCAAGCAC-3′  945-922  Exon 6 
 In-6s  5′-GCCCAGCTATAGCTGTGTTTCAGT-3′  57-80 Intron 6  
 In-7a  5′-CTAATGATCTTCTCTCAGGCGCGT-3′ 129-152  Intron 7  
 In-7s 5′-ATGTTACACTCTGGCCTGAAGATG-3′  21-44  Intron 7 
 In-8a  5′-ACTGCCAGAAGTTTAGAACATTTT-3′  91-114 Intron 8  
 In-8s  5′-TGTTCTAAACTTCTGGCAGTAAAG-3′ 111-134  Intron 8  
 In-9a 5′-CCTACCATGCCAGGCTAACTCAAT-3′  101-124  Intron 9 
 In-9s  5′-TCCCAGTTCTTTCCAAGCTTGAAT-3′  95-118 Intron 9  
 3′-UTa  5′-AATGGGAAAGGAAGCTGGAGAGCA-3′ 1321-1298  3′ region 

*Sense (s) and antisense (a) primers to 3′-UT, exon (Ex), 5′-region (P) and intron (In) are denoted.

F0-151

Nucleotide positions of exon primers are accounted from the first base of initiation codon ATG, whereas intron primers are designated by their distance from the exons they encompass.

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