Table 1

Location of DNA regions and oligonucleotide primer pairs for PCR amplification of genomic DNA for preparation of reporter plasmid constructs

DNA regionsPosition*5′-primer3′-primer
−8.8 −10536: −6495 ATCTGGGAGAAGGAATGGCCAGCATT TGGGCTCTCGTTAGCTCCTATGTTCTTTAGT 
−5.5 −6209: −4687 (none)  
−3.8 −3982: −3281 (none)  
+2.0 +1823: +2597 (none)  
+5.8 +4602: +7196 ATTTCCCTTCTTCTCACTTTGGGTTTAATTTG ATACTGGAGCAAGGAAAGGTCACCAGACAAT 
+11.5 +10803: +12797 TGTTTACAGAAGCTTTGTTGCTAGTGGCCC ATCAGCCCGACTGCTCCTGCAGACTCT 
DNA regionsPosition*5′-primer3′-primer
−8.8 −10536: −6495 ATCTGGGAGAAGGAATGGCCAGCATT TGGGCTCTCGTTAGCTCCTATGTTCTTTAGT 
−5.5 −6209: −4687 (none)  
−3.8 −3982: −3281 (none)  
+2.0 +1823: +2597 (none)  
+5.8 +4602: +7196 ATTTCCCTTCTTCTCACTTTGGGTTTAATTTG ATACTGGAGCAAGGAAAGGTCACCAGACAAT 
+11.5 +10803: +12797 TGTTTACAGAAGCTTTGTTGCTAGTGGCCC ATCAGCCCGACTGCTCCTGCAGACTCT 
*

Position is presented by location relative to the ATG translation start site of exon 1 in ABO on genomic DNA of NCBI reference sequence NT_035014.4.

DNA regions −5.5, −3.8, and +2.0 were prepared from human genomic clone HG-1.

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