| Literature DB >> 11169258 |
D Sayer1, R Whidborne, B Brestovac, F Trimboli, C Witt, F Christiansen.
Abstract
The HLA-DRB1 sequencing based typing strategies reported to date require separate amplifications of each sample with a series of group-specific primers followed by sequencing of any resulting polymerase chain reaction (PCR) products. Whilst this results in high resolution typing in the majority of cases, a number of unnecessary amplifications are performed. We report here a novel approach where amplification of the second exon of HLA-DRB1 is performed in a single tube for all alleles. Retrospective analysis of 642 consecutive Western Australian unrelated bone marrow registry donors has shown that this approach results in unambiguous typings in 71.1% of cases. Ambiguities can be readily resolved if necessary with a single additional sequencing reaction on the original PCR product.Entities:
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Year: 2001 PMID: 11169258 DOI: 10.1034/j.1399-0039.2001.057001046.x
Source DB: PubMed Journal: Tissue Antigens ISSN: 0001-2815