| Literature DB >> 10852389 |
D M Dinauer1, R A Luhm, A J Uzgiris, D D Eckels, M J Hessner.
Abstract
Due to the expanding number of known HLA class II DQB1 alleles, high-resolution oligotyping is becoming ineffective, therefore a sequence-based typing (SBT) strategy was developed to provide rapid and definitive typing of HLA-DQB1. HLA-DQB1*02, *03, *04, *05, and *06 alleles were individually amplified by polymerase chain reaction (PCR) using exon 2 group-specific primers. Forward and reverse PCR primers were tailed with M13 universal and M13 reverse sequences, respectively. Subsequent bi-directional cycle-sequencing was carried out using Cy5.5-labeled M13 universal primer and Cy5.0-labeled M13 reverse primer. Automated sequencing was performed in 30 min using a Visible Genetics, Inc. (VGI) MicroGene Clipper Sequencer. Full concordance was observed between this SBT method and oligotyping among 151 individuals.Entities:
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Year: 2000 PMID: 10852389 DOI: 10.1034/j.1399-0039.2000.550411.x
Source DB: PubMed Journal: Tissue Antigens ISSN: 0001-2815