| Literature DB >> 26199260 |
Rafijul Bari1, Sarah Schell1, MaCal Tuggle1, Wing Leung2.
Abstract
As new killer-cell immunoglobulin-like receptor (KIR) alleles are discovered, a challenge in KIR typing is maintaining sensitivity and specificity. A single nucleotide polymorphism assay can be used to type functional KIR2DL1 alleles. We improved recently on the earlier method by using a higher-specificity assay. The major modifications include the development of sequence-specific primers to selectively amplify the transmembrane domain of all known KIR2DL1 alleles via polymerase chain reaction with sequence-specific primers (PCR-SSP), and using the PCR products as the template for a revised KIR2DL1 functional allele-typing assay. This modified method allows high-throughput typing with high specificity.Entities:
Keywords: KIR polymorphism; KIR2DL1 allelotyping; KIRs genotyping; killer-cell immunoglobulin-like receptor (KIR); natural killer (NK) cell; single nucleotide polymorphism (SNP) assay
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Year: 2015 PMID: 26199260 DOI: 10.1309/LMMN1K6SBRJCGD9J
Source DB: PubMed Journal: Lab Med ISSN: 0007-5027