Lucotte G, Sesboüé R
Regional Center of Neurogenetics, Maison Blanche Hospital, 45, rue Cognacq-Jay, Reims, France.
Mol Cell Probes. 1999 Oct;13(5):389-91. doi: 10.1006/mcpr.1999.0264.
A polymerase chain reaction (PCR) assay was used to detect the two most common alpha-1-antitrypsin (A1AT) deficiency variants, S and Z. By co-amplification using primers for both the S and Z mutations, we were able to detect heterozygous and homozygous genotypes for both mutations and normal type M in a single duplex reaction. We validated our assay by comparison with phenotype studies obtained by the standard isoelectrofocusing technique.
采用聚合酶链反应(PCR)检测两种最常见的α-1-抗胰蛋白酶(A1AT)缺乏变异体S和Z。通过使用针对S和Z突变的引物进行共扩增,我们能够在一次双重反应中检测出两种突变的杂合子和纯合子基因型以及正常的M型。我们通过与标准等电聚焦技术获得的表型研究进行比较,验证了我们的检测方法。