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从少量血液或血清中对粒细胞特异性NA抗原进行基因分型。

Genotyping of the granulocyte-specific NA antigens from small quantities of blood or serum.

作者信息

Stein E L, Santoso S, Behrens G, Mueller-Eckhardt C, Bux J

机构信息

Institute for Clinical Immunology and Transfusion Medicine, Justus Liebig University, Giessen, Germany.

出版信息

Tissue Antigens. 1995 Jan;45(1):69-72. doi: 10.1111/j.1399-0039.1995.tb02417.x.

Abstract

To avoid the well-known shortcomings of phenotyping granulocytes for the NA antigens using NA-specific human sera, a DNA-based method to determine the NA genotype was developed. Genomic DNA was isolated from blood cells or serum, amplified by polymerase chain reaction (PCR), immobilized on nylon membrane and genotyped using digoxigenin-labeled, sequence-specific oligonucleotides (SSO). The genotyping results of whole blood samples from 54 and of serum from 20 individuals correlated perfectly with our phenotyping using the antigen capture assay MAIGA. In three cases with the phenotype "NA-null" no hybridization of the NA-specific oligonucleotides occurred. These data show that SSO is a reliable method for NA genotyping especially if only small volumes of blood or even only serum probes are available.

摘要

为避免使用NA特异性人血清对粒细胞进行NA抗原表型分析时的已知缺点,开发了一种基于DNA的方法来确定NA基因型。从血细胞或血清中分离基因组DNA,通过聚合酶链反应(PCR)进行扩增,固定在尼龙膜上,并使用地高辛标记的序列特异性寡核苷酸(SSO)进行基因分型。来自54名个体的全血样本和20名个体的血清的基因分型结果与我们使用抗原捕获试验MAIGA进行的表型分析完全相关。在3例“NA缺失”表型的病例中,未出现NA特异性寡核苷酸的杂交。这些数据表明,SSO是一种可靠的NA基因分型方法,特别是在仅有少量血液甚至仅有血清样本可用的情况下。

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