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快速单样本基因分型以预测红细胞抗原表达。

Rapid, single-subject genotyping to predict red blood cell antigen expression.

作者信息

Slezak S L, Adams S, Lee-Stroka H, Martin J E, Caruccio L, Stroncek D F

机构信息

Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD 20892-1184, USA.

出版信息

Immunohematology. 2008;24(4):154-9.

Abstract

Genotyping is useful to predict the expression of those RBC antigens for which antisera are difficult to obtain and to determine the probable phenotype of highly transfused patients, and it can be used to test stored DNA when a blood sample is not available. This study assessed a sequence-specific primer (SSP)-based genotyping system for blood group alleles suitable for the rapid testing of a small number of samples and assessed the use of stored whole blood. Genomic DNA was isolated from fresh and 1- and 2-week-old stored blood from 20 donors with known ABO and Rh phenotypes and was used for ABO, RHD, and RHCE genotyping using SSPs. The amplicons were analyzed using gel electrophoresis and a novel microfluidic on-chip electrophoresis system. Analysis of DNA from fresh and 1- and 2-week-old blood by SSP and gel electrophoresis yielded the correct ABO, RHD, and RHCE type in all samples, but with DNA from 2-week-old stored blood the amplicons were more difficult to visualize. Analysis of the same samples with the SSP on-chip electrophoresis assay correctly typed all samples except for one RHCE typing discrepancy of a fresh sample and one RHCE typing discrepancy of a 2-week-old sample. Analysis of amplicons by on-chip electrophoresis required one tenth the DNA that gel electrophoresis did and could be completed within 30 minutes compared with 2 hours with gel electrophoresis. Amplicons were also more readily visualized with on-chip electrophoresis. Fresh and 1- and 2-week-old samples could be ABO and RH genotyped with SSP. Analysis using on-chip electrophoresis was easier and more rapid than that using gel electrophoresis, but test reliability was slightly more variable.

摘要

基因分型有助于预测那些难以获得抗血清的红细胞抗原的表达,并确定多次输血患者可能的血型表型,当无法获取血样时,还可用于检测储存的DNA。本研究评估了一种基于序列特异性引物(SSP)的血型等位基因基因分型系统,该系统适用于少量样本的快速检测,并评估了储存全血的使用情况。从20名已知ABO和Rh血型表型的献血者的新鲜血液以及储存1周和2周的血液中分离基因组DNA,并使用SSP对其进行ABO、RHD和RHCE基因分型。使用凝胶电泳和一种新型微流控芯片电泳系统对扩增子进行分析。通过SSP和凝胶电泳对新鲜血液以及储存1周和2周的血液中的DNA进行分析,所有样本均得出了正确的ABO、RHD和RHCE血型,但对于储存2周的血液中的DNA,扩增子更难可视化。使用芯片电泳SSP分析相同样本时,除了一个新鲜样本的RHCE分型出现一处差异以及一个储存2周的样本的RHCE分型出现一处差异外,所有样本的血型分型均正确。通过芯片电泳分析扩增子所需的DNA量是凝胶电泳的十分之一,并且可在30分钟内完成,而凝胶电泳则需要2小时。芯片电泳也使扩增子更易于可视化。新鲜血液以及储存1周和2周的样本均可使用SSP进行ABO和Rh基因分型。使用芯片电泳进行分析比凝胶电泳更简便、快速,但检测可靠性的变化略大。

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Microfluidic platforms for lab-on-a-chip applications.用于芯片实验室应用的微流控平台。
Lab Chip. 2007 Sep;7(9):1094-110. doi: 10.1039/b706364b. Epub 2007 Jul 27.
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Red blood cell antigen phenotype by DNA analysis.通过DNA分析确定红细胞抗原表型。
Transfusion. 2007 Jul;47(1 Suppl):60S-3S. doi: 10.1111/j.1537-2995.2007.01312.x.

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