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首页> 外文期刊>Tissue antigens. >Oligonucleotide microarray for HLA-DRB1 genotyping: preparation and clinical evaluation.
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Oligonucleotide microarray for HLA-DRB1 genotyping: preparation and clinical evaluation.

机译:用于HLA-DRB1基因分型的寡核苷酸微阵列:制备和临床评估。

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摘要

In this study, HLA-DRB1 gene was genotyped by using the microarray technique. Oligonucleotide probes were designed based on partial sequences of various genotypes of HLA-DRB1, and were fixed on a silylated slide to form a microarray. The second exon of HLA-DRB1 gene in the extracted genomic DNA samples was amplified and labelled by means of polymerase chain reaction (PCR); then it was hybridized to the microarray. The microarray was scanned, and the result was analysed in order to determine the genotypes of HLA-DRB1 of the tested sample. A total of 1574 of 1592 clinical samples had accordant results of genotypes in either microarray assay or PCR-SSP assay; 8 of 10 samples that had inconsistent results of genotypes were proved to be microarray-assay reliable by confirmation of DNA sequencing. It is concluded that microarray is an alternative reliable method for HLA-DRB1 genotyping.
机译:在这项研究中,通过使用微阵列技术对HLA-DRB1基因进行了基因分型。基于HLA-DRB1的各种基因型的部分序列设计寡核苷酸探针,并将其固定在甲硅烷基化的载玻片上以形成微阵列。提取的基因组DNA样品中HLA-DRB1基因的第二个外显子通过聚合酶链反应(PCR)进行扩增和标记;然后将其与微阵列杂交。扫描微阵列,并对结果进行分析,以确定被测样品的HLA-DRB1基因型。在微阵列测定或PCR-SSP测定中,共有1592份临床样本中的1574份具有相同的基因型结果;基因序列结果不一致的10个样品中有8个通过确认DNA测序被证明是微阵列分析可靠的。结论是,微阵列是HLA-DRB1基因分型的另一种可靠方法。

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