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首页> 外文期刊>Tissue antigens. >Sequence analysis of the novel allele HLA-B*070502.
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Sequence analysis of the novel allele HLA-B*070502.

机译:新型等位基因HLA-B * 070502的序列分析。

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摘要

We here describe the identification of the novel allele HLA-B*070502, which has been detected in a potential bone marrow donor. The HLA class I typing results were A*24,*29; B*070502,*5701. Initial testing at the HLA-B locus was performed by an external institute by two independent techniques -PCR-SSO (sequence-specific oligonu-cleotides) and PCR-SSP (sequence-specific primers). No match result was obtained by PCR-SSO due to the detection of one inconclusive reaction, whereas the unambiguous result HLA-B*0713 was obtained by PCR-SSP. The inconclusive reaction pattern in PCR-SSO and the detection of a rare allele in PCR-SSP suggested the presence of a new allele, which was further investigated by PCR-SBT. Cycle sequencing of exons 2 and 3 was performed following haplotype-specific amplification essentially as previously described (1) using an Applied Biosystems (Foster City, CA, USA) 3730 sequencer, resulting in the detection of the new allele.
机译:我们在此描述了在潜在的骨髓供体中已检测到的新型等位基因HLA-B * 070502的鉴定。我输入的HLA类结果为A * 24,* 29; B * 070502,* 5701。外部机构通过两项独立的技术-PCR-SSO(序列特异性寡核苷酸)和PCR-SSP(序列特异性引物)在HLA-B基因座进行了初步测试。由于检测到一个不确定的反应,通过PCR-SSO未获得匹配结果,而通过PCR-SSP获得了明确的结果HLA-B * 0713。 PCR-SSO中不确定的反应模式和PCR-SSP中稀有等位基因的检测表明存在新的等位基因,PCR-SBT对其进行了进一步研究。基本如先前所述(1),使用Applied Biosystems(Foster City,CA,USA)3730测序仪进行单倍型特异性扩增后,对外显子2和3进行循环测序,从而检测到新的等位基因。

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