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作 者:陶苏丹[1] 和艳敏[1] 章伟[1] 王炜[1] 何吉[1] 朱发明[1] 吕杭军[1]
机构地区:[1]浙江省血液中心,卫生部血液安全研究重点实验室,杭州310006
出 处:《中华医学遗传学杂志》2014年第3期383-387,共5页Chinese Journal of Medical Genetics
基 金:浙江省医药卫生科学研究基金(2012KYA061,2013RCB003)
摘 要:目的建立生物素标记探针和链亲和素磁珠分离人类白细胞抗原(humanleukocyteantigen,HLA)-A、-B、-C单体型的技术,以解决HLA分型过程中部分模棱两可的结果。方法根据IMGT/HLA数据库中HLA等位基因的序列信息,设计5’端生物素标记探针。将探针与104份标本基因组DNA混合杂交,然后加入链亲和素磁珠孵育,形成链亲和素磁珠一生物素探针一单链DNA复合物,通过洗涤和解析从而实施有效的分离。对分离出的单体型基因组DNA进行HLA-A、-B或-C位点扩增和测序分析。结果设计的12个HLA-A、19个HLA-B、13个HLA-C位点探针中,经测序证实分别有9个、9个、5个探针成功分离了单链DNA标本。结论建立的探针和磁珠分离HLAA、-B、-C单体型技术具有可行性,可以解决HLA测序分型中部分模棱两可结果,提高分型的准确性。Objective To develop a method for separating the human leukocyte antigen (HLA)-A, - B and -C haploid using biotinylated probes and streptavidin magnetic beads in order to solve ambiguous HLA genotyping results. Methods Based on sequence information of HLA alleles from the IMGT/HLA database, the 5'-biotinylated probes were designed. The probe was mixed and extended with corresponding genomic DNA, and incubated with streptavidin magnetic beads, which could form a streptavidin magnetic beads-biotin-probe-DNA complex. The unique DNA haploid binding to corresponding probe was isolated after washes and elution. The separated haploid genomic DNA was used as template for HLA-A, -B and -C loci amplification and sequencing analysis. Results Among the 12 HLA-A probes, 19 HLA-B probes and 13 HLA-C probes, DNA sequencing has confirmed that 9 HLA-A probes, 9 HLA-B probes and 5 HLA-C probes could successfully separate the haploid from genomic DNA samples. Conclusion The developed method for HLA-A, -B and -C haploid separation is reliable, which can solve certain ambiguity and improve the accuracy of HLA genotyping.
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