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STR loci analysis of buccal cavity cells captured by laser microdissection

机译:激光微粉捕获的颊腔电池的STR基因座分析

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We intended to analyze short tandem repeat (STR) loci in low copy-numbei DNA from buccal cavity cells The cell smears were stained with Hanis' hematoxylin and eosin for the STR analysis Individual cells were captured by laser microdissection using a PALM Microlaser System After the whole genome was amplified using the improved primer extension pie-amplification PCR (I-PEP-PCR) metho,15 loci, D8S1179, D21S11, D7S820, CSF1PO, D3S1358, TH01, D13S317, D16S539, D2S1339, D19S433, vWA, TPOX, D18S51, D5S818, and FG,As well as the Amelogenin locus were amplified using the AmpFISTR Identifiler PCR amplification kit. We resolved the 15 STR loci and the Amelogenin locus from 20 buccal cavity cells, 13 STR loci and the Amelogenin locus from 10 buccal cavity cells, nine STR loci and the Amelogenin locus from five buccal cavity cells, and five STR loci and the Amelogenin locus from two buccal cavity cells This is a feasible method for analyzing STR loci and the Amelogenin locus of low copy-number DNA.
机译:我们打算分析来自颊腔细胞的低拷贝Cumbei DNA中的短串联重复(str)基因座,细胞涂片用Hanis'苏木精染色,STS分析的曙红通过激光微探针捕获单个细胞在后面使用改进的引物延伸饼膨胀PCR(I-PEP-PCR)Metho,15个基因座,D8S1179,D21S11,D3S1358,CSF1PO,D3S1358,TH01,D13S317,D16S539,D2S1339,D19S433,VWA,TPOX,D18S51(D1339),D2S11,D18S51(D2S1317),D2S11,D16S433,VWA ,使用AMPFISTR识别PCR扩增试剂盒扩增D5S818和FG,以及Amelogenin轨迹。从10个颊腔电池,九个颊腔电池,九条座位和Amelogenin基因座,来自五个颊腔电池,5 str基因座和Amelogenin基因座,解决了来自20个颊腔电池,13 st基因座和Amelogenin基因座的15 stroci in和amelogenin轨迹。来自两个颊腔电池,这是分析STR基因座和低拷贝数DNA的amelogen遗迹的可行方法。

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