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首页> 外文期刊>BioTechniques >Improved multiple displacement amplification with varphi29 DNA polymerase for genotyping of single human cells.
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Improved multiple displacement amplification with varphi29 DNA polymerase for genotyping of single human cells.

机译:使用varphi29 DNA聚合酶改进的多置换扩增,用于单个人细胞的基因分型。

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摘要

The ability to genotype multiple loci of single cells would be of significant benefit to investigations of cellular processes such as oncogenesis, meiosis, fertilization, and embryogenesis. We report a simple two-step, single-tube protocol for whole-genome amplification (WGA) from single human cells using components of the GenomiPhi V2 DNA Amplification kit. For the first time, we demonstrate reliable generation of 4-7 microg amplified DNA from a single human cell within 4 h with a minimum amount of artifactual DNA synthesis. DNA amplified from single cells was genotyped for 13 heterozygous short tandem repeats (STRs) and 7 heterozygous single nucleotide polymorphisms (SNPs), and the genotyping results were compared with purified genomic DNA. Accuracy of genotyping (percent of single-cell amplifications genotyped accurately for any particular STR or SNP) varied from 37% to 100% (with an average of 80%) for STRs and from 89% to 100% (averaging 94%) for SNPs. We suggest that the method described in this report is suitable for WGA from single cells, the product of which can be subsequently used for many applications, such as preimplantation genetic analysis (PGD).
机译:对单个细胞的多个基因座进行基因分型的能力将对研究诸如癌发生,减数分裂,受精和胚胎发生等细胞过程具有重大益处。我们报告了一个简单的两步,单管协议,使用GenomiPhi V2 DNA扩增试剂盒的成分从单个人细胞进行全基因组扩增(WGA)。首次,我们证明了在4小时内从单个人类细胞可靠生成4-7微克扩增的DNA,并且人工合成的DNA量最少。从单细胞扩增的DNA进行了13个杂合的短串联重复序列(STR)和7个杂合的单核苷酸多态性(SNP)的基因分型,并将基因分型结果与纯化的基因组DNA进行了比较。基因分型的准确性(对于任何特定的STR或SNP,准确进行基因分型的单细胞扩增的百分比)对于STRs,从37%到100%(平均为80%),对于SNPs,从89%到100%(平均为94%)。 。我们建议本报告中描述的方法适用于单细胞WGA,其产物可随后用于许多应用,例如植入前遗传分析(PGD)。

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