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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Dielectrophoretic isolation and detection of cancer-related circulating cell-free DNA biomarkers from blood and plasma
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Dielectrophoretic isolation and detection of cancer-related circulating cell-free DNA biomarkers from blood and plasma

机译:血液和等离子体中癌癌无循环无细胞DNA生物标志物的介电泳分离及检测

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Conventional methods for the isolation of cancer-related circulating cell-free (ccf) DNA from patient blood (plasma) are time consuming and laborious. A DEP approach utilizing a microarray device now allows rapid isolation of ccf-DNA directly from a small volume of unprocessed blood. In this study, the DEP device is used to compare the ccf-DNA isolated directly from whole blood and plasma from 11 chronic lymphocytic leukemia (CLL) patients and one normal individual. Ccf-DNA from both blood and plasma samples was separated into DEP high-field regions, after which cells (blood), proteins, and other biomolecules were removed by a fluidic wash. The concentrated ccf-DNA was detected on-chip by fluorescence, and then eluted for PCR and DNA sequencing. The complete process from blood to PCR required less than 10 min; an additional 15 min was required to obtain plasma from whole blood. Ccf-DNA from the equivalent of 5 μL of CLL blood and 5 μL of plasma was amplified by PCR using Ig heavy-chain variable (IGHV) specific primers to identify the unique IGHV gene expressed by the leukemic B-cell clone. The PCR and DNA sequencing results obtained by DEP from all 11 CLL blood samples and from 8 of the 11 CLL plasma samples were exactly comparable to the DNA sequencing results obtained from genomic DNA isolated from CLL patient leukemic B cells (gold standard).
机译:用于与癌症相关的循环无细胞(CCF)从患者血液(血浆)DNA的分离的常规方法是耗时且费力的。利用微阵列装置中的DEP的方法现在允许直接从血液未处理小体积CCF-DNA的快速分离。在这项研究中,DEP装置被用来比较CCF-DNA直接从全血和血浆中分离出从11慢性淋巴细胞性白血病(CLL)的患者和一个正常个体。从血液和血浆样品CCF-DNA分离成DEP高场区域,在这之后的细胞(血),蛋白质和其它生物分子是由一个流体洗涤除去。通过荧光片上检测到浓缩的CCF-DNA,然后洗脱PCR和DNA测序。从血液到PCR的完整过程需要的时间少于10分钟;物需要额外的15分钟,以从全血中获得等离子体。从5μL的CLL血液和血浆的5μL的等效CCF-DNA通过PCR,使用Ig重链可变(IGHV)特异性引物以识别由白血病B细胞克隆中表达的独特IGHV基因扩增。从所有11个CLL血样并从8 11个CLL血浆样品通过DEP获得的PCR和DNA测序结果完全可比于来自CLL患者的白血病B细胞(黄金标准)分离的基因组DNA得到的DNA测序结果。

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