首页> 外文会议>NSTI Nanotechnology Conference and Trade Show(NSTI Nanotech 2005) vol.1; 20050508-12; Anaheim,CA(US) >Purification of PCR-Inhibitory Components by Cellulose Acetate Membranes
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Purification of PCR-Inhibitory Components by Cellulose Acetate Membranes

机译:醋酸纤维素膜纯化PCR抑制成分

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Conventional methods for extracting DNA from blood results in the presence of heme, which is an inhibitory factor decreasing PCR sensitivity. Current techniques for removing the inhibitors are laborious, costly, and/or sample-specific. We investigated using electrophoresis and a biopolymer membrane to separate DNA from heme. These membranes are biocompatible, can be cast directly onto silicon wafers using a standard microfabrication process without use of adhesives or introduction of exogenous contaminants. We have characterized the membranes' properties and altered their casting conditions yielding a filter with a low molecular weight cut-off: 350Da. Purified genomic DNA was mixed with hemoglobin, and the mixture was boiled to denature the DNA and dissociate the hemoglobin releasing heme into solution. The solution was immediately cooled, and placed in a chamber on one side of the membrane. By applying an electric field across this membrane, and running the experiment on ice, we were able to pass the single-stranded DNA while restricting heme since its formula weight (614Da) is larger than the membrane cutoff. The DNA was purified and enriched as observed by spectrophotometry. These membranes are easy to make, inexpensive, and can be incorporated into existing DNA chips, thereby adding a purification module to create a lab-on-a-chip design.
机译:从血液中提取DNA的常规方法会导致血红素的存在,而血红素是抑制PCR敏感性的抑制因子。当前去除抑制剂的技术是费力的,昂贵的和/或样品特异性的。我们研究了使用电泳和生物聚合物膜从血红素中分离DNA。这些膜具有生物相容性,可以使用标准的微细加工工艺直接浇铸到硅片上,而无需使用粘合剂或引入外来污染物。我们已经对膜的特性进行了表征,并改变了其浇铸条件,从而生产出截留分子量低至350Da的过滤器。将纯化的基因组DNA与血红蛋白混合,并将混合物煮沸以使DNA变性并使血红蛋白解离,从而将血红素释放到溶液中。立即将溶液冷却,并置于膜一侧的腔室中。通过在该膜上施加电场,并在冰上进行实验,我们能够通过单链DNA并限制血红素,因为它的分子式重量(614Da)比膜截止值大。如通过分光光度法观察到的,纯化并富集DNA。这些膜易于制造,价格低廉,并且可以结合到现有的DNA芯片中,从而增加了纯化模块以创建芯片实验室设计。

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