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Capillary electrophoresis for capture and concentrating of target nucleic acids by affinity gels modified to contain single-stranded nucleic acid probes

机译:毛细管电泳,用于通过修饰为包含单链核酸探针的亲和凝胶来捕获和浓缩目标核酸

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摘要

Selective capture and pre-concentration of target nucleic acids from relatively complicated samples may provide a method to facilitate introduction to a microfluidic-based detection system to improve detection limits. An acrylamide polymer gel modified with Acrydite (TM) that contained 20mer oligonucleotide probe was prepared and loaded into a capillary column. The results indicated that the amount of probe DNA that was captured into the acrylamide was about 40% of the starting monomer, and different quantities of probe could therefore be coupled into the gel. The gel was passivated by pre-treatment with non-complementary DNA oligonucleotide to block non-selective adsorption sites, and the gel was determined to be stable for multiple cycles of use. The probe could hybridize with target sequences that were introduced by electrokinetic injection from a sample solution. The target could be freed from the polymer gel by use of a combination of heating, chaotropic salt and voltage conditions. Target capture efficiency was up to 90% when using samples that did not saturate probe sites in the columns, and recovery of target from the gel could be as high as 95%. (c) 2006 Elsevier B.V. All rights reserved.
机译:从相对复杂的样品中选择性捕获和预富集目标核酸可以提供一种方法,以利于引入基于微流体的检测系统以提高检测限。制备了含有20mer寡核苷酸探针的用Acrydite TM改性的丙烯酰胺聚合物凝胶,并将其装载到毛细管柱中。结果表明,捕获到丙烯酰胺中的探针DNA量约为起始单体的40%,因此可以将不同数量的探针偶联到凝胶中。通过用非互补DNA寡核苷酸预处理来钝化该凝胶以封闭非选择性吸附位点,并且确定该凝胶对于多次使用循环是稳定的。该探针可以与通过电动注射从样品溶液中引入的靶序列杂交。通过加热,离液盐和电压条件的组合,可以从聚合物凝胶中释放出靶标。当使用未使柱中探针位点饱和的样品时,目标捕获效率高达90%,并且从凝胶中回收的目标物可能高达95%。 (c)2006 Elsevier B.V.保留所有权利。

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