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一种用于PCR样品芯片分析的简单灵敏的瞬态免疫血小板减少症方法。 (注:这里原文的ITP可能存在错误,推测正确的是免疫血小板减少症相关的免疫检测方法Immuno-Thrombocytopenia之类的,按照字面翻译就是这样结果,但从专业角度看这个表述不太准确,可能原文有误。)

A simple and sensitive transient ITP method for on-chip analysis of PCR samples.

作者信息

Wang Lihui, Liu Dayu, Chen Hao, Zhou Xiaomian

机构信息

Department of Pathology, Dalian Medical University, Dalian, PR China.

出版信息

Electrophoresis. 2008 Dec;29(24):4976-83. doi: 10.1002/elps.200800258.

Abstract

We present a sensitive, simple and robust on-chip transient ITP (TITP) method for the analysis of polymerase chain reaction (PCR) samples. This TITP analysis was performed on a poly (methyl methacrylate) microchip with cross structure. The PCR sample was injected into a 4 mm free-solution buffer channel to increase sample loading. When applied separation voltage, the sample ions were stacked by TITP using chloride ions in the sample matrix as the leading ions and HEPES in the background electrolyte as the terminating ions. The stacked sample plug was then separated by zone electrophoresis (ZE) in hydroxypropylmethyl cellulose polymer. The whole operation was carried out in single background electrolyte. Sample injection, preconcentration / separation were performed continuously with the sequential switching of voltage. By injection of the sample into the free-solution buffer channel, sampling bias was avoided and the injection time was reduced. With this TITP method, the detection sensitivity was improved without loss of resolution, a 20-fold signal enhancement was achieved and the average limit of detection was estimated to be 0.24 pg/microL (S/N = 3). The TITP method is simple, fast and sensitive, thus is well suited to direct analysis of the highly saline PCR samples.

摘要

我们提出了一种灵敏、简单且稳健的芯片上瞬态等速电泳(TITP)方法,用于分析聚合酶链反应(PCR)样品。该TITP分析在具有交叉结构的聚甲基丙烯酸甲酯微芯片上进行。将PCR样品注入4毫米的自由溶液缓冲通道以增加样品加载量。施加分离电压时,使用样品基质中的氯离子作为前导离子,背景电解质中的HEPES作为终止离子,通过TITP使样品离子堆积。然后,堆积的样品塞在羟丙基甲基纤维素聚合物中通过区带电泳(ZE)进行分离。整个操作在单一背景电解质中进行。通过顺序切换电压连续进行样品注入、预浓缩/分离。通过将样品注入自由溶液缓冲通道,避免了进样偏差并减少了进样时间。使用这种TITP方法,在不损失分辨率的情况下提高了检测灵敏度,实现了20倍的信号增强,估计平均检测限为0.24 pg/微升(S/N = 3)。TITP方法简单、快速且灵敏,因此非常适合直接分析高盐度的PCR样品。

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