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用于基于微芯片的双链DNA毛细管电泳的聚合物基质设计。

Designing polymer matrix for microchip-based double-stranded DNA capillary electrophoresis.

作者信息

Zhang Jun, He Weidong, Liang Dehai, Fang Dufei, Chu Benjamin, Gassmann Marcus

机构信息

Department of Chemistry, Stony Brook University, Stony Brook, NY 11794-3400, USA.

出版信息

J Chromatogr A. 2006 Jun 9;1117(2):219-27. doi: 10.1016/j.chroma.2006.03.106. Epub 2006 Apr 19.

Abstract

Polyacrylamide (PAM) was used as a model polymer to build up an empirical model that relates polymer molecular weight, polymer concentration and solution viscosity. The desired random copolymers of acrylamide (AM) and N,N-dimethylacrylamide (DMA) used as DNA separation media for different specifications were synthesized under the guidance of the empirical model. The separation performances of rationally designed copolymers were tested in a 1.2 cm long separation channel, simulating microchip-based capillary electrophoresis. pBR322/HaeIII digest was successfully separated with good separation resolution and fast speed. Validation of the sieving ability of our polymers was performed in the Agilent 2,100 Bioanalyzer. The results of the 10 bp (base pair) DNA ladder separation demonstrate the potential of our approach for the sieving matrix in microchip-based electrophoresis.

摘要

聚丙烯酰胺(PAM)被用作模型聚合物来建立一个经验模型,该模型将聚合物分子量、聚合物浓度和溶液粘度联系起来。在该经验模型的指导下,合成了用于不同规格DNA分离介质的所需丙烯酰胺(AM)和N,N - 二甲基丙烯酰胺(DMA)的无规共聚物。在一个1.2厘米长的分离通道中测试了合理设计的共聚物的分离性能,模拟基于微芯片的毛细管电泳。pBR322/HaeIII酶切片段成功分离,分离分辨率良好且速度快。在安捷伦2100生物分析仪中对我们的聚合物的筛分能力进行了验证。10 bp(碱基对)DNA阶梯分离的结果证明了我们的方法在基于微芯片的电泳中作为筛分基质的潜力。

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