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用于使用毛细管阵列电泳进行非变性DNA分离的通用低粘度筛分基质。

Versatile low-viscosity sieving matrices for nondenaturing DNA separations using capillary array electrophoresis.

作者信息

Madabhushi R S, Vainer M, Dolnik V, Enad S, Barker D L, Harris D W, Mansfield E S

机构信息

Molecular Dynamics, Inc., Sunnyvale, CA 94086, USA.

出版信息

Electrophoresis. 1997 Jan;18(1):104-11. doi: 10.1002/elps.1150180120.

Abstract

The high-resolution separation of double-stranded DNA (dsDNA) has important applications in physical mapping strategies and in the analysis of polymerase chain reaction (PCR) products. Although high-resolution separations of dsDNA by capillary electrophoresis (CE) have been reported, pulsed fields were required to achieve complete resolution of DNA fragments beyond 23 kilobase pairs (kbp). Here, we report a single formulation to separate a broad range (80 bp-40 kbp) of DNA fragments without the use of pulsed fields. We used a low-viscosity sieving medium (ca. 5 cP, at 25 degrees C) based on polyethyleneoxide (PEO) to separate DNA fragments up to 40 kbp. The matrix contained a mixture of 0.5% PEO (Mn 10(6)) to separate fragments up to 1.5 kbp, combined with 0.1% PEO (Mn 8 x 10(6)) to separate fragments between 1-40 kbp, within a single run. All PEO matrix formulations tested were compatible with a variety of intercalating dyes and with two different capillary wall coating methods. We obtained a detection limit of 25 fg of a 200 bp DNA quantitation standard using Vistra Green in the matrix. Resolution was best using short injection times (5 s or less) and low field strengths (approximately 100 V/cm). Sample runs were complete in 70 min, and use of the capillary array electrophoresis (CAE) system permitted high-throughput DNA analysis. The size range separated is approximately 10 times greater than with conventional slab gel separations.

摘要

双链DNA(dsDNA)的高分辨率分离在物理图谱策略和聚合酶链反应(PCR)产物分析中具有重要应用。尽管已有通过毛细管电泳(CE)对dsDNA进行高分辨率分离的报道,但对于超过23千碱基对(kbp)的DNA片段,需要使用脉冲场才能实现完全分离。在此,我们报道了一种单一配方,可在不使用脉冲场的情况下分离宽范围(80 bp - 40 kbp)的DNA片段。我们使用基于聚环氧乙烷(PEO)的低粘度筛分介质(25℃时约5 cP)来分离长达40 kbp的DNA片段。该基质包含0.5% PEO(Mn 10⁶)的混合物以分离长达1.5 kbp的片段,并与0.1% PEO(Mn 8 x 10⁶)结合以在单次运行中分离1 - 40 kbp之间的片段。所有测试的PEO基质配方都与多种嵌入染料以及两种不同的毛细管内壁涂层方法兼容。我们使用基质中的Vistra Green对200 bp DNA定量标准品获得了25 fg的检测限。使用短进样时间(5秒或更短)和低场强(约100 V/cm)时分辨率最佳。样品运行在70分钟内完成,并且使用毛细管阵列电泳(CAE)系统可实现高通量DNA分析。分离的大小范围比传统平板凝胶分离大约大10倍。

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