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新型荧光氰基核苷酸的比较研究:利用生物芯片对标记 PCR 产物进行杂交分析。

Comparative Study of Novel Fluorescent Cyanine Nucleotides: Hybridization Analysis of Labeled PCR Products Using a Biochip.

机构信息

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991, Moscow, Russia.

出版信息

J Fluoresc. 2017 Nov;27(6):2001-2016. doi: 10.1007/s10895-017-2139-6. Epub 2017 Jul 28.

Abstract

This study investigated the synthesis and substrate properties of Cy5-labeled dUTP derivatives with different substituents, linkers between the dye unit and pyrimidine heterocycle and fluorophore charges. Fluorescently labeled nucleoside triphosphates were studied as substrates using multiplex PCR with Taq and Vent (exo-) DNA polymerases, the typical representatives of the A and B polymerase families. The efficiency of nucleotide incorporation during PCR was assessed with a multi-parameter hybridization analysis using a diagnostic DNA microarray. The hybridization analysis indirectly estimates the incorporation efficiency of dye-labeled nucleotides in multiplex PCR. Our results demonstrated higher efficiencies of substrates with electrically neutral dyes than electropositive and electronegative Cy5 residues.

摘要

本研究探讨了具有不同取代基、染料单元和嘧啶杂环之间连接体以及荧光团电荷的 Cy5 标记 dUTP 衍生物的合成和底物特性。使用 Taq 和 Vent(外切)DNA 聚合酶(A 和 B 聚合酶家族的典型代表)的多重 PCR 研究了荧光标记的核苷三磷酸作为底物。使用诊断 DNA 微阵列的多参数杂交分析评估 PCR 过程中核苷酸掺入的效率。杂交分析间接估计了多聚酶链反应中染料标记核苷酸的掺入效率。我们的结果表明,带负电荷和带正电荷的 Cy5 残基比电中性染料的底物具有更高的效率。

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