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一种用于检测葡萄黑痘病和葡萄黄化病植原体的实时PCR检测系统及目标DNA定量分析

A real-time PCR detection system for the bois noir and flavescence dorée phytoplasmas and quantification of the target DNA.

作者信息

Mehle Nataša, Prezelj Nina, Hren Matjaž, Boben Jana, Gruden Kristina, Ravnikar Maja, Dermastia Marina

机构信息

ational Institute of Biology, Ljubljana, Slovenia.

出版信息

Methods Mol Biol. 2013;938:253-68. doi: 10.1007/978-1-62703-089-2_22.

Abstract

The real-time PCR detection system for grapevine yellows phytoplasmas described here is composed of two assays for group-specific detection of flavescence dorée (FD) and bois noir (BN) phytoplasmas and a universal phytoplasma assay. It uses hydrolysis minor groove binder probes (TaqMan-MGB). The addition of an assay for amplification of plant DNA co-extracted with phytoplasma DNA provides a further quality control for the DNA extraction and PCR amplification for each sample. The detection system described is reliable, specific, sensitive, and easily applicable to fast, high-throughput diagnosis of grapevine yellows phytoplasmas. In addition to the detection system, an approach for the quantification of phytoplasmas in the sample is described.

摘要

本文所述的葡萄黄化植原体实时荧光定量PCR检测系统由用于特异性检测金黄萎病(FD)和黑木病(BN)植原体的两种检测方法以及一种通用植原体检测方法组成。它使用水解小沟结合探针(TaqMan-MGB)。针对与植原体DNA共提取的植物DNA进行扩增的检测方法,为每个样品的DNA提取和PCR扩增提供了进一步的质量控制。所描述的检测系统可靠、特异、灵敏,且易于应用于葡萄黄化植原体的快速、高通量诊断。除了该检测系统外,还描述了一种对样品中植原体进行定量的方法。

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