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使用荧光引物和GENESCAN软件分析差异显示RT-PCR产物。

Analysis of differential display RT-PCR products using fluorescent primers and GENESCAN software.

作者信息

Luehrsen K R, Marr L L, van der Knaap E, Cumberledge S

机构信息

PE Applied Biosystems, Foster City, CA, USA.

出版信息

Biotechniques. 1997 Jan;22(1):168-74. doi: 10.2144/97221pf01.

Abstract

Differential display reverse transcription PCR (DDRT-PCR) is a procedure used to identify the induction or repression of gene expression. In most DDRT-PCR protocols, radioisotopes are incorporated during PCR and the cDNA products are detected by autoradiography. This report describes the fluorescent labeling of cDNAs and their detection on automated sequencers from PE Applied Biosystems. A fluorescent tag can be incorporated into the PCR product by using either a labeled primer or a labeled dUTP. The fluorescent signals are analyzed by GENESCAN software. Fluorescent DDRT-PCR increases throughput and obviates the handling of hazardous radioisotopes. A PCR cycling profile, expected to give improved reproducibility, is also described. Because amplified cDNAs can't be recovered from the automated sequencer gel, suggestions are given for the identification and recovery of differentially expressed cDNAs.

摘要

差异显示逆转录PCR(DDRT-PCR)是一种用于鉴定基因表达的诱导或抑制的方法。在大多数DDRT-PCR方案中,在PCR过程中掺入放射性同位素,并且通过放射自显影检测cDNA产物。本报告描述了cDNA的荧光标记及其在PE应用生物系统公司的自动测序仪上的检测。可以通过使用标记引物或标记的dUTP将荧光标签掺入PCR产物中。荧光信号由GENESCAN软件分析。荧光DDRT-PCR提高了通量,避免了对有害放射性同位素的处理。还描述了一种有望提高重现性的PCR循环程序。由于无法从自动测序仪凝胶中回收扩增的cDNA,因此给出了鉴定和回收差异表达cDNA的建议。

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