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通过体外扩增对核酸进行扫描:新进展与应用

Scanning of nucleic acids by in vitro amplification: new developments and applications.

作者信息

Caetano-Anollés G

机构信息

Department of Ornamental Horticulture and Landscape Design, University of Tennessee, Knoxville 37901-1071, USA.

出版信息

Nat Biotechnol. 1996 Dec;14(13):1668-74. doi: 10.1038/nbt1296-1668.

Abstract

Nucleic acids can be characterized using a variety of "fingerprinting" techniques usually based on nucleic acid hybridization or enzymatic amplification. The scanning of nucleic acids by amplification with arbitrary oligonucleotide primers has become popular because it can generate simple-to-complex patterns from anonymous DNA or RNA templates without requiring prior knowledge of nucleic acid sequence or cloned or characterized probes. Discrete loci are amplified within genomic DNA, DNA complementary to mRNA populations (cDNA), cloned DNA fragments, and even PCR products. The potential and limitations of the various genome scanning techniques, novel improvements, and their recent use in comparative and experimental biology applications, including the analysis of plant and bacterial genomes are discussed.

摘要

核酸可以使用多种通常基于核酸杂交或酶促扩增的“指纹”技术进行表征。用任意寡核苷酸引物进行扩增来扫描核酸已变得很流行,因为它可以从无名的DNA或RNA模板生成从简单到复杂的图谱,而无需事先了解核酸序列或克隆或表征的探针。离散位点在基因组DNA、与mRNA群体互补的DNA(cDNA)、克隆的DNA片段甚至PCR产物中被扩增。讨论了各种基因组扫描技术的潜力和局限性、新的改进及其最近在比较和实验生物学应用中的使用,包括植物和细菌基因组的分析。

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