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利用聚合酶链反应和随机寡核苷酸引物进行特异性DNA扩增:应用于抗原受体可变区的分析。

Specific DNA amplification utilizing the polymerase chain reaction and random oligonucleotide primers: application to the analysis of antigen receptor variable regions.

作者信息

Williams W V, Sato A, Rossman M, Fang Q, Weiner D B

机构信息

Rheumatology Section, University of Pennsylvania School of Medicine, Philadelphia 19104.

出版信息

DNA Cell Biol. 1992 Nov;11(9):707-20. doi: 10.1089/dna.1992.11.707.

Abstract

The polymerase chain reaction (PCR) allows rapid amplification of DNA of known sequence. In many situations, part of a genetic sequence is known, but adjacent sequences of interest are unknown. This is common in investigations of antigen receptor genes from B and T lymphocytes, which are composed of a constant region of known sequence and a variable region, for which the sequence may not be known. Herein is described a method to amplify DNA when sequence information is available for only one primer. This procedure utilizes a primer of known sequence in conjunction with a mixture of short random primers. Application of this method to the amplification of T-cell antigen receptor cDNA is described.

摘要

聚合酶链反应(PCR)可实现对已知序列DNA的快速扩增。在许多情况下,部分基因序列已知,但感兴趣的相邻序列未知。这在对B和T淋巴细胞抗原受体基因的研究中很常见,这些基因由已知序列的恒定区和序列可能未知的可变区组成。本文描述了一种在仅一个引物具有序列信息时扩增DNA的方法。该方法使用已知序列的引物与短随机引物混合物相结合。本文还描述了该方法在T细胞抗原受体cDNA扩增中的应用。

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