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一种用于定量低于100分子/毫升核酸靶标的分支DNA信号放大检测法。

A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml.

作者信息

Collins M L, Irvine B, Tyner D, Fine E, Zayati C, Chang C, Horn T, Ahle D, Detmer J, Shen L P, Kolberg J, Bushnell S, Urdea M S, Ho D D

机构信息

Chiron Diagnostics, 4560 Horton Street, Emeryville, CA 94608, USA.

出版信息

Nucleic Acids Res. 1997 Aug 1;25(15):2979-84. doi: 10.1093/nar/25.15.2979.

Abstract

The branched DNA hybridization assay has been improved by the inclusion of the novel nucleotides, isoC and isoG, in the amplification sequences to prevent non-specific hybridization. The novel isoC, isoG-containing amplification sequences have no detectable interaction with any natural DNA sequence. The control of non-specific hybridization in turn permits increased signal amplification. Addition of a 14 site preamplifier was found to increase the signal/noise ratio 8-fold. A set of 74 oligonucleotide probes was designed to the consensus HIV POL sequence. The detection limit of this new HIV branched DNA amplifier assay was approximately 50 molecules/ml. The assay was used to measure viral load in 87 plasma samples of HIV- infected patients on triple drug therapy whose RNA titers were <500 molecules/ml. In all 11 patients viral load eventually declined to below the detection limit with the new assay.

摘要

通过在扩增序列中加入新型核苷酸异胞嘧啶(isoC)和异鸟嘌呤(isoG)来防止非特异性杂交,从而改进了分支DNA杂交检测法。含有新型isoC和isoG的扩增序列与任何天然DNA序列均无可检测到的相互作用。对非特异性杂交的控制进而允许增加信号放大。发现添加一个14位点的预扩增器可使信噪比提高8倍。针对HIV POL共有序列设计了一组74个寡核苷酸探针。这种新型HIV分支DNA扩增检测法的检测限约为50个分子/毫升。该检测法用于测量87例接受三联药物治疗且RNA滴度<500个分子/毫升的HIV感染患者的血浆样本中的病毒载量。在所有11例患者中,使用新检测法最终病毒载量均降至检测限以下。

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