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

机译:用于定量低于100分子/ ml的核酸靶标的分支DNA信号扩增测定法。

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摘要

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 signaloise 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.
机译:通过在扩增序列中包含新型核苷酸isoC和isoG可以防止非特异性杂交,从而改进了分支DNA杂交检测。新型的含isoC,isoG的扩增序列与任何天然DNA序列均未检测到相互作用。非特异性杂交的控制又允许增加信号放大。发现增加一个14位的前置放大器会使信噪比增加8倍。针对共有的HIV POL序列设计了74个寡核苷酸探针。这种新的HIV支链DNA扩增子测定的检测限约为50个分子/ ml。该测定法用于在三重药物疗法中测量87例HIV感染患者的血浆样本中的病毒载量,其RNA效价<500分子/ ml。在所有11位患者中,病毒载量最终均下降至新检测法的检测极限以下。

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