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

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Collins, M.·1997·Nucleic Acids Research

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.

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Metadata

Authors
Collins, M.
Venue
Nucleic Acids Research
Published
1997-08-01
Volume
25
Issue
15
Pages
2979-2984
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2120064644
Cited by
317
References
0
FWCI
5.40
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml. https://app.cochat.ai/papers/10.1093/nar/25.15.2979
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Collins, M. (1997). A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml. Nucleic Acids Research. https://doi.org/10.1093/nar/25.15.2979

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