Abstract
The critical aspects of successful in situ amplification include fixation, permeabilization, amplification and detection. We address these aspects and present a novel detection scheme that eliminates hybridization following amplification. We use the 5'-nuclease activity of Tag polymerase to cleave in situ a 5'-reporter dye from an oligonucleotide probe which hybridizes to the target amplicon during amplification. The 5'-reporter dye is disassociated from the 3'-quenching dye and remains localized by charge interactions. In addition, we describe probe design constraints for 5'-nuclease assays both in solution and in situ. Using this technique, we show the sensitive and specific detection of HIV-1 DNA in cells lines and tissue from HIV-1-infected individuals.
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CITATION STYLE
Patierson, B. K., Jiyamapa, D., Mayrand, E., Hoff, B., Abramson, R., & Garcia, P. M. (1996). Detection of HIV-1 DNA in cells and tissue by fluorescent in situ 5’-nuclease assay (FISNA). Nucleic Acids Research, 24(18), 3656–3658. https://doi.org/10.1093/nar/24.18.3656
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