Literature DB >> 34845695

Real-Time Detection of Viroids Using Singleplex and Multiplex Quantitative Polymerase Chain Reaction.

Fatima Osman1, Georgios Vidalakis2.   

Abstract

Multiplex quantitative polymerase chain reaction (multiplex qPCR) enables the amplification of more than one target in a single reaction using different reporter dyes with distinct fluorescent spectra. The number of reporter fluorophores is typically restricted to three or four, depending upon the capability of the real-time PCR platform and software used. Each target is amplified by a different set of primers and a uniquely labeled probe that distinguishes each PCR amplicon. Thus, the levels of several targets of interest can be quantified in real time. By combining several reactions in a single tube, multiplex qPCR reduces the quantity, and cost of reagents needed to screen a sample for multiple targets. Specificity and efficiency are not affected by the inclusion of the three assays in a multiplex reaction.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Fluorescence; Hydrolysis probes; MIQE; Minor groove binding; dsDNA intercalating molecules

Mesh:

Substances:

Year:  2022        PMID: 34845695     DOI: 10.1007/978-1-0716-1464-8_16

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Full genome characterization of 12 citrus tatter leaf virus isolates for the development of a detection assay.

Authors:  Shih-Hua Tan; Fatima Osman; Sohrab Bodaghi; Tyler Dang; Greg Greer; Amy Huang; Sarah Hammado; Shurooq Abu-Hajar; Roya Campos; Georgios Vidalakis
Journal:  PLoS One       Date:  2019-10-17       Impact factor: 3.240

  1 in total

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