Quantitative Reverse Transcription Strand Displacement Amplification: Quantitation of Nucleic Acids Using an Isothermal Amplification Technique

1998 ◽  
Vol 259 (2) ◽  
pp. 226-234 ◽  
Author(s):  
Colleen M. Nycz ◽  
Cheryl H. Dean ◽  
Perry D. Haaland ◽  
Catherine A. Spargo ◽  
G.Terrance Walker
Sensors ◽  
2021 ◽  
Vol 21 (2) ◽  
pp. 602
Author(s):  
Sandra Leonardo ◽  
Anna Toldrà ◽  
Mònica Campàs

The easy and rapid spread of bacterial contamination and the risk it poses to human health makes evident the need for analytical methods alternative to conventional time-consuming laboratory-based techniques for bacterial detection. To tackle this demand, biosensors based on isothermal DNA amplification methods have emerged, which avoid the need for thermal cycling, thus facilitating their integration into small and low-cost devices for in situ monitoring. This review focuses on the breakthroughs made on biosensors based on isothermal amplification methods for the detection of bacteria in the field of food safety and environmental monitoring. Optical and electrochemical biosensors based on loop mediated isothermal amplification (LAMP), rolling circle amplification (RCA), recombinase polymerase amplification (RPA), helicase dependent amplification (HDA), strand displacement amplification (SDA), and isothermal strand displacement polymerisation (ISDPR) are described, and an overview of their current advantages and limitations is provided. Although further efforts are required to harness the potential of these emerging analytical techniques, the coalescence of the different isothermal amplification techniques with the wide variety of biosensing detection strategies provides multiple possibilities for the efficient detection of bacteria far beyond the laboratory bench.


1992 ◽  
Vol 20 (7) ◽  
pp. 1691-1696 ◽  
Author(s):  
G. Terrance Walker ◽  
Melinda S. Fraiser ◽  
James L. Schram ◽  
Michael C. Little ◽  
James G. Nadeau ◽  
...  

2021 ◽  
Vol 1 (19) ◽  
pp. 244-246
Author(s):  
O.L. Bodulev ◽  
A.M. Soloviev

This work will present the results of the development of two new highly sensitive heterogeneous methods for the determination of miRNA-141 and miRNA-39 using the isothermal circular strand-displacement amplification and the catalytic hairpin assembly methods for analyte amplification.


1999 ◽  
Vol 276 (2) ◽  
pp. 177-187 ◽  
Author(s):  
James G. Nadeau ◽  
J.Bruce Pitner ◽  
C.Preston Linn ◽  
James L. Schram ◽  
Cheryl H. Dean ◽  
...  

2018 ◽  
Vol 9 (11) ◽  
pp. 3050-3055 ◽  
Author(s):  
Wanghua Wu ◽  
Tao Zhang ◽  
Da Han ◽  
Hongliang Fan ◽  
Guizhi Zhu ◽  
...  

A programmable sequence-specific aligner-mediated cleavage endows strand displacement amplification with excellent universality, high sensitivity, high specificity and simple primer design.


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