Author: Ahmed FA, Larrea-Sarmiento A, Alvarez AM, Arif M.
Recombinase polymerase amplification (RPA) combined with a lateral flow device (LFD) was developed for specific detection of Pectobacterium sp. directly from infected plant materials with no need for DNA isolation. The specificity of RPA-LFD was tested with 26 Pectobacterium sp. …
Author: Sun N, Wang W, Wang J, Yao X, Chen F, Li X, Yinglei Y, Chen B.
Three reverse transcription recombinase polymerase amplification assays with lateral flow dipsticks (RT-RPA-LFD) were developed for identification of the matrix and hemagglutinin (HA) genes to detect influenza A virus and distinguish subtypes H1 and H3. The sensitivity of RT-RPA-LFD assays is …
Author: Hou P, Zhao G, Wang H, He C, He H.
The aim of this study was to develop a novel isothermal recombinase polymerase amplification (RPA) method combined with a lateral flow dipstick (LFD), for rapid detection of BVDV. The detection limit of this assay was 20 copies per reaction, and …
Author: JianHu P, LongLiang Q, HaiLong H, ChenYang D, Peng Z, JiLin X.
In this study, several pairs of primers and an exo-probe targeting the zinc metalloprotease gene (empA) of Listonella anguillarum was designed and a rapid real-time detection method for Listonella anguillarum based on recombinase polymerase amplification (RPA) was established by optimizing …
Author: Xu J, Wang X, Yang L, Kan B, Lu X.
RPA detection based on the mcr-1 gene was successfully applied in our study. The plasmid-mediated mcr-1 gene conferring colistin drug resistance has a strong ability to spread, suggesting the need to further strengthen the detection of this resistance gene in …
Author: Li J, Wang C, Yu X, Lin H, Hui C, Shuai L, Zhang S.
Cyanobacteria are one of the major groups of algae causing algal blooms. In this study a rapid method for detecting Cyanobacteria was developed using a recombinase polymerase amplification (RPA) method coupled with lateral flow (LF) strips. The method developed in …
Author: Feng XY, Shen LB, Wang WZ, Wang JG, Cao ZY, Zhang SZ.
In this study, a novel isothermal assay was established on the basis of reverse transcription–recombinase polymerase amplification (RT-RPA) and evaluated in terms of its ability to detect SCSMV. Overall, the RT-RPA assay was specific, sensitive, reliable, and rapid for SCSMV …
Author: Burkhardt A, Henry PM, Koike ST,Gordon T, Martin FN.
In this study, next-generation sequencing and comparative genomics were used to identify a unique genetic locus that can detect all the somatic compatibility groups of F. oxysporum f. sp. fragariae identified in California. This locus was used to develop a …
Author: Subbotin SA.
RPA assays were developed targeting the IGS rRNA gene of the pacara earpod tree root-knot nematode, Meloidogyne enterolobii. The RPA assays using TwistAmp® Basic and TwistAmp® exo kits allowed detection of M. enterolobii from gall tissues and crude nematode extracts …
Author: Liu MZ, Han XH, Yao LQ, Zhang WK, Liu BS, Chen ZL.
A recombinase polymerase amplification (RPA) assay (RPA-LFD-FHV) combined with a lateral flow dipstrip (LFD) was developed that uses human body heat for incubation. The RPA-FLD-FHV assay is a simple, rapid, and reliable method for point-of-care diagnosis of FHV-1 infection.
Dear Valued Clients and Partners,
We are pleased to inform you that our office will be moving to the following new address effective September 08th 2021.
New address:
Biolinkk
Third Floor, Plot No. 25, Block-B, Community Centre, Janakpuri, New Delhi- 110058 (India)
We apologize for any inconvenience that you may encounter during our move dates. Should you have any questions on the relocation, please feel free to contact us.
Look forward to seeing and serving you at our new facility.
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