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The loop-mediated isothermal amplification (LAMP) assay for Piper yellow mottle virus and the reverse transcription (RT) LAMP assay for Cucumber mosaic virus each consisted of a set of five primers designed against the conserved sequences in the viral genome.
The sensitivity of the duplex LAMP assay for cow and goat was 0.1 and 1 pg, respectively.
This paper reports the development of a visual loop-mediated isothermal amplification (LAMP) assay for rapid detection of the pathogen.
To our knowledge this is the first report of the use of a multiplex LAMP assay for fungal organisms.
The objective of this study was to develop a new LAMP assay for the detection of Salmonella ser.
The present study was designed to develop a loop-mediated isothermal amplification (LAMP) assay for the rapid and simple detection of Mycobacterium avium subsp. paratuberculosis (MAP).
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Based on the optimized reaction conditions described above, the LAMP assays for detecting Lxx in sugarcane was established.
The unique characteristics of a phage-borne peptide that connects the peptide with affinity to a target on the phage particles containing nucleic acids (single-stranded DNA) encoding the peptide make them excellent reagents to develop LAMP assays for small molecules.
As per our knowledge and available literature, the present study reports first time about the usefulness of RT-LAMP assay for detection of CTV from India.
The objective of this study was to develop a reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for detection of type II porcine reproductive and respiratory syndrome virus (PRRSV).
The feasibility of the RT-LAMP assay for detection of IPNV RNA in clinical specimen was authenticated using kidney tissue samples from experimentally IPNV-infected Atlantic salmon (Salmo salar) post-smolts.
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