Results 261 to 270 of about 494,714 (299)

Assessment of reference genes for qRT-PCR normalization to elucidate host response to African swine fever infection. [PDF]

open access: yesBraz J Microbiol
Rajkhowa S   +8 more
europepmc   +1 more source

Comparative Analysis of Gene Expression at Sea Level and High Altitude: A Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) Approach. [PDF]

open access: yesCureus
Alharthi SB   +9 more
europepmc   +1 more source

qRT-PCR of Microbial Biofilms

Cold Spring Harbor Protocols, 2008
INTRODUCTIONBacteria growing in biofilms often express a different subset of genes compared to the same strains growing planktonically. Quantitative reverse transcriptase real time PCR (qRT-PCR) can be used effectively to quantify the number of RNA transcripts of specific genes from bacteria growing in biofilms.
Ailyn C, Pérez-Osorio   +1 more
openaire   +2 more sources

Stem-Loop qRT-PCR–Based Quantification of miRNAs

2021
Stem-loop qRT-PCR is one of the most commonly used real-time PCR approach to quantify small non-coding RNAs such as microRNAs. The quantification method is divided in two steps. First, RNA is reverse transcribed using a specific stem-loop primer, and the resulting RT product is subsequently used as a template for quantitative real-time PCR.
Yoann, Abel, Mathieu, Rederstorff
openaire   +2 more sources

qRT-PCR of Small RNAs

2010
Plant small RNAs are a class of 19- to 25-nucleotide (nt) RNA molecules that are essential for genome stability, development and differentiation, disease, cellular communication, signaling, and adaptive responses to biotic and abiotic stress. Small RNAs comprise two major RNA classes, short interfering RNAs (siRNAs) and microRNAs (miRNAs).
Varkonyi-Gasic, Erika, Hellens, Roger
openaire   +3 more sources

Gene Amplification and qRT-PCR

2014
This chapter includes methods for the use of the polymerase chain reaction (PCR) with Pseudomonas, and several specific tips for their successful application in this organism. The first part of the chapter includes methods for purifying genomic DNA from, and amplifying genes from, Pseudomonas, in addition to methods which describe how to prepare a cell
Cerith, Jones, Alain, Filloux
openaire   +2 more sources

Continuous-flow, microfluidic, qRT-PCR system for RNA virus detection

Analytical and Bioanalytical Chemistry, 2017
One of the main challenges in the diagnosis of infectious diseases is the need for rapid and accurate detection of the causative pathogen in any setting. Rapid diagnosis is key to avoiding the spread of the disease, to allow proper clinical decisions to be made in terms of patient treatment, and to mitigate the rise of drug-resistant pathogens.
B Leticia, Fernández-Carballo   +7 more
openaire   +2 more sources

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