Cargando…
PCR amplification of a triple-repeat genetic target directly from whole blood in 15 minutes as a proof-of-principle PCR study for direct sample analysis for a clinically relevant target
BACKGROUND: Most PCR-based diagnostics are still considered time- and labor-intensive due to disparate purification, amplification, and detection steps. Advancements in PCR enzymes and buffer chemistry have increased inhibitor tolerance, facilitating PCR directly from crude samples. Obviating the ne...
Autores principales: | Connelly, Christopher M, Porter, Laura R, TerMaat, Joel R |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411754/ https://www.ncbi.nlm.nih.gov/pubmed/25495904 http://dx.doi.org/10.1186/s12881-014-0130-5 |
Ejemplares similares
-
Rapid semi-automated quantitative multiplex tandem PCR (MT-PCR) assays for the differential diagnosis of influenza-like illness
por: Szewczuk, Elektra, et al.
Publicado: (2010) -
Comparison of nested PCR and real time PCR of Herpesvirus infections of central nervous system in HIV patients
por: Drago, Lorenzo, et al.
Publicado: (2004) -
Detection of group a streptococcal pharyngitis by quantitative PCR
por: Dunne, Eileen M, et al.
Publicado: (2013) -
Development and Validation of Two RT-qPCR Diagnostic Assays for Detecting Severe Acute Respiratory Syndrome Coronavirus 2 Genomic Targets across Two Specimen Types
por: Miller, Eric W., et al.
Publicado: (2022) -
Sequential multiplex PCR assay for determining capsular serotypes of colonizing S. pneumoniae
por: Jourdain, Sarah, et al.
Publicado: (2011)