A new primer set improves the efficiency of competitive PCR–ELISA for the detection of B19 DNA
Author:
Publisher
Elsevier BV
Subject
Infectious Diseases,Virology
Reference9 articles.
1. Multiple primer pairs for polymerase chain reaction (PCR) amplification of human parvovirus B19 DNA;Durigon;J. Virol. Methods,1993
2. Analysis of B19 virus contamination in plasma pools for manufacturing by using a competitive polymerase chain reaction assay;Gallinella;Vox. Sanguis.,2002
3. Efficient parvovirus B19 DNA purification and molecular cloning;Gallinella;J. Virol. Methods,1993
4. Quantitation of parvovirus B19 DNA sequences by competitive PCR: differential hybridization of the amplicons and immunoenzymatic detection on microplate;Gallinella;Mol. Cell. Probes.,1997
5. Detection of human parvovirus B19 DNA by using the polymerase chain reaction;Koch;J. Clin. Microbiol.,1990
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1. Portable chemiluminescence multiplex biosensor for quantitative detection of three B19 DNA genotypes;Analytical and Bioanalytical Chemistry;2012-11-28
2. Colorimetric Split G-Quadruplex Probes for Nucleic Acid Sensing: Improving Reconstituted DNAzyme’s Catalytic Efficiency via Probe Remodeling;Journal of the American Chemical Society;2009-07-06
3. PCR–ELISA for High-Throughput Blood Group Genotyping;DNA and RNA Profiling in Human Blood;2009
4. Peptide Nucleic Acid–Based In Situ Hybridization Assay for Detection of Parvovirus B19 Nucleic Acids;Clinical Chemistry;2006-06-01
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