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The use of nucleic acid amplification techniques to increase the viral safety of blood.

contamination mainly due to the existence of a window period before the appearance of antibodies. Nucleic acid amplification technologies (NAT) permit a direct detection of the viral genome itself with an extreme ...

Classical swine fever virus: a second ring test to evaluate RT-PCR detection methods.

T; Hofmann, M; Thuer, B Source: Vet Microbiol, Volume 77, Issue 1-2, p.71-81 (2000) Keywords: Animals Cells, Cultured Classical Swine Fever Classical swine fever virus Diarrhea Viruses, Bovine Viral ...

Diagnosis of foot-and-mouth disease by RT-PCR: evaluation of primers for serotypic characterisation of viral RNA in clinical samples.

Aphthovirus DNA Primers Enzyme-Linked Immunosorbent Assay Evaluation Studies as Topic Foot-and-Mouth Disease Genome, Viral Reverse Transcriptase Polymerase Chain Reaction RNA, Viral Sensitivity and Specificity ...

Phylogenetic analysis of European encephalomyocarditis viruses: comparison of two genomic regions.

Sequence Belgium Capsid Cell Line Cricetinae DNA Primers Encephalomyocarditis virus Europe France Genome, Viral Greece ITALY Phylogeny Reverse Transcriptase Polymerase Chain Reaction Rodentia Swine Abstract: ...

Classical swine fever virus is genetically stable in vitro and in vivo.

Keywords: Animals Base Sequence Cell Line Classical Swine Fever Classical swine fever virus Conserved Sequence DNA, Complementary Genetic Variation Genome, Viral Phylogeny Reverse Transcriptase Polymerase ...

Differentiation of the seven serotypes of foot-and-mouth disease virus by reverse transcriptase polymerase chain reaction.

Proteins Cross Reactions DNA Primers Moloney murine leukemia virus polymerase chain reaction RNA, Viral RNA-Directed DNA Polymerase Serotyping Species Specificity Abstract: A strategy for reverse ...

Rapid diagnosis of encephalomyocarditis virus infections in pigs using a reverse transcription-polymerase chain reaction.

located in a conserved region of the 3D gene of the viral genome, was developed and tested on 114 different EMCV isolates. The identity of the respective amplicons was confirmed by sequencing. The potential ...

Polymerase chain reaction-mediated cloning and in vitro translation of the genes coding for the structural proteins of hog cholera virus.

Keywords: Base Sequence Classical swine fever virus Cloning, Molecular Molecular Sequence Data Pestivirus polymerase chain reaction Protein Biosynthesis Viral Structural Proteins Abstract: After amplification ...

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