Zobrazeno 1 - 10
of 28
pro vyhledávání: '"G. C. Dulac"'
Publikováno v:
Journal of Veterinary Diagnostic Investigation. 5:336-340
The performance of a competitive (c) enzyme-linked immunosorbent assay (ELISA) test kit, Blueplate Special@ (BPS), commercially produced by DiagXotics (Wilton, CT) for detection of group-specific antibodies to bluetongue virus (BTV) was compared with
Publikováno v:
Journal of Virological Methods. 31:105-112
A rapid, simple dot immunoperoxidase assay (DIPA) is described for visual detection and identification of bluetongue virus (BTV) antigens in samples of infected cell culture fluid. The assay was performed using nitrocellulose (NC) paper and 'dipstick
Publikováno v:
Applied and Environmental Microbiology. 63:3916-3918
The efficacy of vapor-phase hydrogen peroxide in a pass-through box for the decontamination of equipment and inanimate materials potentially contaminated with exotic animal viruses was evaluated. Tests were conducted with a variety of viral agents, w
Publikováno v:
Journal of Veterinary Diagnostic Investigation. 5:614-616
Autor:
Richard McLaurin, R A Heckert, Soopayah Vydelingum, Isabelle Prud'homme, José Riva, G. C. Dulac, Martha J. Harding, C. Gradil
Publikováno v:
Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 8(4)
A blind panel was tested in a diagnostic evaluation of a reverse transcription (RT) polymerase chain reaction (PCR) method for detecting hog cholera virus (HCV) from pig tissues. The capability of the RT-PCR test to discriminate between HCV and relat
Publikováno v:
Journal of wildlife diseases. 31(3)
A competitive enzyme-linked immunosorbent assay (C-ELISA), using a group-specific monoclonal antibody against bluetongue virus (BTV), was applied to detect anti-BTV antibodies in serum samples from two llamas (Llama glama) experimentally infected wit
Two competitive (C) enzyme-linked immunosorbent assays (ELISAs) were developed for the detection of antibodies to vesicular stomatitis virus (VSV) in animal sera. The assays are based upon the availability of polyclonal antibodies (PAbs) from mouse a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee28e5d4019e347178bb008492ce23ab
https://europepmc.org/articles/PMC265646/
https://europepmc.org/articles/PMC265646/
Publikováno v:
Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 5(1)
Two indirect enzyme-linked immunosorbent assays (I-ELISAs) are described for the detection of bovine serum antibody to the New Jersey (NJ) and Indiana (IN) vesicular stomatitis viruses (VSV). Serum samples at a dilution of 1:200 were incubated with b
Publikováno v:
Veterinary microbiology. 31(1)
A blocking (B) dot enzyme-linked immunosorbent assay (ELISA), using a monoclonal antibody (mAb) against a group specific antigen of bluetongue virus (BTV) is described for the detection of BTV antibodies to BTV in cattle sera. Dots of BTV antigens we
Publikováno v:
Avian diseases. 35(3)
Vaccination of chickens with an oil-emulsion vaccine containing a recombinant baculovirus that expressed the hemagglutinin-neuraminidase (HN) of Newcastle disease virus (NDV)-induced hemagglutination-inhibition (HI) and virus-neutralizing antibodies