Blocking dot-ELISA, using a monoclonal antibody for detection of antibodies to bluetongue virus in bovine and ovine sera
Author:
Publisher
Elsevier BV
Subject
Virology
Reference25 articles.
1. Simple and rapid dot-enzyme immunoassay for visual detection of rinderpest antibodies in bovine and caprine sera
2. Dot-enzyme immunoassay for visual detection of antibodies to pseudorabies virus in swine serum
3. Comparison of competitive and indirect enzyme-linked immunosorbent assays for detection of bluetongue virus antibodies in serum and whole blood
4. Use of monoclonal antibody in a blocking ELISA to detect group specific antibodies to bluetongue virus
5. Nitrocellulose-enzyme-linked immunosorbent assay (NC-ELISA) — A sensitive technique for the rapid visual detection of both viral antigens and antibodies
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3. Comparative immuno-reactivity of recombinant non-structural protein 2 fragments (N- and C- terminus) to detect bluetongue viral antibodies in small ruminant serum samples;Small Ruminant Research;2019-03
4. Immuno-reactivity of recombinant non-structural protein 3 N-terminus (rNS3Nt) in indirect-ELISA for detection of bluetongue viral antibodies in serum samples;The Indian Journal of Animal Sciences;2017-11-17
5. Production of recombinant non-structural protein-3 hydrophobic domain deletion (NS3ΔHD) protein of bluetongue virus from prokaryotic expression system as an efficient diagnostic reagent;Biologicals;2016-09
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