SVANOVIR BLV gp51-Ab (2 ELISA plates)

Cat. No.: SV-104884

SVANOVIR BLV gp51-Ab
(2 ELISA plates)

For detection of specific antibodies to Bovine Leukemia Virus gp51 (Availability/distribution: Outside the U.S. and Canada) [Read more]

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The SVANOVIR BLV gp51-AB is an indirect ELISA for the detection of specific antibodies to Bovine Leukemia Virus gp51 in bovine serum, plasma and milk samples (individual and bulk tank milk). The assay is based on the gp51 envelope protein, enabling the detection of antibodies to BLV during early phase of infection.

Features and benefits:

  • Field-proven assay – used for the control of BLV in Scandinavia, Netherlands, Croatia, Canada and Australia
  • High analytical sensitivity, repeatedly proven in bulk tank milk and dilution studies
  • Standardized against the reference serum E05 (according to Directive 64/432/EEC) 
  • Semi quantitative test – paired samples used to detect cows pregnant with PI-calves
  • Accurate results in proficiency tests organized by the OIE Reference Laboratory for Enzootic Bovine Leukosis in Poland, in 2011 and 2014
  • Prescribed test method for international trade by the OIE
For up-to-date licensing information and product-specific disclaimers, see the respective handbook or user manual. Assays for veterinary use only. Regulatory requirements vary by country, product may not be available in your geographic area. PCR and ELISA kits availability/distribution: Outside the U.S. and Canada.
Pathogen type Virus
Product type Ready-to-use assay
Species Ruminants
Pathogen investigated Bovine Leukemia Virus (BLV)
Technology ELISA
Handbooks
Handbook SVANOVIR BLV gp51-Ab Confirmation (April 2021, EN)
Handbooks
Handbook SVANOVIR BLV gp51-Ab Screening (April 2021, EN)
Certificates of Analysis (CoA)

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Safety Data Sheets

Safety Data Sheets (SDS) for product components are available on request.

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1. Klintevall, K., Näslund, K., Svedlund, G., Hajdu, L., Linde, N., Klingeborn, B.(1991): Evaluation of an indirect ELISA for the detection of antibodies to bovine leukaemia virus in milk and serum. Journal of Virological Methods, Volume 33, Issue 3, August 1991, Pages 319-333.

2. Kuzmak, (2014; 2011): Bovine Enzootic Leucosis Quality Assessment Results. Reports.

3. Kramps J.A. (1994): BLV-specific antibody bovine reference serum samples. CDI-DLO, Lelystad, Netherlands, Report.

4. Jalali, A (2010): Titration of the New Standard Serum E05 for the EBL diagnostics in serum and tank milk in order to establish the size of milk pools for the SVANOVIR® BLV gp-51-Ab–ELISA. Internal Report.

5. Simard,C., Richardson,S., Dixon,P., Belanger,C., Maxwell, P. (2000): Enzyme-linked immunosorbent assay for the diagnosis of bovine leukosis: comparison with the agar gel immunodiffusion test approved by the Canadian Food Inspection Agency. The Canadian Journal of Veterinary Research; 64;pp 101-106

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For up-to-date licensing information and product-specific disclaimers, see the respective handbook or user manual. Assays for veterinary use only. Reagents for research use only, not for use in diagnostic procedures. Regulatory requirements vary by country, products may not be available in your geographic area. Trademarks: bactotype®, cador®, cattletype®, flocktype®, intype®, pigtype®, virotype® (INDICAL BIOSCIENCE GmbH) QIAGEN®, QIAamp®, QIAcube®, BioSprint®, DNeasy®, MagAttract® (QIAGEN Group). Registered names, trademarks, etc., used here, even when not specifically marked as such, are not to be considered unprotected by law. Product images may differ from the actual product. INDICAL BIOSCIENCE reserves all rights to correct any errors in the online system prior to shipping and billing. If you suspect an error in pricing, please contact us.