Maedi Visna Virus/ Visna virus p25 antibody and antigen (recombinant protein)

Diagnostic anti-Maedi Visna Virus/ Visna virus p25 antibodies pairs and antigen for animal health (animal Ovines/Sheep, Caprine/Goat infectious disease Maedi Visna Virus infection) testing in ELISA, colloidal gold-based Lateral flow immunoassay (LFIA), CLIA, TINIA and POCT

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Product information

Catalog No. Description US $ Price (per mg)
GMP-VT-P082-Tg001-Ag01 Recombinant Maedi Visna Virus/ Visna virus p25 protein $3090.00
GMP-VT-P082-Tg001-Ab01 Anti-Maedi Visna Virus/ Visna virus p25 mouse monoclonal antibody (mAb) $3090.00
GMP-VT-P082-Tg001-Ab02 Anti-Maedi Visna Virus/ Visna virus p25 mouse monoclonal antibody (mAb) $3090.00
GMP-VT-P082-Tg001-Ab03 Anti-Maedi Visna Virus/ Visna virus p25 human monoclonal antibody (mAb) $3090.00
GMP-VT-P082-Tg001-Ab04 Anti-Maedi Visna Virus/ Visna virus p25 human monoclonal antibody (mAb) $3090.00

Size: 1mg | 10mg | 100mg



Product Description

Cat No. GMP-VT-P082-Tg001-Ag01
Product Name Recombinant Maedi Visna Virus/ Visna virus p25 protein
Pathogen Maedi Visna Virus/ Visna virus
Expression platform E.coli
Isotypes Recombinant Antigen
Bioactivity validation Anti-Maedi Visna Virus/ Visna virus p25 antibodies binding, Immunogen in Sandwich Elisa, lateral-flow tests, and other immunoassays as control material in Maedi Visna Virus/ Visna virus level test of animal Ovines/Sheep, Caprine/Goat infectious disease with Maedi Visna Virus infection.
Tag His
Product description Recombinant Maedi Visna Virus/ Visna virus p25 proteinwas expressed in E.coli - based prokaryotic cell expression system and is expressed with 6 HIS tag at the C-terminus.
Purity Purity: ≥95% (SDS-PAGE)
Application Paired antibody immunoassay validation in sandwich Elisa, ELISA, colloidal gold-based Lateral flow immunoassay (LFIA), CLIA, TINIA, POCT and other immunoassays.
Formulation Lyophilized from sterile PBS, PH 7.4
Storage Store at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


Cat No. GMP-VT-P082-Tg001-Ab01,GMP-VT-P082-Tg001-Ab02
Pathogen Maedi Visna Virus/ Visna virus
Product Name Anti-Maedi Visna Virus/ Visna virus p25 mouse monoclonal antibody (mAb)
Expression platform CHO
Isotypes Mouse IgG
Bioactivity validation Recombinant Maedi Visna Virus/ Visna virus p25 antigen binding, ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Maedi Visna Virus/ Visna virus antibodies in Maedi Visna Virus/ Visna virus level test of animal Ovines/Sheep, Caprine/Goat infectious disease with Maedi Visna Virus infection.
Product description Anti-Maedi Visna Virus/ Visna virus p25 mouse monoclonal antibody (mAb) is a mouse monoclonal antibody produced by CHO technology. The antibody is ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Maedi Visna Virus/ Visna virus antibodies.
Purity Purity: ≥95% (SDS-PAGE)
Application Paired antibody immunoassay validation in sandwich Elisa, ELISA, colloidal gold-based Lateral flow immunoassay (LFIA), CLIA, TINIA, POCT and other immunoassays.
Formulation Lyophilized from sterile PBS, PH 7.4
Storage Store at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


Cat No. GMP-VT-P082-Tg001-Ab03,GMP-VT-P082-Tg001-Ab04
Pathogen Maedi Visna Virus/ Visna virus
Product Name Anti-Maedi Visna Virus/ Visna virus p25 human monoclonal antibody (mAb)
Expression platform CHO
Isotypes Human lgG1
Bioactivity validation Recombinant Maedi Visna Virus/ Visna virus p25 antigen binding, ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Maedi Visna Virus/ Visna virus antibodies in Maedi Visna Virus/ Visna virus level test of animal Ovines/Sheep, Caprine/Goat infectious disease with Maedi Visna Virus infection.
Product description Anti-Maedi Visna Virus/ Visna virus p25 mouse monoclonal antibody (mAb) is a human monoclonal antibody produced by CHO. The antibody is ELISA validated as capture antibody and detection antibody pair.
Purity Purity: ≥95% (SDS-PAGE)
Application Paired antibody immunoassay validation in sandwich Elisa, ELISA, colloidal gold-based Lateral flow immunoassay (LFIA), CLIA, TINIA, POCT and other immunoassays.
Formulation Lyophilized from sterile PBS, PH 7.4
Storage Store at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles.


Reference




    Validation Data


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    Pathogen Information


    Names of the Pathogen:

    The pathogen responsible for Rinderpest is known as the Rinderpest virus, with "Rinderpest" being derived from the German term for "cattle plague."

    Pathogen Classification:

    Rinderpest virus falls within the classification of viral pathogens. It is categorized in the Paramyxoviridae family, which comprises several other significant animal viruses.

    Pathogen Structure:

    The Rinderpest virus features a non-segmented, single-stranded, negative-sense RNA genome. Within its genetic makeup, various structural and non-structural proteins are encoded. The fusion (F) and hemagglutinin-neuraminidase (HN) proteins play pivotal roles in viral entry and dissemination.

    Hosts and Diseases:

    Rinderpest virus predominantly targets domestic and wild cloven-hoofed animals. It is renowned for causing Rinderpest, a highly contagious and frequently lethal disease affecting cattle, buffalo, and certain other cloven-hoofed animals.

    Diagnostic Methods:

    Several diagnostic methods are employed to detect the presence of the Rinderpest virus, including:

    1.Nucleic Acid Detection: Polymerase Chain Reaction (PCR) is a widely employed technique for detecting the virus. Specific genes, such as the nucleocapsid (N) gene, fusion (F) gene, and hemagglutinin-neuraminidase (HN) gene, are targeted for amplification and identification.

    2.Serological Tests: Enzyme-Linked Immunosorbent Assay (ELISA) is employed to detect antibodies produced in response to the virus, aiding in the diagnosis of infections.

    3.Virus Isolation: The virus can be isolated from infected tissues and subsequently cultured within a laboratory environment, facilitating further study and diagnostic purposes.

    When promoting products or solutions related to the Rinderpest virus, it is crucial to emphasize the importance of accurate and rapid diagnostic methods. These methods play a pivotal role in controlling the disease in livestock, ensuring the health and well-being of these animals. Additionally, highlighting the successful history of Rinderpest eradication through vaccination and stringent monitoring can serve as a compelling message in advocating for biopharmaceutical solutions.



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