Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein antibody and antigen (recombinant protein)

Diagnostic anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein antibodies pairs and antigen for animal health (animal Fish infectious disease Viral hemorrhagic septicemia) 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-P231-Tg001-Ag01 Recombinant Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein protein $3090.00
GMP-VT-P231-Tg001-Ab01 Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein mouse monoclonal antibody (mAb) $3090.00
GMP-VT-P231-Tg001-Ab02 Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein mouse monoclonal antibody (mAb) $3090.00
GMP-VT-P231-Tg001-Ab03 Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein human monoclonal antibody (mAb) $3090.00
GMP-VT-P231-Tg001-Ab04 Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein human monoclonal antibody (mAb) $3090.00

Size: 1mg | 10mg | 100mg



Product Description

Cat No. GMP-VT-P231-Tg001-Ag01
Product Name Recombinant Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein protein
Pathogen Viral Haemorrhagic Septicaemia Virus
Expression platform E.coli
Isotypes Recombinant Antigen
Bioactivity validation Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein antibodies binding, Immunogen in Sandwich Elisa, lateral-flow tests, and other immunoassays as control material in Viral Haemorrhagic Septicaemia Virus level test of animal Fish infectious disease with Viral hemorrhagic septicemia.
Tag His
Product description Recombinant Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein 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-P231-Tg001-Ab01,GMP-VT-P231-Tg001-Ab02
Pathogen Viral Haemorrhagic Septicaemia Virus
Product Name Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein mouse monoclonal antibody (mAb)
Expression platform CHO
Isotypes Mouse IgG
Bioactivity validation Recombinant Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein antigen binding, ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Viral Haemorrhagic Septicaemia Virus antibodies in Viral Haemorrhagic Septicaemia Virus level test of animal Fish infectious disease with Viral hemorrhagic septicemia.
Product description Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein 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-Viral Haemorrhagic Septicaemia 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-P231-Tg001-Ab03,GMP-VT-P231-Tg001-Ab04
Pathogen Viral Haemorrhagic Septicaemia Virus
Product Name Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein human monoclonal antibody (mAb)
Expression platform CHO
Isotypes Human lgG1
Bioactivity validation Recombinant Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein antigen binding, ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Viral Haemorrhagic Septicaemia Virus antibodies in Viral Haemorrhagic Septicaemia Virus level test of animal Fish infectious disease with Viral hemorrhagic septicemia.
Product description Anti-Viral Haemorrhagic Septicaemia Virus nucleocapsid (N) protein 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


    SDS-PAGE and HPLC results of GMP-VT-P231-Tg001-Ab02

    Figure 2. SDS-PAGE under reduced conditions and SEC-HPLC test result of GMP-VT-P231-Tg001-Ab02

    SDS-PAGE and HPLC results of GMP-VT-P231-Tg001-Ab03

    Figure 2. SDS-PAGE under reduced conditions and SEC-HPLC test result of GMP-VT-P231-Tg001-Ab03


    Click to get more Data / Case study about the product.



    Pathogen Information


    Aujeszky's Disease Virus (ADV), also known as Pseudorabies Virus (PRV), is a highly contagious and economically significant pathogen that primarily infects pigs. It belongs to the Herpesviridae family, which is a diverse group of enveloped, double-stranded DNA viruses that are capable of infecting a broad range of hosts, including humans.

    ADV has a complex structure that comprises multiple components, including glycoprotein B (gB), glycoprotein C (gC), glycoprotein D (gD), and glycoprotein E (gE). These proteins are encoded by the viral genome and play key roles in viral entry, replication, and immune evasion.

    The gB protein is essential for viral fusion with cell membranes, while the gC protein promotes viral attachment to host cells. The gD protein mediates virus entry into host cells by binding to specific cellular receptors, while the gE protein is important for virus assembly and release from infected cells. ADV also produces several non-structural proteins that interact with host factors, leading to viral replication and pathogenesis.

    In pigs, ADV infection causes Aujeszky's disease, which is characterized by a range of clinical signs such as anorexia, fever, respiratory distress, and nervous system disorders. The virus can establish lifelong persistence and shedding in the tonsils and nasal cavities of infected animals, leading to prolonged transmission and enhanced disease spread.

    ADV is a zoonotic pathogen, meaning it can infect humans who come into contact with infected animals or contaminated materials. Although human infections are rare, they can occur through direct or indirect contact with infected pigs or their secretions.

    To prevent and control ADV infections, various methods have been developed for its detection and diagnosis. These methods include nucleic acid-based techniques such as polymerase chain reaction (PCR) and real-time PCR, which target genes such as gB or gD and can detect viral DNA in clinical samples with high sensitivity and specificity. Additionally, virus isolation in cell culture and serological assays like enzyme-linked immunosorbent assay (ELISA) detecting anti-ADV antibodies in the blood can be used for diagnosis.

    Control measures for ADV include vaccination and biosecurity measures to prevent or limit disease transmission. Several ADV vaccines are currently available, including live attenuated and killed virus vaccines, which provide effective protection against the disease. In addition, strict biosecurity practices such as quarantine, disinfection, and limiting animal movements can help prevent or reduce the spread of the virus.

    In conclusion, Aujeszky's Disease Virus is a highly infectious and economically significant pathogen that primarily infects pigs but also has zoonotic potential. Its complex structure and interaction with the host immune system contribute to its virulence and persistence. Detection and control measures such as nucleic acid-based techniques and vaccination can help mitigate the impact of this pathogen.



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