Seneca Valley virus, SVV VP2 antibody and antigen (recombinant protein)
Diagnostic anti-Seneca Valley virus, SVV VP2 antibodies pairs and antigen for animal health (animal Swine/Porcine/Pig infectious disease idiopathic vesicular disease) 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-P095-Tg001-Ag01 | Recombinant Seneca Valley virus, SVV VP2 protein | $3090.00 |
GMP-VT-P095-Tg001-Ab01 | Anti-Seneca Valley virus, SVV VP2 mouse monoclonal antibody (mAb) | $3090.00 |
GMP-VT-P095-Tg001-Ab02 | Anti-Seneca Valley virus, SVV VP2 mouse monoclonal antibody (mAb) | $3090.00 |
GMP-VT-P095-Tg001-Ab03 | Anti-Seneca Valley virus, SVV VP2 human monoclonal antibody (mAb) | $3090.00 |
GMP-VT-P095-Tg001-Ab04 | Anti-Seneca Valley virus, SVV VP2 human monoclonal antibody (mAb) | $3090.00 |
Size: 1mg | 10mg | 100mg
Product Description
Cat No. | GMP-VT-P095-Tg001-Ag01 |
Product Name | Recombinant Seneca Valley virus, SVV VP2 protein |
Pathogen | Seneca Valley virus, SVV |
Expression platform | E.coli |
Isotypes | Recombinant Antigen |
Bioactivity validation | Anti-Seneca Valley virus, SVV VP2 antibodies binding, Immunogen in Sandwich Elisa, lateral-flow tests, and other immunoassays as control material in Seneca Valley virus, SVV level test of animal Swine/Porcine/Pig infectious disease with idiopathic vesicular disease. |
Tag | His | Product description | Recombinant Seneca Valley virus, SVV VP2 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-P095-Tg001-Ab01,GMP-VT-P095-Tg001-Ab02 |
Pathogen | Seneca Valley virus, SVV |
Product Name | Anti-Seneca Valley virus, SVV VP2 mouse monoclonal antibody (mAb) |
Expression platform | CHO |
Isotypes | Mouse IgG |
Bioactivity validation | Recombinant Seneca Valley virus, SVV VP2 antigen binding, ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Seneca Valley virus, SVV antibodies in Seneca Valley virus, SVV level test of animal Swine/Porcine/Pig infectious disease with idiopathic vesicular disease. |
Product description | Anti-Seneca Valley virus, SVV VP2 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-Seneca Valley virus, SVV 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-P095-Tg001-Ab03,GMP-VT-P095-Tg001-Ab04 |
Pathogen | Seneca Valley virus, SVV |
Product Name | Anti-Seneca Valley virus, SVV VP2 human monoclonal antibody (mAb) |
Expression platform | CHO |
Isotypes | Human lgG1 |
Bioactivity validation | Recombinant Seneca Valley virus, SVV VP2 antigen binding, ELISA validated as capture antibody and detection antibody. Pair recommendation with other anti-Seneca Valley virus, SVV antibodies in Seneca Valley virus, SVV level test of animal Swine/Porcine/Pig infectious disease with idiopathic vesicular disease. |
Product description | Anti-Seneca Valley virus, SVV VP2 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
Seneca Valley virus (SVV) is a small RNA virus that belongs to the Picornaviridae family. This family comprises numerous small, non-enveloped RNA viruses that can cause a broad range of diseases in both humans and animals. SVV was first identified in 2002 in pigs with vesicular disease and has since been detected in multiple hosts, including cattle and humans.
The genome of SVV consists of a single positive-sense RNA molecule encoding a polyprotein that is cleaved by viral proteases into individual functional proteins. The capsid protein VP1 is the major structural protein of the virus. SVV is able to infect multiple hosts and can cause vesicular disease and fever in swine, as well as aseptic meningitis in humans.
The clinical symptoms of SVV infection are variable and depend on the host species. In pigs, the disease is characterized by vesicular lesions on the skin, particularly the snout, mouth, and feet. In some cases, the disease can progress to systemic infection, which may result in death. In humans, the most common symptom of SVV infection is aseptic meningitis, which is usually self-limiting and resolves within a few days without any specific treatment.
Diagnostic methods for SVV infection include nucleic acid amplification assays, such as Reverse Transcriptase Polymerase Chain Reaction (RT-PCR), real-time RT-PCR, and serological assays such as Enzyme-Linked Immunosorbent Assay (ELISA) and Virus Neutralization Test (VNT). These methods primarily target the genes of the viral RNA genome, specifically the 5'UTR, VP1, and 3Dpol genes.
Prevention and control measures for SVV infection vary depending on the host species. In pigs, good biosecurity practices, such as quarantining new animals, maintaining proper sanitation, and controlling insect vectors, are recommended to prevent SVV transmission. In humans, the best way to prevent infection is to avoid contact with infected animals and practice good hygiene, such as washing hands frequently with soap and water.
In conclusion, Seneca Valley virus (SVV) is a small RNA virus that can cause vesicular disease and fever in swine, as well as aseptic meningitis in humans. The clinical symptoms of SVV infection are variable and depend on the host species. Diagnostic methods for SVV infection primarily target the genes of the viral RNA genome, specifically the 5'UTR, VP1, and 3Dpol genes. Prevention and control measures for SVV infection vary depending on the host species and include good biosecurity practices and practicing good hygiene.
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