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| Size | 96T |
|---|---|
| Brand | ProteoGenix |
| Product type | Elisa assay kits |
| Product name | PEDV NP/Nucleoprotein ELISA Kit |
|---|---|
| Delivery condition | Blue ice (+4°C) |
| Delivery lead time in business days | 3-5 days if in stocks, 3-5 weeks if production is needed |
| Storage condition | 4°C for short term (1 week), store at -20°C to -80°C for long term(1 year); Avoid repeated freeze-thaw cycles |
| Brand | ProteoGenix |
| Note | For research use only. |
| Immunogen | NP |
| Assay type | Quantitative |
| Detection method | Colorimetric |
| Recovery | 80-120% |
The Porcine Epidemic Diarrhea Virus (PEDV) is a highly contagious and deadly virus that affects pigs, causing severe diarrhea and dehydration. The virus has caused significant economic losses in the swine industry, making it a major concern for pig farmers worldwide. In order to control and prevent the spread of PEDV, accurate and efficient diagnostic tools are crucial. The PEDV NP/Nucleoprotein ELISA Kit is a cutting-edge diagnostic tool that has been specifically designed for the detection of PEDV nucleoprotein in pig samples. In this article, we will delve into the structure, activity, and application of this advanced ELISA kit.
The PEDV NP/Nucleoprotein ELISA Kit is a sandwich enzyme-linked immunosorbent assay (ELISA) that utilizes monoclonal antibodies to specifically detect the nucleoprotein of PEDV in pig samples. The kit consists of pre-coated microplates, wash buffer, enzyme conjugate, substrate solution, and stop solution. The pre-coated microplates are coated with monoclonal antibodies that specifically bind to the nucleoprotein of PEDV. The enzyme conjugate is a horseradish peroxidase (HRP) labeled secondary antibody that binds to the captured nucleoprotein. The substrate solution contains a chromogenic substrate that produces a color change in the presence of HRP, which can be measured using a spectrophotometer. The stop solution halts the enzyme reaction and stabilizes the color development.
The PEDV NP/Nucleoprotein ELISA Kit works by utilizing the principle of sandwich ELISA. In this assay, the pre-coated microplates are first incubated with pig samples, allowing any PEDV nucleoprotein present in the sample to bind to the monoclonal antibodies. After washing away any unbound material, the enzyme conjugate is added, which binds to the captured nucleoprotein. The addition of the substrate solution leads to the development of a color change, which is directly proportional to the amount of PEDV nucleoprotein present in the sample. The intensity of the color can be measured using a spectrophotometer, and the results can be compared to a standard curve to determine the concentration of PEDV nucleoprotein in the sample.
The PEDV NP/Nucleoprotein ELISA Kit has multiple applications in both research and clinical settings. In research, the kit can be used to study the prevalence and transmission of PEDV in pig populations. It can also be used to evaluate the efficacy of vaccines and treatments against PEDV. In clinical settings, the kit can aid in the early and accurate diagnosis of PEDV infection, allowing for prompt treatment and control measures. The kit can also be used for screening and surveillance of PEDV in pig herds, helping to prevent the spread of the virus.
The nucleoprotein of PEDV is an important therapeutic target for the development of antiviral drugs and vaccines. The nucleoprotein plays a crucial role in the replication and assembly of the virus, making it an attractive target for intervention. The PEDV NP/Nucleoprotein ELISA Kit can aid in the identification and characterization of potential antiviral compounds that target the nucleoprotein, leading to the development of effective treatments for PEDV.
The PEDV NP/Nucleoprotein ELISA Kit has been extensively used in various research studies to understand the biology and pathogenesis of PEDV. It has been used to study the interaction between PEDV and host cells, as well as to investigate the immune response to the virus. The kit has also been used to evaluate the effectiveness of different disinfectants in inactivating PEDV. The high
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