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Brand: ProteoGenix

Anti- Human IgG (anti-Monkeypox Virus M1R) ELISA Kit

629.00

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Anti- Human IgG (anti-Monkeypox Virus M1R) ELISA Kit

Anti- Human IgG (anti-Monkeypox Virus M1R) ELISA Kit

Product name Anti- Human IgG (anti-Monkeypox Virus M1R) ELISA Kit
Delivery condition Blue ice (+4°)
Storage condition The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 10% prior to the expiration date under appropriate storage condition.
Brand ProteoGenix
Size 1 kit
Reference KPTX102
Note For research use only.
Sample type Plasma, Serum
Immunogen M1R
Background information Array

Introduction

The Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit is a highly sensitive and specific diagnostic tool used for the detection of Monkeypox Virus (MPXV) infections in humans. This ELISA kit is designed to detect the presence of anti-MPXV IgG antibodies in human serum, plasma or cell culture supernatants.

Structure of the Kit

The Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit is composed of several components, including a 96-well microplate coated with recombinant MPXV M1R protein, enzyme-conjugated anti-human IgG antibody, and a substrate solution. The microplate is divided into 12 strips, each containing 8 wells, allowing for the analysis of up to 96 samples simultaneously. The kit also includes a positive and negative control, as well as a wash buffer and a stop solution.

Activity of the Kit

The Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit works on the principle of enzyme-linked immunosorbent assay (ELISA). The M1R protein, which is a highly conserved immunodominant antigen of MPXV, is immobilized on the surface of the microplate. When a sample containing anti-MPXV IgG antibodies is added to the microplate, the antibodies bind to the M1R protein. The microplate is then washed to remove any unbound components. The enzyme-conjugated anti-human IgG antibody is then added, which binds to the anti-MPXV IgG antibodies that are already attached to the M1R protein. After another wash step, the substrate solution is added, which reacts with the enzyme to produce a color change. The intensity of the color is directly proportional to the amount of anti-MPXV IgG antibodies present in the sample. The reaction is stopped by the addition of the stop solution, and the absorbance of each well is measured using a microplate reader.

Application of the Kit

The Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit has several applications in the field of infectious disease research and diagnosis. It is primarily used for the detection of MPXV infections in humans. MPXV is a zoonotic virus that can cause a severe and often fatal illness in humans. It is closely related to the more well-known smallpox virus and is classified as a potential bioterrorism agent. The Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit is a valuable tool for the early detection and monitoring of MPXV infections, as well as for epidemiological studies.

This ELISA kit can also be used for the evaluation of the immune response to MPXV vaccines. It can detect the presence of anti-MPXV IgG antibodies in vaccinated individuals, providing valuable information on the effectiveness of the vaccine.

Furthermore, the Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit can be used for the screening of blood donors, as well as for the confirmation of suspected MPXV cases in clinical settings. It is a reliable and cost-effective method for the detection of anti-MPXV IgG antibodies in human samples.

Conclusion

In summary, the Anti-Human IgG (anti-Monkeypox Virus M1R) ELISA Kit is a highly sensitive and specific diagnostic tool for the detection of MPXV infections in humans. Its simple and efficient design, along with its multiple applications, make it an essential tool for researchers and healthcare professionals working in the field of infectious diseases. With its ability to accurately detect anti-MPXV IgG antibodies in human samples, this ELISA kit is a valuable asset in the fight against MPXV and other related viruses.

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