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Brand: ProteoGenix

Monkeypox Virus (MPXV) M1R Antigen ELISA Kit

Assay type:
Quantitative
Detection method:
Colorimetric
Recovery:
80-120%

$749.00

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Monkeypox Virus (MPXV) M1R Antigen ELISA Kit

Monkeypox Virus (MPXV) M1R Antigen ELISA Kit

Product name Monkeypox Virus (MPXV) M1R Antigen ELISA Kit
Delivery condition Blue ice (+4°C)
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 KPTX107
Note For research use only.
Sample type Plasma, Serum
Immunogen M1R
Assay type Quantitative
Detection method Colorimetric
Recovery 80-120%

The Structure of Monkeypox Virus (MPXV) M1R Antigen ELISA Kit

The Monkeypox Virus (MPXV) M1R Antigen ELISA Kit is a highly specialized and sensitive diagnostic tool used to detect the presence of the M1R antigen in samples from patients suspected of having monkeypox virus infection. The kit is based on the enzyme-linked immunosorbent assay (ELISA) technique, which utilizes antibodies to specifically bind and detect the M1R antigen.

The kit contains all the necessary components for the ELISA, including pre-coated microplates, wash and dilution buffers, enzyme-conjugated anti-M1R antibodies, and a chromogenic substrate for detection. The M1R antigen is immobilized on the surface of the microplate wells, allowing for efficient capture of the antigen during the assay.

The Activity of Monkeypox Virus (MPXV) M1R Antigen ELISA Kit

The Monkeypox Virus (MPXV) M1R Antigen ELISA Kit is designed to detect the presence of the M1R antigen, a protein found on the surface of the monkeypox virus. The kit works by utilizing specific antibodies that bind to the M1R antigen, allowing for its detection and quantification.

During the assay, patient samples are added to the microplate wells and incubated, allowing for any M1R antigen present in the sample to bind to the pre-coated antibodies. After washing away any unbound material, the enzyme-conjugated anti-M1R antibodies are added, which bind to the captured antigen. Finally, the chromogenic substrate is added, and the color change produced is measured and compared to a standard curve, allowing for the quantification of the M1R antigen in the sample.

The Application of Monkeypox Virus (MPXV) M1R Antigen ELISA Kit

The Monkeypox Virus (MPXV) M1R Antigen ELISA Kit has a wide range of applications in the diagnosis and monitoring of monkeypox virus infection. The kit can be used to detect the presence of the M1R antigen in various sample types, including blood, serum, and tissue samples.

The most common application of the kit is in the diagnosis of acute monkeypox virus infection. The presence of the M1R antigen in patient samples confirms the presence of the virus and aids in the early detection and treatment of the disease. The kit can also be used for the serological monitoring of patients during and after treatment, as the levels of M1R antigen can indicate the effectiveness of therapy.

In addition to its diagnostic applications, the Monkeypox Virus (MPXV) M1R Antigen ELISA Kit also has potential therapeutic applications. The M1R antigen has been identified as a potential therapeutic target, and the kit can be used to screen for potential inhibitors of the virus. This could lead to the development of new antiviral drugs to treat monkeypox virus infection.

In conclusion, the Monkeypox Virus (MPXV) M1R Antigen ELISA Kit is a highly sensitive and specific diagnostic tool for the detection of the M1R antigen in samples from patients suspected of having monkeypox virus infection. Its wide range of applications makes it a valuable tool for both diagnosis and potential therapeutic development.

  • Pandiaraj Kanagavalli, Ragi Adham Elkaffas, Shimaa Eissa, Ultrasensitive electrochemical biosensor for the simultaneous detection of the two monkeypox virus antigens M1R and A29 using reduced graphene oxide-ZIF-8 nanocomposite, Chemical Engineering Journal, Volume 516, 2025, 164015, ISSN 1385-8947, https://doi.org/10.1016/j.cej.2025.164015.

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