Monkeypox Virus Antigen Rapid Test Kit
Results in 20 minutes from swab or blood sample
Product Overview
The Monkeypox Virus Antigen Rapid Test Kit is an in vitro diagnostic device based on the immunochromatographic (colloidal gold) method. It is designed for the qualitative detection of Monkeypox Virus (MPXV)-specific antigens (such as the A29L protein) in human nasopharyngeal swabs, oropharyngeal swabs, skin lesion exudate, or blood samples. This product provides a simple and rapid on-site screening solution for preliminary detection and auxiliary diagnosis of MPXV infection, suitable for various medical and public health scenarios.
Detection Principle & Target
The test employs a sandwich immunochromatographic principle. The test line (T line) and control line (C line) on the strip are pre-coated with specific monoclonal antibodies against the MPXV antigen. If the sample contains the MPXV antigen, it will bind to the gold-conjugated antibody on the conjugate pad. This complex then migrates and is captured by the antibodies on the T line, forming a visible colored line. The appearance of the C line indicates the test procedure is valid. This technology primarily targets antigens expressed early in MPXV infection, facilitating early-stage screening.
Key Features & Advantages
- Rapid & User-Friendly: Requires no complex instruments or specialized laboratory environment. Trained personnel can perform the test with minimal training. The entire process takes only 15-20 minutes to obtain visual results, significantly reducing wait times. Crucial for rapid response and triage during outbreaks or in resource-limited settings.
- High Sensitivity & Specificity: Utilizes high-affinity, highly specific paired monoclonal antibodies for excellent recognition of MPXV antigens. Laboratory data indicates detection sensitivity for the recombinant A29L protein as low as 20 pg/mL. Shows no cross-reactivity with other common pathogens like Variola virus, Vaccinia virus, Varicella-Zoster virus, or Herpes Simplex virus, ensuring accurate results.
- Multiple Sample Compatibility: Compatible with various sample types including skin lesion swabs (from vesicles, pustules, crusts), nasopharyngeal swabs, oropharyngeal swabs, whole blood, serum, and plasma, offering flexibility for different clinical situations and sampling conditions.
- Broad Application Scenarios: Suitable for healthcare facilities, disease control & public health settings, primary care & resource-limited areas, and targeted screening in potential outbreak settings.
Performance & Clinical Value
Antigen detection shows good performance when the viral load is high (typically corresponding to a low Ct value in PCR tests). As an effective screening tool, it enables timely identification of suspected cases, guides isolation measures, and prompts confirmatory testing, playing a significant role in interrupting chains of transmission.
Quality Control & Stability
The product is manufactured under a strict quality management system. The built-in control line (C line) ensures the validity of each test. The kit maintains good stability under specified storage conditions (4-30°C in a cool, dry place) with a typical shelf life of 24 months.
Customization & Support Services
We offer comprehensive OEM/ODM services and can provide in-depth customization support based on your market needs and brand strategy:
- Branding & Packaging Customization: Full customization of brand logos, exclusive designs, and multilingual text for outer boxes, foil pouches, and instruction manuals.
- Packaging Design Assistance: Our team can assist in developing packaging solutions that comply with target market regulations and aesthetic trends.
- Flexible Supply: We support orders of all scales, from small batches to large-scale procurement, with a stable supply chain guarantee.
Product Images
Important Notice
The test result is for the auxiliary diagnosis of MPXV infection. A positive result suggests a possible infection but requires comprehensive assessment by healthcare professionals based on clinical presentation and epidemiological history. Final confirmation should rely on nucleic acid test (e.g., PCR) results. A negative result does not completely rule out infection, especially in the early stages or with low viral load. Repeat testing or molecular confirmation is recommended if necessary.
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