Rapid Results

Cytomegalovirus (CMV) IgG/IgM Antibody Rapid Test

Rapid detection of IgG and IgM antibodies to Cytomegalovirus (CMV) in human serum or plasma.

CE Certified
ISO 13485
Main image of Cytomegalovirus (CMV) IgG/IgM Antibody Rapid Test

Why Choose reOpenTest Infectious Disease Kits?

Our tests are engineered for accuracy, reliability, and ease of use, ensuring confidence in every result.

Fast Testing

Provides results within 15-20 minutes.

Simple Procedure

Easy to use with minimal training required.

Dual Detection

Detects both IgG and IgM antibodies.

Product Overview

The Cytomegalovirus (CMV) IgG/IgM Antibody Rapid Test is a qualitative immunoassay for the simultaneous detection of IgG and IgM antibodies to CMV in human serum or plasma. This test provides results within 15-20 minutes, aiding in the diagnosis of acute or past CMV infection.

Technical Specifications

Detection Target CMV IgG/IgM Antibodies
Sample Type Serum or Plasma
Methodology Immunochromatography
Detection Range Qualitative (Positive/Negative)
Reaction Time 15-20 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect serum or plasma sample.
  2. Apply sample to the test device.
  3. Wait 15-20 minutes.
  4. Read and interpret the results.

Result Interpretation

Positive Result
Positive: Visible lines for IgM and/or IgG indicate a positive result for CMV antibodies.
Negative Result
Negative: Only the control line is visible, indicating a negative result.
Invalid Result
Invalid: If the control line is not visible, the test is invalid and should be repeated.

Frequently Asked Questions

The presence of CMV IgM antibodies generally indicates a recent or acute CMV infection. It's crucial in diagnosing primary infections, especially in pregnant women.

The detection of CMV IgG antibodies suggests past exposure to CMV. This information can be useful in assessing the risk of CMV reactivation in immunocompromised patients.

Conflicting results should be confirmed with more definitive laboratory methods such as ELISA or PCR. Clinical context is essential for correct interpretation.

Technical Documents

Download product inserts and brochures for detailed information.

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