Antibody Detection

Influenza A (H5N) IgG/IgM Antibody Rapid Test

Rapid detection of Influenza A (H5N) IgG/IgM antibodies in serum or plasma for infection assessment.

CE Certified
ISO 13485
Main image of Influenza A (H5N) 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.

Specific H5N Detection

Detects IgG and IgM antibodies specific to Influenza A (H5N) subtype.

Quick Turnaround Time

Provides results in 10-15 minutes for timely clinical evaluation.

Aids Treatment Decisions

Assists healthcare professionals in assessing patient exposure to H5N influenza.

Product Overview

The Influenza A (H5N) IgG/IgM Antibody Rapid Test is a qualitative immunoassay for the detection of IgG and IgM antibodies against Influenza A (H5N) subtype in human serum or plasma. This test is designed for professional use to aid in the assessment of patient exposure to H5N influenza.

Technical Specifications

Detection Target Influenza A (H5N) IgG/IgM antibodies
Sample Type Serum or Plasma
Methodology Immunochromatography
Detection Range Qualitative (Positive/Negative)
Reaction Time 10-15 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect a serum or plasma sample.
  2. Apply the sample to the test device.
  3. Add the provided buffer solution.
  4. Read the results after 10-15 minutes.
  5. Interpret the results based on the appearance of control and test lines.

Result Interpretation

Positive Result
Positive: The presence of control and one or more test lines indicates a positive result for Influenza A (H5N) IgG/IgM antibodies.
Negative Result
Negative: The presence of only the control line indicates a negative result.
Invalid Result
Invalid: If the control line does not appear, the test is invalid and should be repeated.

Frequently Asked Questions

A positive result suggests past or current exposure to the Influenza A (H5N) virus. Further confirmatory testing may be required.

This test detects antibodies, which may take time to develop after infection. Therefore, it is more suitable for assessing past exposure or immune response rather than acute diagnosis. Use a direct antigen test for acute diagnosis.

Store the test kit at 2-30u00b0C (36-86u00b0F) and protect it from freezing. Do not use the test after the expiration date.

Technical Documents

Download product inserts and brochures for detailed information.

No technical documents are available at this time. Please check back soon.

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