Dual Antibody Detection

Chlamydia IgG/IgM Antibody Rapid Test

Simultaneously detects Chlamydia trachomatis IgG and IgM antibodies in serum or plasma.

CE Certified
ISO 13485
Main image of Chlamydia 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.

Rapid Results

Results in 15 minutes for quick diagnosis.

Serum or Plasma

Suitable for use with serum or plasma samples.

High Sensitivity

Highly sensitive and specific for Chlamydia antibodies.

Product Overview

The Chlamydia IgG/IgM Antibody Rapid Test is a qualitative immunoassay for the simultaneous detection of IgG and IgM antibodies to Chlamydia trachomatis in human serum or plasma. Providing results within 15 minutes, this rapid test aids in the early diagnosis of Chlamydia infection, facilitating point-of-care testing and improving patient management.

Technical Specifications

Detection Target Chlamydia trachomatis IgG/IgM antibodies
Sample Type Serum or Plasma
Methodology Immunochromatography
Detection Range Positive/Negative
Reaction Time 15 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 minutes.
  4. Read and interpret the results.

Result Interpretation

Positive Result
Positive: Presence of colored bands indicates Chlamydia IgG and/or IgM antibodies are detected.
Negative Result
Negative: Only the control band appears, indicating no Chlamydia antibodies are detected.
Invalid Result
Invalid: No control band appears, repeat the test with a new device.

Frequently Asked Questions

Detection of IgG and IgM antibodies helps in identifying current or past Chlamydia trachomatis infections, aiding in diagnosis and treatment decisions.

The rapid test offers a faster turnaround time compared to ELISA, making it suitable for point-of-care testing.

A positive IgM result may indicate a recent or acute Chlamydia infection. Further testing may be needed to confirm.

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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