Whole Blood/Serum/Plasma Test

Hepatitis C Virus (HCV) Antibody Rapid Test Device (Whole Blood/Serum/Plasma)

Rapid HCV antibody detection in whole blood, serum, or plasma.

CE Certified
ISO 13485
Main image of Hepatitis C Virus (HCV) Antibody Rapid Test Device (Whole Blood/Serum/Plasma)

Why Choose reOpenTest Infectious Disease Kits?

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

Flexible Sample Types

Compatible with whole blood, serum, and plasma.

Quick Turnaround

Results available in 10-15 minutes.

Easy to Use

Simple lateral flow assay.

Product Overview

The Hepatitis C Virus (HCV) Antibody Rapid Test Device is a qualitative immunoassay for the detection of antibodies to HCV in human whole blood, serum, or plasma samples. This point-of-care test provides a rapid and convenient method for screening individuals for the presence of HCV antibodies, indicating past or current infection.

Technical Specifications

Detection Target HCV Antibodies
Sample Type Whole Blood, Serum, Plasma
Methodology Immunochromatography (Lateral Flow Assay)
Detection Range Positive/Negative
Reaction Time 10-15 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect a whole blood, 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.

Result Interpretation

Positive Result
Positive: The presence of a colored line indicates a positive result for HCV antibodies.
Negative Result
Negative: The absence of a colored line indicates a negative result.
Invalid Result
Invalid: If no control line appears, the test is invalid and should be repeated.

Frequently Asked Questions

Using whole blood eliminates the need for centrifugation, making it ideal for point-of-care testing in resource-limited settings.

The lateral flow assay uses specific antibodies to capture HCV antibodies in the sample, generating a visible colored line if present.

The minimum detection limit is determined by the test's sensitivity. Please refer to the product insert.

Technical Documents

Download product inserts and brochures for detailed information.

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

Partner with reOpenTest

Provide your clients and patients with reliable diagnostic solutions.
Contact us today for bulk pricing and distribution opportunities.

Become a Distributor