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Products > Infectious Disease Test > > (HBeAb)One Step Hepatitis B Envelope Antibody Test Strip HBeb-W01D
Product name : (HBeAb)One Step Hepatitis B Envelope Antibody Test Strip HBeb-W01D
Item : HBeb-W01D
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Details:

Product Name

Specimen

Format

Catalog No.

Sensitivity

Strip width

Certificate

(HBeAb)One Step Hepatitis B Envelope Antibody Test Device

Whole blood/Serum

Strip

HBeb-W01B

4NCU/ml

3.0mm

CE

HBeb-W01D

4.0mm

 

Specifications

Detection Limit:4 ncu/ml

Model No:HBeAb-W01D 

Specificity: >99% 

Specimen:Serum/Whole Blood

INTRODUCTION

Viral hepatitis is a systemic disease primarily involving the liver.Most cases of acute viral hepatitis are caused by Hepatitis A virus (HAV),Hepatitis B virus (HBV) or Hepatitis C virus (HCV).

Hepatitis B e antibody is a viral protein secreted by HBV-infected cells.The presence of antibody against hepatitis B viral e antigen is used as an indicator for early HBs antigenemia before the peak of viral replication and early convalescence when HBeAg has declined below detectable levels.It is also useful to confirm a seroconversion. The seroconversion from HBeAg positive to anti-Hbe positive indicates a reduced level of infectious virus because virus replication has decreased.

The HBeAb One Step Hepatitis B e antibody Test Device (whole blood/Serum) is a rapid test to qualitatively detect the presence of HBeAb in serum or whole blood specimen.The test utilizes a combination of monoclonal and polyclonal antibodies to selectively detect elevated levels of HBeAb in serum or whole blood.This one step test is very sensitive and only takes about 10-20 minutes.Test results are read visually without any instrument.

PRECAUTIONS
  • For professional in vitro diagnostic use only.Do not use after expiration date.
  • Do not eat,drink or smoke in the area where the specimens or kits are handled.
  • Handle all specimens as if they contain infectious agents.Observe established precautions against microbiological hazards throughout testing and follow the standard procedures for proper disposal of specimens.
  • Wear protective clothing such as laboratory coats,disposable gloves and eye protection when specimens are being tested.
  • Humidity and temperature can adversely affect results.

PROCEDURE

Allow test device,specimen,and/or controls to equilibrate to room temperature (15-30°C) prior to testing. 

  1. Bring the pouch to room temperature before opening it.Remove the test device from the sealed pouch and use it as soon as possible.Best results will be obtained if the assay is performed within one hour. 
  2. Put the test device on a clean and level surface.Hold the dropper vertically and transfer 3 full drops of serum or plasma (approx.75 mL) to specimen well (S) of the test device,and then start the timer.Avoid trapping air bubbles in the specimen well (S).See illustration below.Wait for the colored line(s) to appear. The result should be read at 15 minutes.Do not interpret the result after 20 minutes.

INTERPRETATION OF RESULTS

POSITIVE: Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).

NEGATIVE: Only one colored band appears,in the control region (C). No apparent colored band appears in the test region (T).

INVALID: Control band fails to appear.Results from any test which has not produced a control band at the specified read time must be discarded.Please review the procedure and repeat with a new test.If the problem persists,discontinue using the kit immediately and contact your local distributor.

NOTE: 

  1. The intensity of color in the test region (T) may vary depending on the concentration of analytes present in the specimen.Therefore, any shade of color in the test region should be considered positive.Note that this is a qualitative test only,and cannot determine the concentration of analytes in the specimen.
  2. Insufficient specimen volume,incorrect operating procedure or expired tests are the most likely reasons for control band failure.

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