Rapid HBeAG Test kits/strips

1. Convenient for use. 2. Reliable performance. 3. Accuracy: more than 99%. 4. OEM avaliable.

ONE STEP HBEAG SERUM TEST

Catalog No.	Product Name	Specimen	Note
ABT-IDT-A9	HBeAg Serum Strip	Serum
ABT-IDT-B9	HBeAg Serum Cassette	Serum
ABT-IDT-A81	HBeAg Whole Blood Strip	Whole Blood
ABT-IDT-B81	HBeAg Whole Blood Cassette	Whole Blood

INTENDED USE

One Step HBeAg Test is a rapid, one step,  immunochro-matographic assay for the detection of Hepatitis B e antigen (HBeAg) in  human whole blood, serum or plasma. The test provides a visual, qualitative result, and is intended for professional use.

PERFORMANCE CHARATERISTICS

The One Step HBeAg Test showed equivalent detectability to EIA immunoassay for HBeAg. A result of  99% correlation to EIA test was determined by a clinical study of 1000 specimens.

SPECIMEN COLLECTION

1. Either serum or plasma may be used in the test.

2. Anticoagulants typically used for blood collection do not interfere with this test. Remove the serum or plasma from the clot or red cells respectively. Remove the serum or plasma from the clot or red cells respectively, as soon as possible to avoid hemolysis.

3. Specimens that are apparently hemolyzed, extremely thickened or with very high fat level are NOT suitable for the assay. Specimens containing particulate matter may give inconsistent results ans should be clarified before testing.

4. If specimen are to be stored, they should be refrigeraed at 2-8°c. For long term storage(over 3 days), the specimens should be frozen.

5. If specimens are to be shipped, they should be packed in compliance with federal regulation covering the transportation of etiologic agents.

6. Avoid frequent (more than 3 times) thaw-and-freeze of specimens.

7. Up to 1% of sodium azide can be added to specimen as preservative without affecting the results of assay.

TEST PROCEDURE

1. Bring all reagents and specimens to room temperature.

2. Remove the test strip from the foil pouch and place on a clean dry surface.

3. Identify the test strip for each specimen or control.

4. Apply at least 80ul of specimen to the sample pad behind the (↓↓↓) mark at the bottom of the test strip.

5. Interpret test results at 15 minutes.

Caution: Use a disposable pipette tip for each transfer to avoid cross-contamination.

It is recommeded to run a known positive control and negative control in each performance to ensure the assay procedure.

INTERPRETATION OF RESULTS

Do not interpret the results after 20 minutes.

POSITIVE: In addition to the control band, a purplish red test band also appears on the test region.

NEGITIVE: only one purplish red test band appears on the contro; region.

INVALID: Neither test band nor control band appears. The specimen should be tested again.

ABOUT US

we have exported our in vitro rapid diagnostic test and lab equipment to over 50 countries.

Our Aim:

——Let every family benefit from our convenient and reliable diagnostic products and services.

——Let our lab equipment be used in every laboratory of the world.

Our Values on Quality:

——Delivers customer value in all in all projects, services and processes;

——Gives quality at least as much consideration as schedules and budgets when day-to-day choices need to be made;

——Drives QMS results to the bottom line in terms of defect reduction and financial benefits;

——Allocates resources to achieve quality execution.

 

Our product have got ISO13485 & ISO9001 certification

 

If you need high quality product at competitive price, good after-sale service, good supply chain —— Please contact us without hesitation or visit our website at www.accubiotech.com

Rapid HBeAG Test kits/strips