Description:
1. Convenient for use.2. Reilable performance.
3. Accuracy: more than 99%.
4. OEM available.
ONE STEP HBEAG SERUMTEST
| 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 |
INTENDEDUSE
One Step HBeAg Test is a rapid,one step, immunochro-matographic assay for the detection ofHepatitis B e antigen (HBeAg) in human whole blood, serum orplasma. The test provides a visual, qualitative result, and isintended for professional use.
PERFORMANCECHARATERISTICS
The One Step HBeAg Test showedequivalent detectability to EIA immunoassay for HBeAg. A resultof 99% correlation to EIA test was determined by a clinicalstudy of 1000 specimens.
SPECIMENCOLLECTION
WholeBlood:
1. Collect whole blood specimensfollowing regular clinical laboratory peocedures.
2. Heparinized capillary tubesmust be used for collecting whole blood samples. Do not usehemolyzed blood samples.
3. Whole blood specimens shouldbe used immediately after collection.
Serum orPlasma:
1. Collect serum or plasmaspecimens following regular clinical laboratoryprocedures.
2. only those specimens that areclean, clear and with good fluidity can be used for theaassay.
3. Those specimens that areapparently hemolyzed, extremely thickened or with very high fatlevel are NOT suitable for the assay.
4. Storage: A specimen should berefrigerated if not used the same day of collection. Specimensshould be frozen if not used within 3 days of collection. Avoidfrezing and thawing the specimens more than 2-3 times beforen use.0.1% of sodium azide can be added to specimen as preservativewithout affectiong the results of the assay.
TEST PROCEDURE
1. Bring all reagents andspecimens to room temperature.
2. Remove the test strip from thefoil pouch and place on a clean dry surface.
3. Identify the test strip foreach specimen or control.
4. Apply at least 80ul ofspecimen to the sample pad behind the (↓↓↓) mark at the bottom oftest strip.
5. Interpret test results at 15minutes.
Caution: Use adisposable pipette tip for each transfer to avoidcross-contamination
It is recommended to run a knownpositive control and negative control in each performance to ensurethe assay procedure.
INTERPRETATION OFRESULTS
Do not interpret theresults after 20 minutes.
POSITIVE: Inaddition to the control band, a purplish red test band also appearson the test region.
NEGATIVE: only onepurplish red test band appears on the control region.
INVALID:Neither test band nor control band appears. The specimen should betested again.
aboutUS
we have exportedour in vitro rapid diagnostic test and lab equipment to over 50countries.
OurAim:
——Letevery family benefit from our convenient and reliable diagnosticproducts and services.
——Letour lab equipment be used in every laboratory of theworld.
Our Values onQuality:
——Delivers customer value in all in allprojects, services and processes;
——Givesquality at least as much consideration as schedules and budgetswhen day-to-day choices need to be made;
——Drives QMS results to the bottom line in termsof defect reduction and financial benefits;
——Allocatesresources to achieve quality execution.
Our product have gotISO13485 & ISO9001certification
If you need highquality product at competitive price, good after-sale service, goodsupply chain —— Please contact us without hesitation or visit ourwebsite at www.accubiotech.com
