cTnI Rapid Test
(Colloidal Gold Assay)
Intended Use
cTnI Rapid Test (Colloidal Gold Assay) is intended for in vitro qualitative and semi-quantitative determination of cardiac Troponin I (cTnI) in serum, plasma or whole blood. This test is used as an aid in the diagnosis of myocardial injury such as Acute Myocardial Infarction (AMI), Unstable Angina, Acute Myocarditis and Acute Coronary Syndrome (ACS).
Contents
A kit contains:
Package specifications: 25 tests/box, 10 tests/box
1. Getein cTnI test card in a sealed pouch with desiccant
2. Disposable pipet
3. User manual: 1 piece/box
4. Standard colorimetric card: 1 piece/box
5. Whole blood buffer: 1 bottle/box
Note: Do not mix or interchange different batches of kits.
STORAGE AND STABILITY
Store the test card at 4~30ºC with a valid period of 24 months. Use the test card within 1 hour once the foil pouch is opened.
Store the sample diluent at 0~30ºC with a valid period of 24 months.
Store the sample diluent at 2~8ºC for better results.
TEST PROCEDURE
1. Collect specimens according to user manual.
2. Test card, sample and reagent should be brought to room temperature before testing.
3. Remove the test card from the sealed pouch immediately before use. Label the test card with patient or control
identification.
4. Put the test card on a clean table, horizontally placed.
5. Using sample transfer pipette, deliver
80 μl of sample (or 3 drops of sample when using disposable pipet) into the sample port on the test card (for whole blood sample, one drop of whole blood buffer must be added after loading 80 μl sample on the test card).
6.
Read the results visually in 15 minutes. For semiquantitative interpretation of results, please refer to the
standard colorimetric card.
Test Results
Contact:
Getein Biotech, Inc.
Add.: No.9 Bofu Road, Luhe District, Nanjing (211505) China.
Web: http://getein001.en.made-in-china.com
Audited Supplier 
){kind=link}
){kind=link}