Basic Info.
Product Description
Product Information
One step rapid medical troponin I rapid test equipment
The Troponin I Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Tropnin I (cTnI) and its complex in human serum or plasma at the level equal or higher than 1 ng/mL. It is intended to be used as a screening test and as an aid in the diagnosis of acute myocardial infarction (AMI). Any reactive specimen with the Troponin I Rapid Test must be confirmed with alternative testing method(s) and clinical findings
1 Allow the Troponin I (cTnl) Test device, specimen, buffer, and/or controls to equilibrate to room temperature (15-30°C) prior to testing.
2 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. Place the Troponin I (cTnl) Test device on a clean and level surface.
3.
Serum/plasma | Venipuncture Whole Blood | Fingerstick Whole Blood |
Transfer 2 drops of serum or plasma (approximately 50 µL) to the specimen well (S) of the Troponin I (cTnl) Test device. | Transfer 4 drops of whole blood (approximately 100 µL) to the specimen well (S) of the test Troponin I (cTnl) Test. | Transfer 4 hanging drops of fingerstick blood/or approximately 100 µL from the capillary tube to the specimen well (S) of the Troponin I (cTnl) Test. |
4 Start the timer. Wait for the red line(s) to appear. The result should be read at 15 minutes. Do not read results after more than 20 minutes.
TEST RESULTS
Negative:One red line appears in the control line region (C). No apparent red line appears in the test line region (T).
Positive:Two distinct red lines appear. One line should be in the control line region (C) and another line should be in the test line region (T).
Invalid:Lines or control lin e fail to appear. Insufficient specimen volume or incorrect procedural techniques are t he most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact you local distributor.
Production ProcessQ1.What's the method you use to do the test?
A: Colloidal Gold Method.
Q2: What's ur MOQ ?
A: Always, for strip format, the MOQ is 5000pcs. While for cassette format, MOQ is 2000pcs, same as midstream.
Q3: What's ur packing of the tests?
A: If u choose the low cost, we will suggest u the bulk packing to go. Which means 1 test in a single pouch, then 100/40 pouches in a plastic bag, 50 bags in a carton. If u need to sell in pharmacy/chain shop or some countries which have strict requirements about the packing, u can choose to pack in a box, like 100pcs in a box, or even 1 test in a single box.
Q4: What's the main differences when comparing products from different suppliers?
A: U can compare the mainly features of the test: Accuracy, Sensitivity, Specificity, and then the Price.
Q5: Some tests can be tested with serum/plasma or with whole blood, so what's the difference?
A: Well, if the specimen is whole blood, people will need buffer, lancet and alcohol swab to help the test. If they buy all the accessories, they can test very easily at home. But if the specimen is serum/plasma, it will need centrifuge to separate serum from whole blood first. This way, it's better to use at lab or hospital. And in some words, serum/plasma test will always give a more accurate results.
Q6: How can i distinguish a good test kit?
A: U can judge from the 4facts:
1. Technical data: Such as the accuracy, specificity and sensitivity.
2. Pouch sealing: Tight enough. If the foil pouch is not sealed well, the humidity in circustance will destroy the reactivity of antibodies labeled on NC membrane. Shelf life will be shorten down.
3. Flow speed: The shorter the better?? NO!! The reaction of antibodies on NC membrane and antigens in specimen usually requires quite a while to work sufficiently. U can refer to the instruction for more accurate time.
4. Background: Good test usually gives clean background after running. If there are red smears in the reading window, it usually caused by bad colloidal gold technology or bad NC membrane. Sometimes, the defect caused false positive result in practice.
Contact Us
Promise:We will offer our good after sale service always!as we strongly believe,QUALITY and SINCERE is very important among countries cooperations!
Welcome to enquiry .Pls feel free to contact us
Contact Name:Genos Dai
E-mail:sales@diagnosbio. com