rapid quantitative test reagents T3
GHS 1,087.19
rapid quantitative test reagents T3 for thyroid function
Description
Wondfo is a globally recognized fast growing POCT company devoted to R&D, manufacture and sales of rapid diagnostic reagents and medical devices in IVD field. Apart from the Guangzhou headquarters, Wondfo also owns one overseas lab in San Diego, one branch in Chicago and several overseas offices.“Quality is life!” is paramount in everything we do. Wondfo has won good reputation worldwide by providing premium products and professional services. We aim at serving the public, and hence people will trust Wondfo.
1. Quick and easy operation and 99% accuracy.
2. Wondfo has 27 years history, and has won good reputation around the world for good quality products and professional services..
3. Wondfo have got CE certificates, FSC certificates, ISO 9001:2008 and ISO 13485:2012 quality system certification.
4. For in vitro diagnostic use only. For self-testing use only.
PRINCIPLE
The FinecareTM T3 Rapid Quantitative Test is based on fluoresence immunoassay technology. It uses a competitive immunodetection method. When sample is added into the sample well of the Test Cartridge, the fluorescence-labeled detector T3 antibodies bind to T3 antigens in blood specimen and form immune complexes. As the complexes migrate on the nitrocellulose matrix by capillary action, it can’t be capturedby T3 antigens that have been immobilized on test strip. But the excess unbound fluorescence-labeled detector T3 antibodies are captured. Thus the more T3 in blood, the less unbound fluorescence-labeled antibodies accumulated on test strip. Signal intensity of detector T3 antibodies reflect the amount of antigens and are processed in the FinecareTM FIA System to determine the T3 concentration in blood.
TEST PROCEDURE
For complete information and operating procedures, please refer to FinecareTM FIA System Operation Manual. Test should be performed at room temperature.
Step 1: Preparation
Before testing, activate “use” in setting then save it. Ensure that the lot number of the Test Cartridge matches ID Chip as well as the Detection Buffer. Insert ID Chip into FinecareTM FIA System.
Step 2: Sampling
Draw 75 μL of whole blood or serum or plasma with a transfer pipette and add into the Detection Buffer tube.
Step 3: Mixing
Close the lid of Detection Buffer tube and mix the sample mixture thoroughly by shaking it about 10 times.
Step 4: Loading
Pipette 75 μL of sample mixture and load it into the sample well of the Test Cartridge.
Step 5: Testing
There are two test modes for FinecareTM FIA System, Standard Test mode and Quick Test mode. Please refer to the Operation Manual of FinecareTM FIA System for details.
a)For Standard Test mode: Insert the Test Cartridge onto the Test Cartridge holder of Finecare™ FIA System right after adding sample mixture to the sample well. Press “Test” to start testing. (Apply to FS-112, FS-113 and FS-205)
b) For Quick Test mode: Set the timer and count down right after adding sample mixtureinto the samplewell and leave it at room temperature for 15minutes. Then insert the Test Cartridge onto the Test Cartridge holder of Finecare™ FIA System. Press “Test” to start testing. Finecare™ FIA System will start scanning the sample-loaded Test Cartridge immediately.
(Apply to FS-112 and FS-113)
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