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Fiatest Cardiac Troponin I (cTnI) Test Use By fluorescence Immunoassay Analyzer In Human whole blood /serum /plasma
A rapid test for measuring Cardiac Troponin I (cTnI) in whole blood /serum /plasma with the use of FiatestTM fluorescence Immunoassay Analyzer. For professional in vitro diagnostic use only.
Product Name:
Fiatest Cardiac Troponin I (cTnI) Test Use By Fluorescence Immunoassay Analyzer In Human Whole Blood /serum /plasma
Format:
Cassette
Certificate:
CE
Pack:
10T/25T
Shelf Life:
2 Years
Principle:
Fluorescence Immunoassay
Specimen:
WB/S/P
Reading Time:
15 Minutes
Storage Temperature:
4-30℃
Cut-Off:
0.5 Ng/mL
Application And Description:
Cardiac Troponin I (cTnI) is a protein found in cardiac muscle with a molecular weight of 22.5 kDa[1].Troponin I is part of a three subunit complex comprising of Troponin T and Troponin C. Along with tropomyosin, this structural complex forms the main component that regulates the calcium sensitive ATPase activity of actomyosin in striated skeletal and cardiacmuscle[2].After cardiac injury occurs, Troponin I is released into the blood 4-6 hours after the onset of pain. The release pattern of cTnI is similar to CK-MB, but while CK-MB levels return to normal after 72 hours, Troponin I remains elevated for 6-10 days, thus providing for a longer window of detection for cardiac injury. The high specificity of cTnI measurements for the identification of myocardial damage has been demonstrated in conditions such as the perioperative period, after marathon runs, and blunt chest trauma[3].cTnI release has also been documented in cardiac conditions other than acute myocardial infarction (AMI) such as unstable angina, congestive heart failure, and ischemic damage due to coronary artery bypass surgery[4].Because of its high specificity and sensitivity in the myocardial tissue, Troponin I has recently become the most preferred biomarker for myocardial infarction.
How to use?
Refer to FiatestTM Fluorescence Immunoassay Analyzer Operation Manual for the complete instructions on use of the Test. The test should be conducted at room temperature.
Allow the test, specimen, buffer and/or controls to reach room temperature (15-30 °C) prior to testing.
1. Turn on the Analyzer power. Then according to the need, select “standard test”or“Quick test” mode.
2. Take out the ID card and insert it into the Analyzer port.
3. Serum/plasma: Transfer 75μL serum/plasma into the buffer tube, mix the specimen and the buffer well.Whole blood: Transfer 75μL whole blood into the buffer tube with pipette; mix the specimen and the buffer well.
4. Add diluted specimen with a Pipette: Pipette 85μL diluted specimen into the sample well. Start the timer at the same time.
5. There are two test modes for FiatestTM Fluorescence Immunoassay Analyzer, Standard Test mode and Quick Test mode. Please refer to the user manual of FiatestTM Fluorescence Immunoassay Analyzer for details.
“Quick test” mode: Insert the test cassette into the Analyzer at 15 minutes after sample application and click "New test ", the Analyzer will automatically give the test result after a few seconds.
“Standard test” mode: Insert the test cassette into the Analyzer immediately after sample application, click "New test" at the same time, the Analyzer will automatically count down 15 minutes. After the countdown, the Analyzer will give the result at once.
The Cardiac Troponin I Test Cassette (Whole Blood/Serum/Plasma) is a simple test that utilizes a combination of anti-cTnI antibody coated particles and capture reagent to detect cTnI in whole blood, serum or plasma.
INTERPRETATION OF RESULTS Results read by FiatestTM Fluorescence Immunoassay Analyzer. The result of tests for HbA1c is calculated by FiatestTM Fluorescence Immunoassay Analyzer and display the result on the screen. For additional information, please refer to the user manual of FiatestTM Fluorescence Immunoassay Analyze. Linearity range of FiatestTM HbA1c Test is 0.1-40 ng/mL.
【PERFORMANCE CHARACTERISTICS】
1. Accuracy
The test deviation is ≤±15%.
2. Sensitivity
The Cardiac Troponin I Test Cassette can detect levels of Cardiac Troponin I as low as 0.1ng/mL whole blood, serum or plasma.
3. Detection range
0.1~40 ng/mL
4. Linearity range
0.1~40 ng/mL , R≥0.990
5. Precision
C.V. ≤15%
Fast Result (15 minutes)
Simple Operation (Less Training Required)
Objective (Results Read by Analyzer)
Stringent Quality Control Insure High Accuracy
User-friendly (Simple Plug & Play Operation)
High Efficiency (Both STAT Testing and Batch Testing)
Catalogue Number
Item Name
Sample
Test Range
KIT size
FI-CTI-402
cTnI Test Cassette
WB/S/P
0.1-40 ng/mL
10T/25T
Company Details
Bronze Gleitlager
,
Bronze Sleeve Bushings
and
Graphite Plugged Bushings
from Quality China Factory
Business Type:
Manufacturer,Exporter,Trading Company
Year Established:
2009
Total Annual:
80000000-100000000
Employee Number:
1000~9999
Ecer Certification：
Verified Supplier
HANGZHOU ALLTEST BIOTECH CO.,LED has a solid foundation with top-notch industry professionals, having proven expertise in innovation management including new introductions, be it a product or be it industry transforming process developments. We have been witness to as well as been part of core teams... HANGZHOU ALLTEST BIOTECH CO.,LED has a solid foundation with top-notch industry professionals, having proven expertise in innovation management including new introductions, be it a product or be it industry transforming process developments. We have been witness to as well as been part of core teams...
