Qualitative/Quantitative detection of cardiac Troponin I (cTnI)
Real-Time Operation
Yes
Operating Type
Manual
Size
Standard test strip size
Weight
Lightweight (single use device)
Color
White
Usage
Diagnostic use for detection of cTnI
Attributes
Single-use, fast result, easy to use, point-of-care test
Intended Use
Detection of cardiac Troponin I in whole blood, serum or plasma
Kit Contents
25 test cassettes, buffer, instructions for use
Shelf Life
12-24 months (refer to pack)
Sensitivity
High clinical sensitivity for cTnI
Storage Condition
2-30C (36-86F)
Test Time
10-15 minutes
Sample Type
Whole blood/Serum/Plasma
Test Principle
Fluorescent immunoassay, lateral flow
FIAflex cTnI FIA Test 25T About
The FIAflex cTnI FIA Test is a fluorescence immunoassay (FIA) used with an analyzer for the quantitative detection of cardiac Troponin I (cTnI) in blood samples. It is designed as an aid in diagnosing and monitoring acute myocardial infarction (AMI), also known as a heart attack.
The "25T" indicates that the kit contains 25 tests.
Key features
Quantitative results: The test provides a specific numerical value for the cTnI concentration in the sample, which is a significant clinical marker for cardiac injury.
Sample types: It can be used with human serum, plasma, or whole blood specimens.
Rapid testing: The test is designed to be completed quickly, often within 15 minutes, making it suitable for point-of-care settings and emergency departments.
High specificity: The test employs monoclonal antibodies that specifically target the cardiac troponin I antigen, leading to higher specificity compared to other cardiac markers.
Rapid and Accurate Cardiac Marker Detection
The FIAflex cTnI FIA Test leverages fluorescence immunoassay technology to deliver highly sensitive detection of cardiac Troponin I, a critical marker for cardiac events. Its quick turnaround time ensures prompt diagnostic decisions, enhancing patient care and clinical workflow efficiency in both hospital and point-of-care environments.
User-Friendly Design and Application
This portable, manual test kit contains 25 disposable cassettes and all necessary materials for immediate use. Its intuitive procedure is suitable for healthcare professionals and enables testing directly from whole blood, serum, or plasma. Clear instructions and minimal handling requirements streamline the testing process.
FAQ's of FIAflex cTnI FIA Test 25T:
Q: How does the FIAflex cTnI FIA Test detect cardiac Troponin I in blood samples?
A: The test uses a fluorescence immunoassay principle combined with lateral flow technology to accurately measure cTnI levels in whole blood, serum, or plasma. This allows rapid, sensitive, and specific detection crucial for diagnosing cardiac events.
Q: What is the recommended process for using the FIAflex cTnI FIA Test?
A: To use the test, add the specified amount of whole blood, serum, or plasma sample to the cassette, followed by the buffer. After a 10-15 minute development time, results are read using the supplied instructions, yielding either qualitative or quantitative information about cTnI levels.
Q: When should the FIAflex cTnI FIA Test be used?
A: This test should be utilized when acute myocardial infarction or cardiac injury is suspected, as rapid detection of cardiac Troponin I enables timely clinical intervention and patient management.
Q: Where can the FIAflex cTnI FIA Test be performed?
A: Due to its portability and ease of use, the test can be performed at the point of care, in clinics, emergency departments, or laboratory settings, providing flexibility for diverse clinical needs.
Q: What are the storage conditions and shelf life for this test kit?
A: The test should be stored at 2-30C (36-86F), and has a shelf life of 12 to 24 months, as indicated on the product packaging. Proper storage ensures optimal performance and reliability of results.
Q: What are the key benefits of using the FIAflex cTnI FIA Test?
A: Key benefits include rapid results within 10-15 minutes, high clinical sensitivity, ease of use, portability, and the ability to operate in real-time at the point-of-care, supporting swift diagnostic decision-making in acute settings.
Tell us about your requirement
Price:
Quantity
Select Unit
50
100
200
250
500
1000+
Additional detail
Mobile number
Email
Name
Comapny Name
Phone Number
Email Id
City / State
Confirm Your Requirement
Verification Code
Did not receive yet?
Resend OTP
You’re Done!
We have received your requirements and will reply shortly with the best price.