【PERFORMANCE CHARACTERISTICS】 1. Accuracy The test deviation is ≤±15%. 2. Sensitivity The H-FABP Test Cassette can detect levels of H-FABP as low as 1ng/ml in whole blood, serum or plasma. 3. Detection range 1-120ng/ml 4. Linearity range 1-120ng/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) |
Diagnostic FABP Test Use By Citest GO fluorescence Immunoassay Analyzer In Human whole blood /serum /plasma
A test for measuring FABP in whole blood /serum /plasma with the use of Citest TM Go fluorescence Immunoassay Analyzer. For professional in vitro diagnostic use only.
Application And Description:
FABP is a newly introduced plasma marker of acute myocardial infarction (AMI). The plasma kinetics of FABP (15kD) closely resemble those of H-FABP in that elevated plasma concentrations are found within 2 hours after AMI and return to normal generally within 18 to 24 hours. But the concentration of FABP in the skeletal muscle is 20 times lower than in cardiac tissue (for H-FABP the same content for cardiac and skeletal tissue), that makes FABP to be more cardiac specific than H-FABP. This makes FABP a useful biochemical marker for the early assessment or exclusion of AMI.
FABP also appears to be a useful plasma marker for the estimation of myocardial infarct size. FABP is suitable for use as a standard in immunoassay for early detection of acute myocardial infarction, immunogen for antisera production, mass FABP standard, FABP biochemical and immunochemical studies, tracer for iodination.
Principle | Fluorescence Immunoassay |
Format | Cassette |
Specimen | WB/S/P |
Certificate | CE |
Reading Time | 15 minutes |
Pack | 10T/25T |
Storage Temperature | 4-30℃ |
Shelf Life | 2 Years |
Cut-Off | 8ng/mL |
How to use?
Refer to Citest TM Go Fluorescence Immunoassay Analyzer Operation Manual for the complete instructions on use of the Test. The test should be conducted in 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: Pipette 50μL serum/plasma into the buffer tube, mix the specimen and the buffer well.
4. Whole blood: Transfer 75μL whole blood into the buffer tube with pipette; mix the specimen and the buffer well.
5. Add diluted specimen with a Pipette: Pipette 85μL diluted specimen into the sample well of the test cassette. Start the timer at the same time.
6. There are two test modes for Citest TM Go Fluorescence Immunoassay Analyzer, Standard Test mode and Quick Test mode.
Please refer to the user manual of Citest TM Go Fluorescence Immunoassay Analyzer for details.
“Quick test” mode: After 15 minutes of adding sample,Insert the test cassette into the Analyzer, click “QUICK TEST”, fill the test information and click "NEW TEST" immediately. The Analyzer will automatically give the test result after a few seconds.
“Standard test” mode: Insert the test cassette into the Analyzer immediately after adding specimen, click “STANDARD TEST”, fill the test information and click "NEW TEST" at the same time, The Analyzer will automatically countdown 15 minutes. After the countdown, the Analyzer will give the result at once.
The H-FABP Test Cassette is based on Fluorescence Immunoassay to measure H-FABP in whole blood or plasma as an aid in the diagnosis of acute myocardial infarction (AMI).The test result is calculated by Fluorescence Immunoassay Analyzer.
Catalogue Number | Item Name | Sample | Test Range | KIT size |
FI-HFA-402 | H-FABP Test Cassette | WB/S/P | 1-120 ng/mL | 10T/25 |