Myocardial infarction test kit CFA-402
h-FABPserumplasma

myocardial infarction test kit
myocardial infarction test kit
myocardial infarction test kit
myocardial infarction test kit
myocardial infarction test kit
myocardial infarction test kit
myocardial infarction test kit
myocardial infarction test kit
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Characteristics

Applications
for myocardial infarction
Tested parameter
h-FABP
Sample type
serum, plasma, whole blood
Analysis mode
immunoassay
Result display time

10 min

Description

Heart Fatty Acid-Binding Protein (h-FABP) Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid visual immunoassay for the qualitative presumptive detection of h-FABP in human whole blood, serum, or plasma specimens. This kit is intended to be used as an aid in the diagnosis of myocardial infarction (MI). Intend to use Heart-type fatty acid binding protein (h-FABP) is known as mammary-derived growth inhibitor is a protein that in humans is encoded by the FABP3 gene. Heart-type Fatty Acid-Binding Protein (H-FABP) is a small cytoplasmic protein (15 kDa) released from cardiac myocytes following an ischemic episode. Like the nine other distinct FABPs that have been identified, H-FABP is involved in active fatty acid metabolism where it transports fatty acids from the cell membrane to mitochondria for oxidation. h-FABP is a sensitive biomarker for myocardial infarction and can be detected in the blood within one to three hours of the pain. The diagnostic potential of the biomarker H-FABP for heart injury was discovered in 1988 by Professor Jan Glatz (Maastricht, Netherlands) h-FABP is 20 times more specific to cardiac muscle than myoglobin, it is found at 10-fold lower levels in skeletal muscle than heart muscle and the amounts in the kidney, liver and small intestine are even lower again. Operating StepsHealthcare pregnant diagnostic ffn Rapid test kit Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use. 1) Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour.

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