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Myocardial infarction test kit DR1039
β-hCGcardiac troponin ID-dimer

Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 2
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 3
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 4
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 5
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 6
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 7
Myocardial infarction test kit - DR1039 - Jiangsu Zecen Biotech Co., Ltd - β-hCG / cardiac troponin I / D-dimer - image - 8
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Characteristics

Applications
for myocardial infarction
Tested parameter
D-dimer, cardiac troponin I, NT-proBNP, h-FABP, for cTnT, β-hCG
Sample type
clinical, blood
Analysis mode
CLIA

Description

The kit has been designed for the quantitative determination of N-terminal pro-Brain Natriuretic Peptide (NT-proBNP) in human serum. The method can be used for samples over the range of 15-16000 pg/mL. PRINCIPLE OF THE TEST: Sandwich method: NT-proBNP antibody labeled by FITC and NT-proBNP Antibody pair labeled by AP bind with the NT-proBNP antigen in the sample, control or calibrator and form sandwich complex. Then add the magnetic beads binding with Anti-FITC, through the specific binding between the FITC and Anti-FITC, the complex will be bound by the magnetic beads. Then the entire complex will be captured by the external applied magnetic field and separate from the unbound substance. After washing, add the substrate. The substrate will be catalytically cracked under the action of the enzyme, and form an unstable intermediate in excited state. When the intermediate in excited state returns to the ground state, it will issue photons and make a light-emitting reaction. Then the CLIA analyzer will measure the luminous intensity and count the results through software by comparing the luminous intensity with the cutoff value to determine whether the corresponding antibody exists. DESCRIPTION: Specification - 100 test/kit 50 test/kit 48 test/kit Principle - Sandwich Method Components - Magnetic beads Anti-A/Anti-B Calibrators QC 1 QC 2 Sample - Serum

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