Human cTnT/TNNT2 (Troponin T Type 2, Cardiac) ELISA Kit
The Human cTnT (Troponin T Type 2) Cardiac ELISA Kit is specially designed for the precise measurement of cTnT levels in human samples such as serum, plasma, and cell culture supernatants. This ELISA kit offers superior sensitivity and specificity, ensuring accurate and consistent results for various research purposes.cTnT is a key cardiac marker indicative of myocardial injury and is commonly used in the diagnosis and monitoring of acute coronary syndromes. Elevated cTnT levels are associated with heart conditions such as myocardial infarction and heart failure, underscoring its importance in clinical research and patient care. With this advanced ELISA kit, researchers can analyze cTnT levels with confidence, enabling them to better understand cardiac health and develop more effective treatments for cardiovascular diseases. Trust in the Human cTnT Cardiac ELISA Kit for reliable and insightful results in your cardiac research endeavors.
Product Name:
Human cTnT/TNNT2 (Troponin T Type 2, Cardiac) ELISA Kit
SKU:
HUES01807
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
9.38 pg/mL
Detection range:
15.63-1000 pg/mL
Reovery:
80%-120%
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to the target protein. Standards or samples are added to the micro ELISA plate wells and bind to the immobilized antibody. A biotinylated detection antibody specific to the target protein is then added, followed by Avidin-Horseradish Peroxidase (HRP) conjugate. Free components are washed away. The substrate solution is added to each well, resulting in a color change. Only wells containing the target protein, detection antibody, and HRP conjugate will develop a blue color. The reaction is terminated by the addition of stop solution, resulting in a yellow color. The optical density (OD) is measured at 450 nm ± 2 nm. The OD value is directly proportional to the concentration of the target protein in the sample and is determined using a standard curve.
