Rat cTnT/TNNT2 (Troponin T Type 2, Cardiac) ELISA Kit
The Rat cTnT/TNNT2 (Troponin T Type 2, Cardiac) ELISA Kit is meticulously designed for the precise quantitative detection of Troponin T Type 2 levels in various biological samples. Troponin T Type 2, a specific marker of cardiac injury, is crucial in the diagnosis and assessment of cardiac conditions, particularly myocardial infarction and myocardial damage. Elevated levels of cTnT are indicative of cardiac muscle damage, making it an essential biomarker in cardiology research and clinical practice. Accurate measurement of cTnT/TNNT2 is paramount for early diagnosis of cardiac pathologies, monitoring treatment efficacy, and predicting patient outcomes. This ELISA kit offers exceptional sensitivity and specificity, ensuring reliable and reproducible results. Manufactured under strict quality control measures, the kit guarantees robust performance and user-friendly operation, making it an ideal choice for cardiovascular research and diagnostic applications.
Product Name:
Rat cTnT/TNNT2 (Troponin T Type 2, Cardiac) ELISA Kit
SKU:
AEES00340
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.
