Mouse TNNI3/cTn-I (Troponin I Type 3, Cardiac) ELISA Kit
The Mouse cTnI (Troponin I, Cardiac) ELISA Kit is specifically designed for the quantitative measurement of cardiac troponin I type 3 levels in mouse samples, including serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring accurate and reliable results for a variety of research applications.cTnI is a crucial protein involved in cardiac muscle function, serving as a biomarker for myocardial injury and a key indicator of cardiac health. Elevated levels of cTnI are associated with conditions such as myocardial infarction, heart failure, and cardiac arrhythmias, making this kit essential for studying these conditions and developing potential therapeutic interventions.With precise and consistent results, the Mouse cTnI ELISA Kit is a valuable tool for researchers studying cardiovascular diseases and seeking to understand the mechanisms underlying cardiac muscle function.
Product Name:
Mouse TNNI3/cTn-I (Troponin I Type 3, Cardiac) ELISA Kit
SKU:
MOES01590
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
4.69 pg/mL
Detection range:
7.81-500 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.
