The TXA2 (Thromboxane A2) ELISA Kit is specifically designed for the accurate and precise detection of Thromboxane A2 levels in various biological samples such as serum, plasma, and tissue homogenates. With its high sensitivity and specificity, this kit offers reliable and reproducible results for researchers in the field of inflammation, thrombosis, and cardiovascular diseases.Thromboxane A2 is a key mediator in platelet aggregation and vasoconstriction, playing a critical role in various physiological and pathological processes. Dysregulation of TXA2 levels has been implicated in conditions such as atherosclerosis, stroke, and myocardial infarction, making it a valuable biomarker for studying these diseases and potential therapeutic interventions.Overall, the TXA2 ELISA Kit provides researchers with a powerful tool to study the role of Thromboxane A2 in health and disease, offering a comprehensive solution for quantitative analysis in both basic research and clinical applications.
Product Name:
TXA2 (Thromboxane A2) ELISA Kit
SKU:
UNES00037
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Competitive
Assay type:
Competitive-ELISA
Assay time:
2 h 30 min
Sensitivity:
9.38 pg/mL
Detection range:
15.63-1000 pg/mL
Reovery:
80%-120%
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with the target antigen. Standards or samples are added along with a biotinylated detection antibody. The target antigen present in the sample competes with the immobilized antigen for binding to the detection antibody. After incubation, Avidin-Horseradish Peroxidase (HRP) conjugate is added. Free components are washed away. The substrate solution is then added, resulting in a color change. The intensity of the color is inversely proportional to the concentration of the target antigen in the sample. The reaction is stopped by the addition of stop solution, and the color changes from blue to yellow. The optical density (OD) is measured at 450 nm ± 2 nm. The concentration of the target protein is calculated by comparing the OD values of the samples to the standard curve.
