Human Cyr61 (Cysteine Rich Protein, Angiogenic Inducer 61) ELISA Kit
The Human CYR61 (Cysteine-rich protein 61) ELISA Kit is specifically designed for the accurate detection of CYR61 levels in human serum, plasma, and cell culture supernatants. This kit offers high sensitivity and specificity, ensuring reliable and reproducible results for a variety of research applications.CYR61 is a key protein known for its role as an angiogenic inducer, promoting angiogenesis and influencing various cellular processes. Its involvement in conditions such as cancer, cardiovascular diseases, and neurodegenerative disorders makes it a valuable biomarker for studying these diseases and developing potential therapeutic interventions. With the Human CYR61 ELISA Kit, researchers can effectively measure CYR61 levels in biological samples, gaining valuable insights into its role in health and disease. This kit is a valuable tool for advancing research in the field of angiogenesis and related conditions.
Product Name:
Human Cyr61 (Cysteine Rich Protein, Angiogenic Inducer 61) ELISA Kit
SKU:
HUES02342
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
18.75 pg/mL
Detection range:
31.25-2000 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.
