Human MMP-10 (Matrix Metalloproteinase 10) ELISA Kit
The Matrix Metalloproteinase 10 (MMP-10) ELISA Kit is meticulously developed for the precise quantitative analysis of MMP-10 levels in various human samples. MMP-10, an important member of the MMP family of enzymes, plays a key role in extracellular matrix remodeling and tissue homeostasis. As a biomarker of tissue remodeling and inflammation, MMP-10 is implicated in various pathological processes, including cancer progression, cardiovascular diseases, and tissue repair mechanisms. This ELISA kit ensures exceptional sensitivity and specificity, enabling the accurate and reproducible measurement of MMP-10 levels. Manufactured under strict quality control procedures, the kit delivers robust and reliable performance while being user-friendly. Count on Assay Genie's MMP-10 ELISA Kit for precise and consistent quantification of this critical biomarker in your research and clinical investigations.
Product Name:
Human MMP-10 (Matrix Metalloproteinase 10) ELISA Kit
SKU:
AEES00058
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.
