MMP-2 (Mouse) ELISA Kit

Kits

貨號 Cat. No.
E4725-100
規格 Size
E4725-100
Reactivity
Mouse
Sample Type
Other biological fluids 、 Plasma 、 Serum

Description




Alternate Name : MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1, Gelatinase A, Matrix Metalloproteinase 2


 

Tag Line :


A sandwich ELISA kit for in vitro quantitative determination of mouse MMP-2 concentrations in serum, plasma and other biological fluids.


 

Storage Conditions: 4ºC


 

Shelf life: 6 months


 

Summary :



 

Detection Method: Absorbance (450 nm)


 

Features & Benefits:


Specificity: This kit recognizes Mouse MMP-2 in samples. No Significant cross-reactivity or interference between Mouse MMP-2 and analogues was observed., Detection Range:0.16 - 10 ng/ml, Sensitivity: 0.10 ng/ml, Coefficient of variation is < 10%


 

Description:


The mammalian Matrix metalloproteinases (MMPs) degrade extracellular matrix in physiological and pathological processes. After cleavage of a single peptide domain of about 20 amino acids, the MMPs are secreted in latent forms. Upon activation, the N-terminal propeptide domain is cleaved to generate the active forms of MMP. MMP-2 (72 kDa type IV collagenase, Gelatinase-A) contains the basic structure of propeptide, catalytic, and hemopexin domains. It is an important proteinase in tissue remodeling. BioVision’s MMP-2 ELISA kit is based on the Sandwich-ELISA principle. The micro ELISA plate provided in the kit has been pre-coated with an antibody specific to mouse MMP-2. On addition of standards or samples to the micro ELISA plate, they react with Biotinylated detection antibody specific for mouse MMP-2 and Avidin-Horseradish Peroxidase (HRP) conjugate, which on the addition of substrate gives blue color. The enzyme-substrate reaction is terminated by the addition of stop solution to turn the reaction yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of mouse MMP-2.The concentration of Mouse MMP-2 in the samples was calculated by comparing the OD of the samples to the standard curve.


 





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