切换导航

Cathepsin K Activity Fluorometric Assay Kit

现货
Catalog No.
K2152
检测组织蛋白酶K活性,敏感。
组合的产品项目
规格价格库存 数量
100 assays
¥ 4,020.00
Ship with 10-15 days

电话: 021-55669583

邮箱: sales@apexbio.cn

全球经销商

Background

Apoptosis is often mediated by the traditional caspase-mediated cleavage cascade. In addition, alternative proteolytic enzymes such as the lysosomal cathepsin proteases can also initiate or propagate proapoptotic signals. Cathepsins are lysosomal proteases that play an important role in mammalian cellular turnover such as bone resorption. Cathepsins are often used as sensitive markers in a variety of toxicological investigations. Cathepsin K is an lysosomal cysteine protease belonging to the peptidase C1 family. Cathepsin K is expressed predominantly in osteoclasts and is involved in bone remodeling and resorption. Cathepsin K is stimulated by inflammatory cytokines that are released after tissue injury. The Cathepsin K Activity Fluorometric Assay Kit provides a sensitive, simple and convenient way for detection of cathepsin K activity based on fluorometric method. The assay utilizes the preferred cathepsin-K substrate sequence LR labeled with AFC (amino-4-trifluoromethyl coumarin). While cleavage of the synthetic substrate LR-AFC by cathepsin-K in cell lysates or other samples, free AFC emits a yellow-green fluorescence (λmax = 505 nm) that can be easily quantified using a fluorecence microtiter plate reader or a fluorometer.

Features & Properties

FeaturesFast and convenient. Simple one-step procedure; takes only 1-2 hours. Cathepsin-K assay is straightforward, and can be adapted to 96-well plate assays.
ShippingGel pack
Storage ConditionsStore at -20℃.

质量控制

Quality Control & DataSheet

View current batch:
 

Overview

Species reactivityMammalian
ApplicationsDetects alternative proteolytic enzymes such as the lysosomal cathepsin proteases that can initiate or propagate proapoptotic signals.
Kit componentsCK Cell Lysis Buffer CK Reaction Buffer CK Substrate Ac-LR-AFC (10 mM) CK Inhibitor (1 mM)

Structure

no_selection