Cat# | Product Name | Price |
---|---|---|
Kit-0181 | Cathepsin B Activity Fluorometric Assay Kit | Inquiry |
Kit-0182 | Cathepsin D Activity Fluorometric Assay Kit | Inquiry |
Kit-0183 | Cathepsin G Activity Colorimetric Assay Kit | Inquiry |
Kit-0184 | Cathepsin K Activity Fluorometric Assay Kit | Inquiry |
Kit-0185 | Cathepsin K drug discovery Kit | Inquiry |
Kit-0186 | Cathepsin L Activity Fluorometric Assay Kit | Inquiry |
Kit-0187 | Cathepsin S Activity Fluorometric Assay Kit | Inquiry |
Kit-0188 | Cathepsin S drug discovery Kit | Inquiry |
Kit-2270 | Cathepsin H Activity Fluorometric Assay Kit | Inquiry |
Kit-2271 | Cathepsin B Activity Fluorometric Assay Kit II | Inquiry |
Cathepsins represent a group of lysosomal proteases, which constitute key players in protein turnover. These enzymes break apart the bonds of other proteins, effectively facilitating the ‘digest’ and ‘recycling’ process of proteins. In this way, the materials of damaged or unrequired proteins can be used to create new ones.
Cathepsin can be further categorized into several types, including Cathepsin B, D, and L, based on their specificity and preference for certain amino acids. While their standard job is to manage protein turnover, they also play crucial roles in many other biological events, including immune response, hormone secretion, bone remodeling, and cell apoptosis. In some pathologic conditions such as cancer, neurodegenerative diseases, and cardiovascular diseases, aberrant activities of Cathepsin have been observed, adding to its pathophysiological significance.
Given Cathepsin’s importance and its association with various diseases, effective detection of this enzyme and measurement of its activity are paramount for investigative and diagnostic purposes. Over the years, several Cathepsin detection methods have been developed, with each having its own principles.
One common method of Cathepsin detection is western blotting, a technique widely used in protein identification. Here, the Cathepsin proteins are separated with a technique known as SDS-PAGE and then transferred onto a solid membrane where they are bound by specific antibodies. These antibodies are eventually visualized - the strength of the signal is proportional to the amount of Cathepsin in the sample.
Fluorescence-based assays offer another effective technique for detection and measurement of Cathepsin activity. The principle of this method is based on the enzymatic cleavage of a specific substrate by Cathepsin to produce a fluorescent signal, which is proportionate to its concentration. The greater the signal, the more the Cathepsin.
Effective execution of these methods requires precise and reliable detection tools. Several Cathepsin assay kits have been developed to meet this demand with each promise of optimal results.
Prominent among them are the Cathepsin Assay Kits, which offer an effective fluorescence-based method for Cathepsin activity detection. Their kits detect and differentiate between the activities of various Cathepsin types. Similarly, the Human Cathepsin ELISA Kits use the enzyme-linked immunosorbent assay method for the detection and measurement of different forms of Cathepsin in human serum, plasma, tissue homogenates, and other biological fluids.
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