Cell Culture Reagents

Cathepsin B is a lysosomal enzyme that comprises a light chain (Lys1–Arg49) and a heavy chain (Val50–Thr253). It belongs to cysteine family C1.

Cathepsin B is a lysosomal enzyme that comprises a light chain (Lys1–Arg49) and a heavy chain (Val50–Thr253). It belongs to cysteine family C1.

Cell Dilution Buffer II

Cell Dissociation Solution Non-enzymatic buffer systems are alternative to the canonical trypsin based buffers for dissociation of adherent mesenchymal stem cell (MSC) monolayers. Application Cell Dissociation Solution Non-enzymatic 1x has been

Cell dissociation by non-enzymatic methods in human mesenchymal stromal cells aid in their detachment and preserves their functionality especially the expression of cell surface chemokine receptor. Application Cell Dissociation Solution

The Cell Proliferation Labeling Reagent is an aqueous solution of 5-bromo-2-deoxyuridine and 5-fluoro-2′-deoxyuridine and allows extended use of the Cell Proliferation Kit when additional amounts of labeling reagent are required. Application The

Contents Ready-to-use solution, containing WST-1 and an electron coupling reagent. Cellular proliferation requires the replication of genomic DNA.

Introducing the new High-Yielding Performance Flask Manual (HYPERFlask M) cell culture vessel. The HYPERFlask M vessel is specifically designed for manual use.

Introducing the new High-Yielding Performance Flask Manual (HYPERFlask M) cell culture vessel. The HYPERFlask M vessel is specifically designed for manual use.

Introducing the new High-Yielding Performance Flask Manual (HYPERFlask M) cell culture vessel. The HYPERFlask M vessel is specifically designed for manual use.

Cellvento &#174 4CHO-C Cloning Medium supports CHOZN &#174 and CHO cell line development and has been developed to replace hydrolysate containing EX-CELL &#174 CHO Cloning Medium (C6366) at comparable performance. It provides chemically defined

Application A proprietary, non-denaturing formulation of zwitterionic detergents used for the lysis of bacterial cells and extraction of recombinant proteins. Features and Benefits Higher protein extraction efficiency than traditional methods such