Glutathione S-transferase (GST) is a 26 kDa protein derived from Schistosoma japonicum. GST enzymes from various sources, both native and recombinantly expressed as fusion to the N-terminus of target proteins, are easily purified in a one-step procedure by affinity chromatography on immobilized glutathione (Glutathione Agarose, Fast Flow).

Due to the positive influence of the GST-tag on protein solubility and expression efficiency especially of small proteins, this technique has been widely used to generate proteins for crystallization, molecular immunology studies and studies involving protein-protein and protein-DNA interactions.

However, the comparably large GST-tag might sometimes interfere with these downstream applications. In these cases it is easily removed by protease cleavage e.g. by Factor Xa provided that a specific protease sequence is located between the protein domain and GST.
 

Glutathione Magnetic Agarose Beads

Ferrimagnetic agarose beads suitable for fast & efficient small-scale purification of GST and GST tagged proteins.
 

Glutathione Agarose, Fast Flow

High-performance 4 % agarose suitable for FPLC, gravity flow and batch purification of GST and GST tagged proteins.