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SUMO Protease is a recombinant form of Saccharomyces cerevisiae protease produced in Escherichia coli. SUMO protease can recognize the SUMO tertiary structure and cleave it, has high specificity, and there would be no amino acid residues. This product contains His-tag which can be removed by Ni2+ affinity chromatography resin.
Remove SUMO-tag in any recombinant SUMO fusion protein.
One unit of SUMO Protease cleaves ≥ 85% of 2 μg control substrate in 1 h at 30℃.
>95% as determined by SDS-PAGE.
>10 U/μL
Less than 0.2 EU per μg by the LAL method / rFC method.
Supplied as 0.2 μm filtered solution in 250 mM NaCl, pH 8.0 with glycerol as protectant.
Contact us for customized product form or formulation.
This product is supplied and shipped on dry ice.
*The 10× Reaction Buffer provided in this kit contains DTT, a sulfhydryl reducing agent essential for maintaining enzyme activity. When employing the 10× Reaction Buffer exposed to prolonged storage or repeated freeze-thaw cycles, fresh 10 mM DTT should be supplemented to the Reaction Buffer to ensure maximal enzymatic activity, as oxidative degradation of DTT progressively compromises its reducing capacity.