Recombinant Human HSP22 - 10 μg

Hsp22, a Mn+2-dependent serine-threonine-specific protein kinase, displays temperaturedependent chaperone activity. Defects in Hsp22 cause distal hereditary motor neuropathy type 2 (also known as distal spinal muscular atrophy) and spinal muscular atrophy of the charcot-marietooth type.

Product Specifications

Target

Hsp22

Applications

Shipping Conditions

Next Day 2-8°C

Storage Conditions

Although stable at room temperature for 3 weeks, should be stored desiccated below -18°C. Upon reconstitution, product should be stored at 4°C between 2-7 days and for future use below -18°C. Addition of a carrier protein (such as 0.1% HSA or BSA) is recommended for long-term storage. Avoid multiple freeze-thaw cycles.

Formulation

Lyophilized from a 1mg/ml sterile-filtered solution in 20mM Tris-acetate buffer, pH 7.6, 10mM NaCl, 0.1mM EDTA, 0.1mM PMSF, and 15mM β-mercaptoethanol.