HSP90Beta Monoclonal Antibody(M2), 100ul Protein Post-translational Modification This gene is located between

This gene is located between the Charcot-Marie-Tooth and Smith-Magenis syndrome critical regions on chromosome 17

and are a major causative factor in the neurological symptoms of 22q13

|After shedding| the soluble form (sCD163) may play an anti-inflammatory role| and may be a valuable diagnostic parameter for monitoring macrophage activation in inflammatory conditions

An important paralog of this gene is FOXE3

The protein encoded by this gene belongs to the glutathione peroxidase family| members of which catalyze the reduction of hydrogen peroxide| organic hydroperoxides and lipid hydroperoxides| and thereby protect cells against oxidative damage

HSP90Beta Monoclonal Antibody(M2), 100ul Protein Post-translational Modification This gene is located betweenThis gene encodes a member of the heat shock protein 90 family these proteins are involved in signal transduction, protein folding and degradation and morphological evolution. This gene encodes the constitutive form of the cytosolic 90 kDa heat shock protein and is thought to play a role in gastric apoptosis and inflammation. Alternative splicing results in multiple transcript variants. Pseudogenes have been identified on multiple chromosomes.