Shank 2 Polyclonal Antibody, 50ul Gloves Mutations in EPHA2 are the

Mutations in EPHA2 are the cause of certain genetically-related cataract disorders

DNAJ family members are characterized by a highly conserved amino acid stretch called the 'J-domain' and function as one of the two major classes of molecular chaperones involved in a wide range of cellular events

a single pass transmembrane region

CD6 may be associated with susceptibility to multiple sclerosis (PMID: 19525953

Shank 2 Polyclonal Antibody, 50ul Gloves Mutations in EPHA2 are theSHANK2 encodes a protein that is a member of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses. Shank proteins contain multiple domains for protein protein interaction, including ankyrin repeats, and an SH3 domain. This particular family member contains a PDZ domain, a consensus sequence for cortactin SH3 domain binding peptides and a sterile alpha motif. The alternative