MAP3K2 Rabbit Polyclonal Antibody, 100ul Proteases Mutations in this gene are

Mutations in this gene are the cause of congenital fibrosis of the extraocular muscles type 3

similarity:Belongs to the major facilitator superfamily

Has no activity towards aliphatic aldehydes and ketones

Beta-adrenergic receptor kinase 1 phosphorylates the beta-2-adrenergic receptor and appears to mediate agonist-specific desensitization observed at high agonist concentrations

A domain at its N-terminus can also interact with the poly(A)-binding protein

MAP3K2 Rabbit Polyclonal Antibody, 100ul Proteases Mutations in this gene areThe protein encoded by this gene is a member of serine threonine protein kinase family. This kinase preferentially activates other kinases involved in the MAP kinase signaling pathway. This kinase has been shown to directly phosphorylate and activate Ikappa B kinases and thus plays a role in NF kappa B signaling pathway. This kinase has also been found to bind and activate protein kinase C related kinase 2 which suggests its involvement in a regulated