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Rho-associated protein kinase 2 (ROCK2) is a serine/threonine kinase that has roles in cytoskeletal organization and autoimmunity, as well as cell survival, proliferation, and apoptosis.1,2,3 It exists as a homodimer where each monomer is composed of an N-terminal kinase domain, a coiled-coil region that contains the Rho-binding domain, and a C-terminal pleckstrin homology (PH) domain that contains a cysteine-rich C1 domain and acts as an autoinhibitory region.4,2 Rock2 mRNA is expressed in brain, muscle, heart, lung, and placenta, localized to the cytosol and nucleus, associated with the centrosome, and co-localized with actin and vimentin in a cell-type-specific manner.1,2 Binding of ROCK2 to GTP-bound RhoA induces activation of ROCK1, which phosphorylates a variety of downstream targets, including myosin light chain (MLC) phosphatase 1 (MYPT1) and MLC2, that have diverse roles in cytoskeletal organization.2 Additionally, ROCK2 is cleaved and activated by proteases, including granzyme B and caspase-2, to induce apoptosis.1 Pharmacological inhibition of ROCK2 restores immune homeostasis and shifts the helper T (Th17)/regulatory T (Treg) cell balance towards Tregs in various animal models of autoimmunity and chronic graft versus host disease (GVHD).3 Rock2 knockdown decreases the fibrogenic response in a mouse model of diabetic kidney disease.5 Cayman's ROCK2 (human, recombinant) protein can be used for enzyme activity assays.
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1. The function of Rho-
2. Rho-
3. ROCK2, a critical regulator of immune modulation and fibrosis has emerged as a therapeutic target in chronic graft-
4. RhoBTB1 interacts with ROCKs and inhibits invasion. Biochem. J. 476(17), 2499-2514 (2019).
5. The physiology, pathology, and therapeutic interventions for ROCK isoforms in diabetic kidney disease. Front. Pharmacol. 11, 585633 (2020).