NMRL1 Rabbit Polyclonal Antibody, 100ul Molecular Sciences Mutations in OCRL cause oculocerebrorenal

Mutations in OCRL cause oculocerebrorenal syndrome of Lowe and also Dent disease

required for the functional interaction of kinesin I with axonal cargo

This gene encodes a CXC chemokine receptor specific for stromal cell-derived factor-1

3 ubiquitin-protein ligase

HGFAC encodes a member of the peptidase S1 protein family

NMRL1 Rabbit Polyclonal Antibody, 100ul Molecular Sciences Mutations in OCRL cause oculocerebrorenalThis gene encodes an NADPH sensor protein that preferentially binds to NADPH. The encoded protein also negatively regulates the activity of NF kappaB in a ubiquitylation dependent manner. It plays a key role in cellular antiviral response by negatively regulating the interferon response factor 3 mediated expression of interferon beta. Alternative splicing of this gene results in multiple transcript variants.