NRN1 Polyclonal Antibody, 100ul Lentiviral Packaging Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

RAD50 double strand break repair protein complex binds to DNA and displays numerous enzymatic activities that are required for nonhomologous joining of DNA ends

Sterilized and non-sterilized versions are available

thereby regulating imprinted expression

such as RAB1B (RAB1B

NRN1 Polyclonal Antibody, 100ul Lentiviral Packaging Mutations in this gene areThis gene encodes a member of the neuritin family, and is expressed in postmitotic differentiating neurons of the developmental nervous system and neuronal structures associated with plasticity in the adult. The expression of this gene can be induced by neural activity and neurotrophins. The encoded protein contains a consensus cleavage signal found in glycosylphoshatidylinositol (GPI) anchored proteins. The encoded protein promotes neurite outgrowth