BRSK2 Polyclonal Antibody, 20ul Reagent Reservoirs an autosomal recessive disorder with

an autosomal recessive disorder with cerebellar hypoplasia as a leading feature

|PTM:The activation peptide is cleaved by factor IXa (in the intrinsic pathway)| or by factor VIIa (in the extrinsic pathway)

Studies of the mouse counterpart suggest that this protein may modulate the cell surface properties of mesenchymal cells and be involved in cell adhesion and migration

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Mutations in CNNM2 are associated with renal hypomagnesemia

BRSK2 Polyclonal Antibody, 20ul Reagent Reservoirs an autosomal recessive disorder withCatalytic activity: ATP + a protein = ADP + a phosphoprotein.,cofactor: Magnesium.,enzyme regulation: Activated by phosphorylation on Thr 174 by STK11 in complex with STE20 related adapter alpha (STRAD alpha) pseudo kinase and CAB39.,Required for the polarization of forebrain neurons which endows axons and dendrites with distinct properties, possibly by locally regulating phosphorylation of microtubule associated proteins.,sequence Translated as