BRSK2 Polyclonal Antibody, 50ul Mechanical Pipette Mutations in this gene cause

Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA)

Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease

including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM)

Nitric oxide-sensitive guanylyl cyclase is a heterodimeric enzyme consisting of an alpha and a beta subunit

SPOP (speckle type BTB/POZ protein) encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX)

BRSK2 Polyclonal Antibody, 50ul Mechanical Pipette Mutations in this gene causeCatalytic 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