BRSK2 Polyclonal Antibody, 50ul Mechanical Pipette MIM 610611)

MIM 610611)

Mutations in this gene have been linked with Li-Fraumeni syndrome

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

act as molecular switches that play crucial roles in the regulation of fundamental cellular processes such as protein synthesis

BRSK2 Polyclonal Antibody, 50ul Mechanical Pipette MIM 610611)Catalytic 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