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

an autosomal recessive disorder with cerebellar hypoplasia as a leading feature

PTM:Serine or threonine phosphorylation within the basic region may regulate neurogenic activity

Binds G/C-rich sites via its zinc fingers and activates transcription from CACCC-box elements

This gene encodes a replication-independent histone that is a member of the histone H1 family

A related pseudogene has also been identified approximately 75 kb downstream of this gene on chromosome X

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