TRAK1 Polyclonal Antibody, 20ul Pathway and Network Analysis Mutations in this gene cause

Mutations in this gene cause cerebellar ataxia in humans

Has no phosphatase 2A (PP2A) inhibitor activity (By similarity)

The amino acid sequence of this isozyme is 92% identical to that of rat homolog

Take your cell cultures to new heights with MetaCell®CHO-200 Medium

Certifications: The DLAB pipette has ISO9001:2015 and ISO 13485:2016 certifications

TRAK1 Polyclonal Antibody, 20ul Pathway and Network Analysis Mutations in this gene causePTM: O glycosylated.,Contains 1 HAP1 N terminal domain.,subunit: Interacts with O GlcNAc transferase. Interacts with RHOT1 Miro 1 and RHOT2 Miro 2.,tissue specificity: High expression in spinal cord and moderate expression in all other tissues and specific brain regions examined. Expressed in all cell lines examined.,