TCPR2 Rabbit Polyclonal Antibody, 100ul Mammalian Expression is an autosomal dominant neurologic

is an autosomal dominant neurologic disorder

This gene encodes a member of the basic-leucine zipper family and the AMP-dependent transcription factor family

ay play a role in T-cell development

influence the spatial distribution of microtubules within cells and utilize microtubule polarity to translocate cellular components

It is a type I integral membrane protein with a heavily glycosylated extracellular domain and binds to tissue- and organ-specific lectins or selectins

TCPR2 Rabbit Polyclonal Antibody, 100ul Mammalian Expression is an autosomal dominant neurologicThe protein encoded by this gene is a member of the tectonin beta propeller repeat containing (TECPR) family and contains both TECPR and tryptophan aspartic acid repeat (WD repeat) domains. This gene has been implicated in autophagy as reduced expression levels of this gene have been associated with impaired autophagy. Recessive mutations in this gene have been associated with a hereditary form of spastic paraparesis (HSP). HSP is characterized by