TBA8 Polyclonal Antibody, 20ul Cell Senescence Mutations in this gene cause

Mutations in this gene cause spinocerebellar ataxia type 15| a disease associated with an heterogeneous group of cerebellar disorders

These proteins are secreted ligands of leucine-rich repeat containing G protein-coupled receptors that enhance Wnt signaling through the inhibition of ubiquitin E3 ligases

This gene encodes a protein containing multiple zinc finger domains

c-fos promoters and several enhancers

and factor VIII

TBA8 Polyclonal Antibody, 20ul Cell Senescence Mutations in this gene causeTUBA8 encodes a member of the alpha tubulin protein family. Alpha tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. Mutations in this gene are associated with polymicrogyria and optic nerve hypoplasia. Alternate splicing results in multiple transcript variants. TUBA8 (Tubulin Alpha 8) is a Protein Coding gene. Diseases associated with TUBA8 include Cortical Dysplasia,