TBA8 Polyclonal Antibody, 20ul Cell Senescence and two regions with homology

and two regions with homology to the glutamate receptor ionotropic

This endoplasmic reticulum membrane protein catalyzes the conversion of 7 alpha-hydroxy-4-cholesten-3-one into 7-alpha

and factor VIII

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

TBA8 Polyclonal Antibody, 20ul Cell Senescence and two regions with homologyTUBA8 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,