Beta-tubulin (HRP Conjugated) Monoclonal Antibody(5G3), 100ul Isothermal Amplification Mutations in this gene cause

Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease

and may play additional roles in nucleo-cytoplasmic shuttling

RUNX3 encodes a member of the runt domain-containing family of transcription factors

IV and III are shorter

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Beta-tubulin (HRP Conjugated) Monoclonal Antibody(5G3), 100ul Isothermal Amplification Mutations in this gene causeThis gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13.