Tubulin Beta Polyclonal Antibody, 100ul Recombinant Protein Defects in this gene are

Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59)

The protein encoded by this gene is a calcium-dependent glycoprotein that is a member of the desmocollin subfamily of the cadherin superfamily

It is noteworthy that this gene and LEPROT gene (GeneID: 54741) share the same promoter and the first 2 exons

The encoded protein is likely involved in neurite branching

It is a minor species carried by human erythrocytes

Tubulin Beta Polyclonal Antibody, 100ul Recombinant Protein Defects in this gene areTUBB3 encodes a class III member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. Tubulin beta 3 chain is primarily expressed in neurons and may be involved in neurogenesis and axon guidance and maintenance. Mutations in this gene are the cause of congenital fibrosis of the extraocular muscles type 3. Alternate splicing results in