Stathmin-3 Polyclonal Antibody, 20ul Cell Separation and Collection Mutations in this gene have

Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency)

neurodegenerative disorders affecting children

Serine/threonine-protein kinase MARK1 involved in cell polarity and microtubule dynamics regulation

The inner- and outer-arm dyneins

It is regulated by specific stimulatory events

Stathmin-3 Polyclonal Antibody, 20ul Cell Separation and Collection Mutations in this gene haveSTMN3 encodes Stathmin 3 which is a member of the stathmin protein family. Members of this protein family form a complex with tubulins at a ratio of 2 tubulins for each stathmin protein. Microtubules require the ordered assembly of alpha and beta tubulins, and formation of a complex with stathmin disrupts microtubule formation and function. A pseudogene of this gene is located on chromosome 22. Alternative splicing results in multiple transcript