NPM(Phospho-Thr95) Rabbit Polyclonal Antibody, 50ul Cell Proliferation Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level

1 and perfect for MX-S and MX-F Vortex Mixers

This protein is one of the entry cofactors for hepatitis C virus

Extensive alternative splicing produces isoforms with different C-termini that are proposed to bind to different cargos

NPM(Phospho-Thr95) Rabbit Polyclonal Antibody, 50ul Cell Proliferation Defects in TMEM237 are aThis gene encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF p53 pathway. A number of genes are fusion partners have been characterized in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in this gene are associated with acute myeloid leukemia. More than a dozen pseudogenes of this gene have been identified.