Smad5 Monoclonal Antibody, 100ul[BT-MCA1138] 3D Culture this proteolipid is localized in

this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function

NCLN (Nicalin) is a Protein Coding gene

Mutations in this gene are a cause of spastic ataxia 2| autosomal recessive

The enzyme encoded by this gene lacks a C-terminal TS motif

This gene encodes a member of the ETS (E twenty-six) family of transcription factors

Smad5 Monoclonal Antibody, 100ul[BT-MCA1138] 3D Culture this proteolipid is localized inThe protein encoded by this gene is involved in the transforming growth factor beta signaling pathway that results in an inhibition of the proliferation of hematopoietic progenitor cells. The encoded protein is activated by bone morphogenetic proteins type 1 receptor kinase, and may be involved in cancer. Alternative splicing results in multiple transcript variants.