SC22C Rabbit Polyclonal Antibody, 20ul Cell Separation and Collection Mutations in FMN2 have been

Mutations in FMN2 have been associated with mental retardation autosomal recessive 47 (MRT47)

It is associated with islet cell regeneration and diabetogenesis and may be involved in pancreatic lithogenesis

Several alternatively spliced transcript variants of DMPK have been described

GRO-beta(5-73) shows a highly enhanced hematopoietic activity

SC22C Rabbit Polyclonal Antibody, 20ul Cell Separation and Collection Mutations in FMN2 have beenThis gene encodes a member of the SEC22 family of vesicle trafficking proteins. The encoded protein is localized to the endoplasmic reticulum and may play a role in the early stages of ER Golgi protein trafficking. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.