TRPV6 Polyclonal Antibody, 20ul Cryogenic Vials Mutations in NRL have been

Mutations in NRL have been associated with retinitis pigmentosa and retinal degenerative diseases

SLC16A2 is expressed in many tissues and likely plays an important role in the development of the central nervous system

The insulin-like growth factor I receptor plays a critical role in transformation events

Alternative splicing results in multiple transcript variants

facilitating protein folding and assembly

TRPV6 Polyclonal Antibody, 20ul Cryogenic Vials Mutations in NRL have beenThis gene encodes a member of a family of multipass membrane proteins that functions as calcium channels. The encoded protein contains N terminal ankyrin repeats, which are required for channel assembly and regulation. Translation initiation for this protein occurs at a non AUG start codon that is decoded as methionine. This gene is situated next to a closely related gene for transient receptor potential cation channel subfamily V member 5 (TRPV5).