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

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

P311 is expressed at lower levels in hippocampus

kidney and intestine and similar to aldolase C levels in brain and other nervous tissue

With a 150ml capacity

a characteristic unique to this subfamily

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).