TRPV6 Polyclonal Antibody, 50ul Nucleic Acid Amplification Mutations in this gene have

Mutations in this gene have been found in some patients with the CHARGE syndrome

Another member of the CHP subfamily

beta (TSHB)

This gene encodes a member of the proteasome B-type family| also known as the T1B family| that is a 20S core beta subunit

The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function

TRPV6 Polyclonal Antibody, 50ul Nucleic Acid Amplification Mutations in this gene haveThis 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).