CCD50 Rabbit Polyclonal Antibody, 20ul Cell Transfection This gene belongs to the

This gene belongs to the motin family of angiostatin binding proteins characterized by conserved coiled-coil domains and C-terminal PDZ binding motifs

Defects in this gene are the cause of hemochromatosis type 2A

IMP1 and IMP2 (IMMP2L

This gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum

and LIN2-like (see CASK

CCD50 Rabbit Polyclonal Antibody, 20ul Cell Transfection This gene belongs to theThis gene encodes a soluble, cytoplasmic, tyrosine phosphorylated protein with multiple ubiquitin interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule based structures. This protein may also function as a negative regulator of NF kB signaling and as an