CCD50 Rabbit Polyclonal Antibody, 50ul Cryogenic Vials a genetic disorder whose symptoms

a genetic disorder whose symptoms include obesity

The most abundant form of NF-kappa-B is NFKB1 complexed with the product of the gene

Two alternatively spliced transcript variants encoding distinct proteins have been described

BAIAP2L1 encodes a member of the IMD (IRSp53/MIM homology domain) family

CCD50 Rabbit Polyclonal Antibody, 50ul Cryogenic Vials a genetic disorder whose symptomsThis 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