CCD50 Rabbit Polyclonal Antibody, 20ul Cell Transfection IMP1 and IMP2 (IMMP2L

IMP1 and IMP2 (IMMP2L

SLC25A12 encodes a calcium-binding mitochondrial carrier protein

xeno-free hydrogel system that mimics the functions of native collagen

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

Catalytic activity of this enzyme promotes its nuclear localization

CCD50 Rabbit Polyclonal Antibody, 20ul Cell Transfection IMP1 and IMP2 (IMMP2LThis 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