FA18A Rabbit Polyclonal Antibody, 50ul Shaker&Mixing memory B cell development

memory B cell development

Among its related pathways are Transport to the Golgi and subsequent modification and Surfactant metabolism

Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy| in particular limb-girdle muscular dystrophy| type 2C (LGMD2C)

The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha

EMR4P may represent a transcribed pseudogene

FA18A Rabbit Polyclonal Antibody, 50ul Shaker&Mixing memory B cell developmentThis gene encodes a membrane protein associated with the Golgi apparatus which plays a crucial role in intracellular vesicular transport. The encoded protein is likely associated with the late (trans) Golgi compartments which are involved in the delivery of secretory and membrane proteins to the endosome lysosome or the plasma membrane. Alternative splicing results in multiple transcript variants.