DMA Polyclonal Antibody, 20ul Immune Repertoire Sequencing this gene is disrupted in

this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion

PTPs catalyze the hydrolysis of the phosphate monoesters specifically on tyrosine residues

Alternatively spliced transcript variants encoding distinct isoforms have been observed

and thrombospondin N-terminal-like domains

a form of hereditary spastic paraplegia (HSP)

DMA Polyclonal Antibody, 20ul Immune Repertoire Sequencing this gene is disrupted inHLA DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes,