goat polyclonal IgG, 200 µg/ml; also available as rabbit IgG 200 µg/ml, sc-17087-R
epitope corresponding to phosphorylated Tyr 390 of AchRβ1 of human origin
recommended for detection of Tyr 390 phosphorylated AchRβ1 of mouse, rat and human origin by WB and IF; also reactive with additional species, including equine, canine, bovine and porcine
AchRβ1 Background Information Members of the ligand-gated ion channel receptor family are characterized by their fast transmitting response to neurotransmitters. Two important members of this family are the nicotinic acetylcholine and glutamate receptors, both of which are composed of five homologous subunits forming a transmembrane aqueous pore. These transmembrane receptors change conformation in response to their cognate neurotransmitter. Nicotinic acetylcholine receptors (AChRs) are found at the postsynaptic membrane of the neuromuscular junction and bind acetylcholine molecules, allowing ions to move through the pore. Glutamate receptors are found in the postsynaptic membrane of cells in the central nervous system. The activity that is generated at the synapse by the binding of acetylcholine is terminated by acetylcholinesterase, an enzyme that rapidly hydrolyzes acetylcholine. AChR∫1, also known as CHRNB, CMS1D, CMS2A, SCCMS or CHRNB1, is a 501 amino acid protein that belongs to the ligand-gated ionic channel family. Defects in the gene encoding AChR∫1 may be the cause of congenital myasthenic syndrome slow-channel type (SCCMS), which is characterized by muscle weakness affecting the axial and limb muscles, the ocular muscles and the facial and bulbar musculature.
p-AchRβ1 (Tyr 390) Product Citations
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