PHEX Antibody – Rabbit Polyclonal

The amyloid beta-peptide (Ab) of 39-43aa (Ab40, Ab42, Ab43) is constitutively produced in brain upon proteolysis of the b-amyloid precursor protein (APP). In the young and healthy humans, Ab is rapidly catabolized before it can be deposited in the brain. However, upon aging or the onset of familial Alzheimer's Disease, alterations in either synthesis or degradation/clearance of Ab may contribute to amyloid depositions in the brain. Ab is susceptible to a number of in vivo and in vitro proteases like cathepsin-D and M-13 metalloproteases. The M-13 family includes several members of zinc-dependent proteases like damage-induced neuronal endopeptidase (DINE), product of phosphate regulating gene with homologies to endopeptidases on the X chromosome (PHEX), neutral endopeptidase 24.11 or neprilysin (NEP) and neprilysin-like proteases (NEPLs). NEPLs (alpha, beta, gamma) arise from the alternative splicing of a single NELPS gene and show ~54% sequence homology. M13 members are generally type II transmembrane proteins consisting of a single polypeptide chain with Zinc binding HEXXH motif, a short cytoplasmic tail, a transmembrane segment and an extra-cytoplasmic domain containing the enzyme active site. Phosphate regulating gene with homologies to endopeptidases on the X chromosome (PHEX) (formerly PEX) is a zinc-containing, type II integral membrane glycoprotein (~110kD; mouse/rat/human: 749aa; chromosome xp22.2-p22.1) with structural resemblance to M13 NEP proteases. In contrast to NEP, PHEX has very narrow substrate specificity and hydrolyzes parathroid hormone related peptide (PTHrP107-139). Compared to NEP, PHEX can proteolyze Ab40 (but not Ab42), at a very low rate and to a very poor extent and therefore is not a major in vivo peptidase for Ab. However, it might degrade Ab in Alzheimer patients where Ab is accumulated in excess and an Ab-degradative pathway, alternative to NEP, exists. PHEX is expressed lymphocytes and fetal brain but not in adult brain, placenta, skeletal muscle, pancreas, heart, liver and lung. Defects in PHEX are a cause of X-linked hypophosphatemic rickets (HYP). PHEX is implicated in bone and dentin mineralization and renal phosphate reabsorption.

Small volumes of anti-PHEX antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS611265 is an antibody targeting PHEX. Also known as PHEX (PEX, Phosphate-regulating Gene with Homologies to Endopeptidases on the X Chromosome). Reactive in Rat. Host: Rabbit.