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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total PRPS1.
This gene encodes an enzyme that catalyzes the phosphoribosylation of ribose 5-phosphate to 5-phosphoribosyl-1-pyrophosphate, which is necessary for purine metabolism and nucleotide biosynthesis. Defects in this gene are a cause of phosphoribosylpyrophosphate synthetase superactivity, Charcot-Marie-Tooth disease X-linked recessive type 5 and Arts Syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: deafness 2, perceptive, congenital; deafness, X-linked 2, perceptive, congenital; dJ1070B1.2 (phosphoribosyl pyrophosphate synthetase 1); phosphoribosyl pyrophosphate synthase I; phosphoribosyl pyrophosphate synthetase I; phosphoribosylpyrophosphate synthetase (PRPS1) precursor; PRS-I; ribose-phosphate diphosphokinase 1; unnamed protein product
Gene Aliases: 2310010D17Rik; ARTS; CMTX5; DFN2; DFNX1; PPRibP; Prps-1; PRS-I; PRSI
UniProt ID: (Human) P60891, (Rat) P60892, (Mouse) Q9D7G0
Entrez Gene ID: (Human) 5631, (Rat) 29562, (Mouse) 19139
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