Rabbit Hypoxanthine Phosphoribosyltransferase 1 Polyclonal Antibody | anti-HPRT1 antibody

Hypoxanthine Phosphoribosyltransferase 1 (HPRT1, HPRT, HGPRT) (APC)

Cat. Num. AAA6421866

• Gene Names: HPRT1; HPRT; HGPRT
• Reactivity: Human, Mouse, Rat
• Applications: Immunohistochemistry, Western Blot
• Purity: Purified by affinity chromatography.
• Synonyms: Hypoxanthine Phosphoribosyltransferase 1; Polyclonal Antibody; Hypoxanthine Phosphoribosyltransferase 1 (HPRT1; HPRT; HGPRT) (APC); anti-HPRT1 antibody

• Host: Rabbit
• Reactivity: Human, Mouse, Rat
• Clonality: Polyclonal
• Isotype: IgG
• Specificity: Recognizes HPRT1. Species Crossreactivity: human, mouse, rat
• Purity/Purification: Purified by affinity chromatography.
• Form/Format: Supplied as a liquid in PBS, pH 7.2. No preservative added. Labeled with Allophycocyanin (APC).
• Concentration: ~1mg/ml (varies by lot)

• Applicable Applications for anti-HPRT1 antibody: Immunohistochemistry (IHC), Western Blot (WB)
• Application Notes: IHC: 1:50-1:200; WB: 1:500-1:2000; Applications are based on unconjugated antibody.
• Immunogen: Recombinant protein corresponding to human HPRT1.
• Conjugate: APC
• Note: Preservative Free
• Preparation and Storage: Store product at 4 degree C in the dark. DO NOT FREEZE! Stable at 4 degree C for 12 months after receipt as an undiluted liquid. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Caution: APC conjugates are sensitive to light. For maximum recovery of product, centrifuge the original vial prior to removing the cap.

Western Blot (WB)

(Western blot analysis of extracts of various cell lines, using HPRT1 antibody.)

Product Categories/Family for anti-HPRT1 antibody

Antibodies; Disease Markers

NCBI and Uniprot Product Information

• NCBI GI #: 4504483
• NCBI GeneID: 3251
• NCBI Accession #: NP_000185.1
• NCBI GenBank Nucleotide #: NM_000194.2
• UniProt Accession #: P00492; A6NHF0; B2R8M9
• Molecular Weight: 24,579 Da
• NCBI Official Full Name: hypoxanthine-guanine phosphoribosyltransferase
• NCBI Official Synonym Full Names: hypoxanthine phosphoribosyltransferase 1
• NCBI Official Symbol: HPRT1
• NCBI Official Synonym Symbols: HPRT; HGPRT
• NCBI Protein Information: hypoxanthine-guanine phosphoribosyltransferase; HGPRTase
• UniProt Protein Name: Hypoxanthine-guanine phosphoribosyltransferase
• Protein Family: Hypoxanthine-guanine phosphoribosyltransferase
• UniProt Gene Name: HPRT1
• UniProt Synonym Gene Names: HPRT; HGPRT; HGPRTase
• UniProt Entry Name: HPRT_HUMAN

NCBI Description

The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009]

Uniprot Description

HPRT1: Converts guanine to guanosine monophosphate, and hypoxanthine to inosine monophosphate. Transfers the 5- phosphoribosyl group from 5-phosphoribosylpyrophosphate onto the purine. Plays a central role in the generation of purine nucleotides through the purine salvage pathway. Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS). LNS is characterized by complete lack of enzymatic activity that results in hyperuricemia, choreoathetosis, mental retardation, and compulsive self-mutilation. Defects in HPRT1 are the cause of gout HPRT-related (GOUT-HPRT); also known as HPRT-related gout or Kelley-Seegmiller syndrome. Gout is characterized by partial enzyme activity and hyperuricemia. Belongs to the purine/pyrimidine phosphoribosyltransferase family.

Protein type: Xenobiotic Metabolism - drug metabolism - other enzymes; Nucleotide Metabolism - purine; EC 2.4.2.8; Transferase; Cell development/differentiation

Chromosomal Location of Human Ortholog: Xq26.1

Cellular Component: cytoplasm; cytosol

Molecular Function: protein binding; protein homodimerization activity; magnesium ion binding; nucleotide binding; hypoxanthine phosphoribosyltransferase activity

Biological Process: hypoxanthine metabolic process; IMP salvage; cytolysis; adenine salvage; locomotory behavior; dopamine metabolic process; purine salvage; protein homotetramerization; cerebral cortex neuron differentiation; IMP metabolic process; hypoxanthine salvage; central nervous system neuron development; grooming behavior; lymphocyte proliferation; striatum development; nucleobase, nucleoside and nucleotide metabolic process; GMP salvage; dendrite morphogenesis; response to amphetamine; purine nucleotide biosynthetic process; purine base metabolic process; GMP catabolic process; positive regulation of dopamine metabolic process; purine ribonucleoside salvage; guanine salvage

Disease: Kelley-seegmiller Syndrome; Lesch-nyhan Syndrome