PNPO Mouse Monoclonal Antibody (HRP conjugated) [Clone ID: OTI3B3]

CAT#: TA503249BM

PNPO mouse monoclonal antibody, clone OTI3B3 (formerly 3B3), HRP conjugated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY PNPO (RC200133, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-PNPO. Positive lysates LY413282 (100ug) and LC413282 (20ug) can be purchased separately from OriGene.

• 

  Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-PNPO monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).

• 

  Anti-PNPO mouse monoclonal antibody (TA503249) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY PNPO (RC200133).

Specifications

Product Data

• Clone Name: OTI3B3
• Applications: IF, WB
• Recommended Dilution: WB 1:500~2000, IF 1:100
• Reactivities: Human, Monkey, Mouse, Rat, Dog
• Host: Mouse
• Isotype: IgG2a
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human PNPO(NP_060599) produced in HEK293T cell.
• Formulation: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: HRP
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 29.8 kDa
• Gene Name: pyridoxamine 5'-phosphate oxidase
• Database Link:
  NP_060599
  Entrez Gene 64533 RatEntrez Gene 103711 MouseEntrez Gene 480540 DogEntrez Gene 694949 MonkeyEntrez Gene 55163 Human
  UniProt ID Q9NVS9
• Background: The enzyme encoded by this gene catalyzes the terminal, rate-limiting step in the synthesis of pyridoxal 5'-phosphate, also known as vitamin B6. Vitamin B6 is a required co-factor for enzymes involved in both homocysteine metabolism and synthesis of neurotransmitters such as catecholamine. Mutations in this gene result in pyridoxamine 5'-phosphate oxidase (PNPO) deficiency, a form of neonatal epileptic encephalopathy. [provided by RefSeq, Oct
• Synonyms: HEL-S-302; PDXPO

Reference Data

• Protein Pathways: Metabolic pathways, Vitamin B6 metabolism