PNPO Mouse Monoclonal Antibody [Clone ID: OTI1G9]
CAT#: CF503506
Carrier-free (BSA/glycerol-free) PNPO mouse monoclonal antibody, clone OTI1G9 (formerly 1G9)
Formulation: Standard
Other products for "PNPO"
Specifications
Product Data | |
Clone Name | OTI1G9 |
Applications | FC, IHC, WB |
Recommended Dilution | WB 1:4000, IHC 1:150, FLOW 1:100 |
Reactivities | Human, Mouse, Rat |
Host | Mouse |
Isotype | IgG2a |
Clonality | Monoclonal |
Immunogen | Full length human recombinant protein of human PNPO(NP_060599) produced in HEK293T cell. |
Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Unconjugated |
Storage | Store at -20°C as received. |
Stability | Stable for 12 months from date of receipt. |
Predicted Protein Size | 29.8 kDa |
Gene Name | Homo sapiens pyridoxamine 5'-phosphate oxidase (PNPO), mRNA. |
Database Link | |
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]. COMPLETENESS: complete on the 3' end. |
Synonyms | HEL-S-302; PDXPO |
Reference Data | |
Protein Pathways | Metabolic pathways, Vitamin B6 metabolism |
Documents
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