ARG56993
anti-OAT antibody [23A2]
anti-OAT antibody [23A2] for Flow cytometry,ICC/IF,Western blot and Human,Mouse
Overview
| Product Description | Mouse Monoclonal antibody [23A2] recognizes OAT |
|---|---|
| Tested Reactivity | Hu, Ms |
| Tested Application | FACS, ICC/IF, WB |
| Host | Mouse |
| Clonality | Monoclonal |
| Clone | 23A2 |
| Isotype | IgG1, kappa |
| Target Name | OAT |
| Antigen Species | Human |
| Immunogen | Recombinant fragment around aa. 33-439 of Human OAT. |
| Conjugation | Un-conjugated |
| Alternate Names | OATASE; OKT; Ornithine aminotransferase, mitochondrial; Ornithine--oxo-acid aminotransferase; GACR; HOGA; Ornithine delta-aminotransferase; EC 2.6.1.13 |
Application Instructions
| Application Suggestion |
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| Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Form | Liquid |
|---|---|
| Purification | Purification with Protein G. |
| Buffer | PBS (pH 7.4), 0.02% Sodium azide and 10% Glycerol. |
| Preservative | 0.02% Sodium azide |
| Stabilizer | 10% Glycerol |
| Concentration | 1 mg/ml |
| Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
| Database Links |
Swiss-port # P04181 Human Ornithine aminotransferase, mitochondrial Swiss-port # P29758 Mouse Ornithine aminotransferase, mitochondrial |
|---|---|
| Gene Symbol | OAT |
| Gene Full Name | ornithine aminotransferase |
| Background | This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome. [provided by RefSeq, Jan 2010] |
| Calculated MW | 49 kDa |
