| No | Size | Price | Availability | |
| ARP4942-61 | 50ul | 1500.00 | In Stock |  |
| ARP4942-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 4942 |
| Isotype: | IgG | Swiss Prot: | P04181 |
| purity: | Affinity purification |
| Background: |
| This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme is 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. [provided by RefSeq |
| Reactivity | Human, Mouse, Rat |
| Tested applications | WB |
| Clonality | Polyclonal Antibody |
| Calculated MW | 76 kDa |
| Recommended Dilutions |
WB 1:500-1:1000
|
| Immunogen | A synthetic peptide |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | DKFZp781A11155, GACR, gyrate atrophy, HOGA, OAT, OATASE, OKT, ornithine aminotransferase, Ornithine aminotransferase, hepatic form, Ornithine aminotransferase, mitochondrial, Ornithine aminotransferase, renal form, Ornithine--oxo-acid aminotransferase, or |
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