OAT antibody
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- Target See all OAT Antibodies
- OAT (Ornithine Aminotransferase (OAT))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This OAT antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human OAT
- Isotype
- IgG
- Top Product
- Discover our top product OAT Primary Antibody
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- Application Notes
- WB 1:500 - 1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- OAT (Ornithine Aminotransferase (OAT))
- Alternative Name
- OAT (OAT Products)
- Synonyms
- 151832_at antibody, CG8782 antibody, Dmel\\CG8782 antibody, hoga antibody, AI194874 antibody, rOAT antibody, GACR antibody, HOGA antibody, OATASE antibody, OKT antibody, Ornithine aminotransferase precursor antibody, ornithine aminotransferase, gene 1 antibody, ornithine aminotransferase antibody, Oat antibody, oat.1 antibody, OAT antibody, Lbys_2951 antibody, Riean_0998 antibody, Ftrac_2019 antibody, Celal_2605 antibody, Deipr_1149 antibody, Celly_0230 antibody, Weevi_2065 antibody, Fluta_4071 antibody, Halhy_2848 antibody, Theth_0565 antibody, oat antibody
- Background
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Synonyms: GACR,Gyrate atrophy,HOGA,OAT,OATASE,OKT,Ornithine aminotransferase (gyrate atrophy),Ornithine aminotransferase mitochondrial,ornithine aminotransferase precursor,Ornithine aminotransferase, mitochondrial precursor,Ornithine delta aminotransferase,Ornithine oxo acid 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.
- Molecular Weight
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Observed_MW: 47kDa
Calculated_MW: 32kDa/48kDa
- Gene ID
- 4942
- UniProt
- P04181
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