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OAT Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-73219
  • Amount:

    100ul
  • Price:

    225$
  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • Immunogen:

    Synthesized peptide derived from OAT . at AA range: 100-180
  • Source:

    Polyclonal, Rabbit
  • Gene Name:

    OAT
  • Dilution:

    Western Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.
  • Background:

    ornithine aminotransferase(OAT) Homo sapiens 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],
  • Protein Name:

    Ornithine aminotransferase mitochondrial
  • Human Gene Id:

    4942
  • Human Swiss Prot No:

    P04181
  • Mouse Gene Id:

    18242
  • Mouse Swiss Prot No:

    P29758
  • Rat Gene Id:

    64313
  • Rat Swiss Prot No:

    P04182
  • Specificity:

    OAT Polyclonal Antibody detects endogenous levels of OAT protein.
  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • Concentration:

    1 mg/ml
  • Storage Stability:

    -20°C/1 year
  • Other Name:

    OAT; Ornithine aminotransferase; mitochondrial; Ornithine delta-aminotransferase; Ornithine--oxo-acid aminotransferase
  • MolecularWeight(Da):

    48535
  • Observed Band(KD):

    48
  • Function:

    catalytic activity:L-ornithine + a 2-oxo acid = L-glutamate 5-semialdehyde + an L-amino acid.,cofactor:Pyridoxal phosphate.,disease:Defects in OAT are the cause of hyperornithinemia with gyrate atrophy of choroid and retina (HOGA) [MIM:258870]. HOGA is a slowly progressive blinding autosomal recessive disorder.,pathway:Amino-acid biosynthesis; L-proline biosynthesis; L-glutamate 5-semialdehyde from L-ornithine: step 1/1.,similarity:Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family.,subunit:Homotetramer.,
  • Subcellular Location:

    mitochondrion,mitochondrial matrix,
  • Expression:

    Alzheimer cortex,Brain,Cerebral cortex,Kidney,Liver,Placenta,Subthalamic nucleus,Ut

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Catalog Number

  • Amount:100ul
  • Price:225$

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AbPromise
OAT Polyclonal Antibody | EnoGene Biotech Co. Ltd