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- Tel: 858.663.9055
- Email: info@nsjbio.com
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Ornithine aminotransferase (OAT) is an enzyme which is encoded in human by the OAT gene located on chromosome 10. 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.
Optimal dilution of the Ornithine Aminotransferase antibody should be determined by the researcher.
An E. coli-derived human protein (amino acids A214-F439) was used as the immunogen for the Ornithine Aminotransferase antibody.
After reconstitution, the Ornithine Aminotransferase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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