OAT antibody (AA 100-180)

Catalog No. ABIN7862455

The Rabbit Polyclonal anti-OAT antibody (ABIN7862455) specifically detects OAT in WB and ELISA. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for OAT antibody (AA 100-180) (ABIN7862455)

Target: OAT (Ornithine Aminotransferase (OAT))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This OAT antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-OAT Antibody

Binding Specificity: AA 100-180

Purpose: Rabbit Anti-OAT Polyclonal Antibody

Specificity: OAT Polyclonal Antibody detects endogenous levels of OAT protein.

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

Immunogen: Synthesized peptide derived from the Internal region of human OAT at AA range: 100-180

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,ELISA 1:5000,Not yet tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for OAT

Target: OAT (Ornithine Aminotransferase (OAT))

Alternative Name: OAT

Background: OAT, Ornithine aminotransferase, mitochondrial, Ornithine delta-aminotransferase, Ornithine--oxo-acid aminotransferaseOAT 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: 48kD

Gene ID: 4942

UniProt: P04181