OAT antibody

Catalog No. ABIN2855721

This anti-OAT antibody is a Rabbit Polyclonal antibody detecting OAT in WB, IF, ICC and IHC (p). Suitable for Human.

Quick Overview for OAT antibody (ABIN2855721)

Target: OAT (Ornithine Aminotransferase (OAT))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This OAT antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-OAT Antibody

Cross-Reactivity: Human, Mouse

Characteristics: Rabbit Polyclonal antibody to OAT (ornithine aminotransferase)
OAT antibody [N1C3]

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human OAT. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:1000-1:10000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: Mouse brain , K562 , THP-1 , OAT-transfected 293T

Validation: Overexpression

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.28 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for OAT

Target: OAT (Ornithine Aminotransferase (OAT))

Alternative Name: ornithine aminotransferase

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.

Cellular Localization: Mitochondrion matrix

Molecular Weight: 49 kDa

Gene ID: 4942

UniProt: P04181