OAT anticorps

N° du produit ABIN5962963

Détail du produit anti-OAT anticorps

Antigène: OAT (Ornithine Aminotransferase (OAT))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OAT est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant protein of human OAT

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur OAT

Antigène: OAT (Ornithine Aminotransferase (OAT))

Autre désignation: OAT (OAT Produits)

Synonymes: anticorps 151832_at, anticorps CG8782, anticorps Dmel\\CG8782, anticorps hoga, anticorps AI194874, anticorps rOAT, anticorps GACR, anticorps HOGA, anticorps OATASE, anticorps OKT, anticorps Ornithine aminotransferase precursor, anticorps ornithine aminotransferase, gene 1, anticorps ornithine aminotransferase, anticorps Oat, anticorps oat.1, anticorps OAT, anticorps Lbys_2951, anticorps Riean_0998, anticorps Ftrac_2019, anticorps Celal_2605, anticorps Deipr_1149, anticorps Celly_0230, anticorps Weevi_2065, anticorps Fluta_4071, anticorps Halhy_2848, anticorps Theth_0565, anticorps oat

Sujet:

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.

Poids moléculaire:

Observed_MW: 47kDa

Calculated_MW: 32kDa/48kDa

ID gène: 4942

UniProt: P04181