ACAT1 anticorps (AA 1-145)

N° du produit ABIN6136413

Détail du produit anti-ACAT1 anticorps

Antigène: ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

Épitope: AA 1-145

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACAT1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Séquence: MAVLAALLRS GARSRSPLLR RLVQEIRYVE RSYVSKPTLK EVVIVSATRT PIGSFLGSLS LLPATKLGSI AIQGAIEKAG IPKEEVKEAY MGNVLQGGEG QAPTRQAVLG AGLPISTPCT TINKVCASGM KAIMMASQSL MCGHQ

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-145 of human ACAT1 (NP_000010.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

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 ACAT1

Antigène: ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

Autre désignation: ACAT1 (ACAT1 Produits)

Synonymes: anticorps ACAT, anticorps MAT, anticorps T2, anticorps THIL, anticorps RATACAL, anticorps 6330585C21Rik, anticorps Acat, anticorps fd16h07, anticorps fd20g06, anticorps wu:fd16h07, anticorps wu:fd20g06, anticorps zgc:86832, anticorps acat1-a, anticorps acetyl-CoA acetyltransferase 1, anticorps acetyl-Coenzyme A acetyltransferase 1, anticorps acetyl-CoA acetyltransferase 1 L homeolog, anticorps ACAT1, anticorps Acat1, anticorps acat1, anticorps acat1.L

Sujet: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.,ACAT1,ACAT,MAT,T2,THIL,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,Lipid Metabolism,ACAT1

Poids moléculaire: 42 kDa

ID gène: 38

UniProt: P24752