ACAT1 anticorps (AA 201-300) (AbBy Fluor® 555)

N° du produit ABIN881025

Cet anticorps anti-ACAT1 Polyclonal Lapin conjugué à AbBy Fluor® 555 (ABIN881025) détecte spécifiquement ACAT1 dans IF (p) et IF (cc). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour ACAT1 anticorps (AA 201-300) (AbBy Fluor® 555) (ABIN881025)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACAT1 est conjugé à/à la AbBy Fluor® 555

Application: Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))

Détail du produit anti-ACAT1 anticorps (AbBy Fluor® 555)

Épitope: AA 201-300

Fonction: ACAT1 Polyclonal Antibody, AbBy Fluor-555 Conjugated

Réactivité croisée: Souris, Rat

Homologie: Human,Dog,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ACAT1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P)(1:50-200), IF(IHC-F)(1:50-200), IF(ICC)(1:50-200)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur ACAT1

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

Autre désignation: ACAT1

Sujet:

Synonyms: ACAT 1, ACAT, Acetoacetyl CoA thiolase, Acetyl CoA acetyltransferase, mitochondrial, Acetyl Coenzyme A acetyltransferase 1, MAT, RATACAL, T2, THIL, THIL_HUMAN, Acetyl-CoA acetyltransferase, mitochondrial, Acetoacetyl-CoA thiolase, T2.

Background: 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. [provided by RefSeq, Feb 2009].

ID gène: 38

UniProt: P24752