ACAT1 anticorps (AA 201-300) (Cy7)

N° du produit ABIN708467

Détail du produit anti-ACAT1 anticorps (Cy7)

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

Épitope: AA 201-300

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACAT1 est conjugé à/à la Cy7

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

Homologie: Human,Mouse,Rat,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, 0.03 % 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 (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:

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