ACAT1 Antikörper (AA 34-427)

Produktnummer ABIN1449417

Produktdetails anti-ACAT1 Antikörper

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

Bindungsspezifität: AA 34-427

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser ACAT1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Aufreinigung: Protein-A affinity chromatography

Immunogen: Recombinant Human ACAT1 (34-427aa) purified from E. coli

Klon: AT15E5

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1.0 mg/mL

Buffer: Phosphate -Buffered Saline ( pH 7.4), 0.01 % Sodium Azide, 10 % Glycerol

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu ACAT1

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

Andere Bezeichnung: ACAT1 / MAT (ACAT1 Produkte)

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

Hintergrund: ACAT1 (acetyl-Coenzyme A acetyltransferase 1) is a 417 amino acid protein. ACAT1 is a mitochondrial enzyme involved in the formation and degradation of ketone bodies and is necessary for the proper metabolic processing of isoleucine. ACAT1 and ACAT2 catalyze the formation of acetoacetyl-CoA from two acetyl-CoA molecules. These enzymes are also capable of the reverse reaction. Defects in ACAT1 are a cause of 3-ketothiolase deficiency. 3-ketothiolase deficiency is an inborn error of isoleucine catabolism characterized by intermittent ketoacidotic attacks associated with unconsciousness. Some patients die during an attack or are mentally retarded.Synonyms: Acetoacetyl-CoA thiolase T2, Acetyl-CoA acetyltransferase mitochondrial

Gen-ID: 38

NCBI Accession: NP_000010

UniProt: P24752