ACAT1 Antikörper (AA 1-145)
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- Target Alle ACAT1 Antikörper anzeigen
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
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Bindungsspezifität
- AA 1-145
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser ACAT1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- Sequenz
- MAVLAALLRS GARSRSPLLR RLVQEIRYVE RSYVSKPTLK EVVIVSATRT PIGSFLGSLS LLPATKLGSI AIQGAIEKAG IPKEEVKEAY MGNVLQGGEG QAPTRQAVLG AGLPISTPCT TINKVCASGM KAIMMASQSL MCGHQ
- Kreuzreaktivität
- Human, Maus, Ratte
- Produktmerkmale
- Polyclonal Antibodies
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-145 of human ACAT1 (NP_000010.1).
- Isotyp
- IgG
- Top Product
- Discover our top product ACAT1 Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Andere Bezeichnung
- ACAT1 (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
- 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
- Molekulargewicht
- 42 kDa
- Gen-ID
- 38
- UniProt
- P24752
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