ACADL Antikörper (N-Term)

Produktnummer ABIN2778158

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ACADL in WB. Er zeigt eine Reaktivität gegenüber Human, Maus, Ratte, Pferd, Schwein, Kaninchen, Rind (Kuh) und Hund.

Kurzübersicht für ACADL Antikörper (N-Term) (ABIN2778158)

Target: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Reaktivität: Human, Maus, Ratte, Pferd, Schwein, Kaninchen, Rind (Kuh), Hund

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ACADL Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-ACADL Antikörper

Bindungsspezifität: N-Term

Sequenz: MAARLLRGSL RVLGGHRAPR QLPAARCSHS GGEERLETPS AKKLTDIGIR

Homologie: Cow: 93%, Dog: 86%, Horse: 100%, Human: 100%, Mouse: 92%, Pig: 93%, Rabbit: 85%, Rat: 92%

Produktmerkmale: This is a rabbit polyclonal antibody against ACADL. It was validated on Western Blot using a cell lysate as a positive control.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N terminal region of human ACADL

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 430 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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 freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu ACADL

Target: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Andere Bezeichnung: ACADL

Hintergrund: ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in ACADL gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
Alias Symbols: ACAD4, LCAD
Protein Interaction Partner: Htt, UBC,
Protein Size: 430

Molekulargewicht: 44 kDa

Gen-ID: 33

NCBI Accession: NM_001608, NP_001599

UniProt: P28330

Pathways: Monocarboxylic Acid Catabolic Process