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HADH Antikörper (AA 57-314)

Dieses Anti-HADH-Antikörper ist ein Huhn Polyklonal-Antikörper zur Detektion von HADH in WB. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN2468091

Kurzübersicht für HADH Antikörper (AA 57-314) (ABIN2468091)

Target

Alle HADH Antikörper anzeigen
HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

Reaktivität

  • 40
  • 37
  • 22
  • 8
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Maus, Ratte

Wirt

  • 42
  • 14
  • 1
Huhn

Klonalität

  • 44
  • 13
Polyklonal

Konjugat

  • 28
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser HADH Antikörper ist unkonjugiert

Applikation

  • 42
  • 16
  • 15
  • 13
  • 13
  • 12
  • 9
  • 9
  • 8
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 15
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 57-314

    Aufreinigung

    Immunoaffinity Purified
  • Applikationshinweise

    Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial antibody can be used for the detection of Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial by Western Blot.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline. No preservatives added.

    Konservierungsmittel

    Without preservative

    Handhabung

    As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    HADHSC antibody can be stored at 4 °C for short term (weeks). Long term storage should be at -20 °C.
  • Target

    HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

    Andere Bezeichnung

    HADHSC

    Hintergrund

    FUNCTION: Plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. Exerts it highest activity toward 3-hydroxybutyryl-CoA.

    DISEASE: Defects in HADHSC are the cause of 3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HAD deficiency) [MIM:609609]. HAD deficiency is a metabolic disorder with various clinical presentations including hypoglycemia, hepatoencephalopathy, myopathy or cardiomyopathy, and in some cases sudden death.

    Molekulargewicht

    34.3 kDa (calculated)

    Gen-ID

    3033

    NCBI Accession

    NP_005318

    UniProt

    Q16836

    Pathways

    Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
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