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ALDOA Antikörper (AA 2-364)

This anti-ALDOA antibody (ABIN7153211) is a Rabbit Polyclonal antibody detecting ALDOA in WB, ELISA, IHC. Suitable for Human.
Produktnummer ABIN7153211

Kurzübersicht für ALDOA Antikörper (AA 2-364) (ABIN7153211)

Target

Alle ALDOA Antikörper anzeigen
ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

Reaktivität

  • 86
  • 33
  • 31
  • 17
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 64
  • 16
  • 12
  • 2
Kaninchen

Klonalität

  • 74
  • 19
Polyklonal

Konjugat

  • 65
  • 7
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser ALDOA Antikörper ist unkonjugiert

Applikation

  • 75
  • 43
  • 31
  • 23
  • 22
  • 15
  • 10
  • 8
  • 7
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Bindungsspezifität

    • 11
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2-364

    Kreuzreaktivität

    Human, Ratte

    Aufreinigung

    >95%, Protein G purified

    Immunogen

    Recombinant Human Fructose-bisphosphate aldolase A protein (2-364AA)

    Isotyp

    IgG
  • Applikationshinweise

    Recommended dilution: WB:1:500-1:5000, IHC:1:20-1:200,

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

    Konservierungsmittel

    ProClin

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

    Andere Bezeichnung

    ALDOA

    Hintergrund

    Background: Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein .Defects in ALDOA are the cause of glycogen storage disease type 12 (GSD12) [MIM:611881], also known as red cell aldolase deficiency. A metabolic disorder associated with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.Belongs to the class I fructose-bisphosphate aldolase family.

    Aliases: ALDA antibody, Aldo1 antibody, ALDOA antibody, ALDOA_HUMAN antibody, Aldolase 1 antibody, Aldolase A antibody, Aldolase A fructose bisphosphatase antibody, Aldolase A fructose bisphosphate antibody, Aldolase, fructose-bisphosphate A antibody, Epididymis secretory sperm binding protein Li 87p antibody, FRUCTOALDOLASE A antibody, Fructose 1 6 bisphosphate triosephosphate lyase antibody, Fructose bisphosphate aldolase A antibody, Fructose bisphosphate aldolase antibody, FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE A antibody, Fructose-bisphosphate aldolase A antibody, Fructose-bisphosphate aldolase A Muscle-type antibody, GSD12 antibody, HEL S 87p antibody, Lung cancer antigen NY LU 1 antibody, Lung cancer antigen NY-LU-1 antibody, MGC10942 antibody, MGC17716 antibody, MGC17767 antibody, Muscle type aldolase antibody, Muscle-type aldolase antibody, RNALDOG5 antibody

    UniProt

    P04075

    Pathways

    Ribonucleoside Biosynthetic Process
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