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AGA Antikörper (Middle Region)

AGA Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN926652
  • Target Alle AGA Antikörper anzeigen
    AGA (Aspartylglucosaminidase (AGA))
    Bindungsspezifität
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reaktivität
    • 20
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Human
    Wirt
    • 20
    • 1
    Kaninchen
    Klonalität
    • 21
    Polyklonal
    Konjugat
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser AGA Antikörper ist unkonjugiert
    Applikation
    • 11
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Aufreinigung
    Purified
    Immunogen
    AGA antibody was raised in rabbit using the middle region of AGA as the immunogen
    Top Product
    Discover our top product AGA Primärantikörper
  • Applikationshinweise
    Optimal conditions should be determined by the investigator.
    Kommentare

    AGA Blocking Peptide, catalog no. 33R-10401, is also available for use as a blocking control in assays to test for specificity of this AGA antibody

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Konzentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target
    AGA (Aspartylglucosaminidase (AGA))
    Andere Bezeichnung
    AGA (AGA Produkte)
    Synonyme
    AGU antikoerper, ASRG antikoerper, GA antikoerper, AW060726 antikoerper, aspartylglucosaminidase antikoerper, AGA antikoerper, Aga antikoerper
    Hintergrund
    Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. Synonyms: Polyclonal AGA antibody, Anti-AGA antibody, aspartylglucosaminidase antibody, AGU antibody, ASRG antibody, GA antibody.
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