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ACP2 Antikörper

ACP2 Reaktivität: Human WB, IF, IHC (p), EIA Wirt: Maus Monoclonal M1-4A12 unconjugated
Produktnummer ABIN781949
  • Target Alle ACP2 Antikörper anzeigen
    ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
    Reaktivität
    • 18
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    Human
    Wirt
    • 16
    • 2
    Maus
    Klonalität
    • 16
    • 2
    Monoklonal
    Konjugat
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser ACP2 Antikörper ist unkonjugiert
    Applikation
    • 11
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    Spezifität
    This antibody reacts to ACP2 / Acid Phosphatase 2.
    Aufreinigung
    Affinity chromatography on Protein A
    Immunogen
    ACP2 antibody was raised against recombinant protein
    Klon
    M1-4A12
    Isotyp
    IgG2b
    Top Product
    Discover our top product ACP2 Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    0,41 mg/mL
    Buffer
    PBS, pH 7.2
    Handhabung
    Avoid repeated freezing and thawing.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
    Andere Bezeichnung
    ACP2 / LAP (ACP2 Produkte)
    Synonyme
    ACP2 antikoerper, Acp-2 antikoerper, LAP antikoerper, acid phosphatase 2, lysosomal antikoerper, acid phosphatase 2, lysosomal S homeolog antikoerper, ACP2 antikoerper, acp2 antikoerper, Acp2 antikoerper, acp2.S antikoerper
    Hintergrund
    Lysosomal acid phosphatase is comprised of two subunits, alpha and beta, and is chemically and genetically distinct from red cell acid phosphatase. Lysosomal acid phosphatase 2 is a member of a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Acid phosphatase deficiency is caused by mutations in the ACP2 (beta subunit) and ACP3 (alpha subunit) genes.Synonyms: Lysosomal acid phosphatase
    Gen-ID
    53
    NCBI Accession
    NP_001601
    UniProt
    P11117
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