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ACP2 antibody

ACP2 Reactivity: Human WB, IF, IHC (p), EIA Host: Mouse Monoclonal M1-4A12 unconjugated
Catalog No. ABIN781949
  • Target See all ACP2 Antibodies
    ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
    Reactivity
    • 18
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    Human
    Host
    • 16
    • 2
    Mouse
    Clonality
    • 16
    • 2
    Monoclonal
    Conjugate
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ACP2 antibody is un-conjugated
    Application
    • 11
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    Specificity
    This antibody reacts to ACP2 / Acid Phosphatase 2.
    Purification
    Affinity chromatography on Protein A
    Immunogen
    ACP2 antibody was raised against recombinant protein
    Clone
    M1-4A12
    Isotype
    IgG2b
    Top Product
    Discover our top product ACP2 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    0,41 mg/mL
    Buffer
    PBS, pH 7.2
    Handling Advice
    Avoid repeated freezing and thawing.
    Storage
    4 °C/-20 °C
    Storage Comment
    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))
    Alternative Name
    ACP2 / LAP (ACP2 Products)
    Synonyms
    ACP2 antibody, Acp-2 antibody, LAP antibody, acid phosphatase 2, lysosomal antibody, acid phosphatase 2, lysosomal S homeolog antibody, ACP2 antibody, acp2 antibody, Acp2 antibody, acp2.S antibody
    Background
    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
    Gene ID
    53
    NCBI Accession
    NP_001601
    UniProt
    P11117
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