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S100A8 antibody (Biotin)

S100A8 Reactivity: Human WB, IHC (p), IHC (fro), EIA Host: Mouse Monoclonal 8-5C2 Biotin
Catalog No. ABIN111891
  • Target See all S100A8 Antibodies
    S100A8 (S100 Calcium Binding Protein A8 (S100A8))
    Reactivity
    • 83
    • 51
    • 33
    • 14
    • 10
    • 7
    • 6
    • 6
    • 6
    • 6
    • 4
    • 4
    • 4
    Human
    Host
    • 80
    • 37
    • 3
    • 3
    • 1
    • 1
    Mouse
    Clonality
    • 86
    • 39
    Monoclonal
    Conjugate
    • 64
    • 20
    • 16
    • 7
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This S100A8 antibody is conjugated to Biotin
    Application
    • 73
    • 46
    • 43
    • 31
    • 16
    • 15
    • 14
    • 14
    • 13
    • 12
    • 7
    • 6
    • 5
    • 5
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Enzyme Immunoassay (EIA)
    Specificity
    This Monoclonal antibody 8-5C2 detects a very distinct epitope in the central part of the molecule, in between the two Ca2+-binding domains (different from the S 13.67 epitope). This antibody identifies the Ca2+-binding light subunit of the inflammatory L-1 protein complex, also called S100A8 or Calgranulin A. It is useful for the identification of the 8 kDa subunit in various immunological techniques. Histological and serological data indicate that MRP8 is associated with chronic stages of inflammatory diseases. Antigen Distribution Isolated Cells: The antigen is found in granulocytes and monocytes but not in other blood cells. In cultured monocytes, maximum MRP8 is expressed after 3-4 days. Myeloid leukemia stain positive. Tissue Sections: In tissues MRP8 is found in a distinct subpopulation of inflammatory perivascular infiltrates of the myelo-monocytic lineage. Macrophages synthesise MRP8 increasingly during the late stages of inflammation. A low MRP8 (and high MRP-14) expression by macrophages was also reported in granulomatous diseases such as tuberculosis and sarcoidis. In non-granulomatous chronic inflammatory diseases such as chronic rheumatoid arthritis or chronic rejection after allograft transplantation, MRP8 and MRP14 positive cells consist of different subpopulations. The antibody reacts with Bovine spleen but does not react with Rat tissues. It shows a diffuse reaction with Swine spleen.
    Cross-Reactivity (Details)
    Species reactivity (tested):Human: MRP8 in stimulated monocytes and macrophages in late phase or chronic inflammation.
    Purification
    Protein A Chromatography
    Immunogen
    Cultured Human monocytes. Remarks: The antigen is MRP8, the epitope is suspected in the central portion of the peptide.
    Clone
    8-5C2
    Isotype
    IgG1
    Top Product
    Discover our top product S100A8 Primary Antibody
  • Application Notes
    ELISA. Flow Cytometry. Immunohistochemistry (IHC) on: Frozen Sections: 2 μg/mL (1/100). Paraffin Sections: 5-10 μg/mL (1/20-1/50). No pretreatment for antigen retrieval necessary,microwave treatment in 0.01M citrate pH 6.0 may enhance the reactivity. Suggested positive control: Human tonsil. Has been described to work Dot blots.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Restrictions
    For Research Use only
  • Reconstitution
    Restore with 0.5 mL distilled water (This stock solution contains 0.2 mg/mL IgG).
    Concentration
    0.2 mg/mL
    Buffer
    PBS, pH 7.2, 0.05 % (v/v) Kathon, 5 mg/mL BSA
    Preservative
    Thimerosal (Merthiolate)
    Precaution of Use
    This product contains thimerosal (merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Dilute only prior to immediate use
    Storage
    4 °C
    Storage Comment
    Store the antibody at 2-8 °C before opening. DO NOT FREEZE! This product is stable at 2-8 °C as an undiluted liquid. Freezing alkaline phosphatase conjugates will result in a substantial loss of enzymatic activity.
  • Wong, Zhou, Li, Tong, Zhao, Li, Yu, Koh, Beuerman: "Proteomic profiling of inflammatory signaling molecules in the tears of patients on chronic glaucoma medication." in: Investigative ophthalmology & visual science, Vol. 52, Issue 10, pp. 7385-91, (2011) (PubMed).

    Mortezai, Harder, Schnabel, Moors, Gauly, Schlüter, Wagener, Buck: "Tandem affinity depletion: a combination of affinity fractionation and immunoaffinity depletion allows the detection of low-abundance components in the complex proteomes of body fluids." in: Journal of proteome research, Vol. 9, Issue 12, pp. 6126-34, (2010) (PubMed).

    Soupene, Serikov, Kuypers: "Characterization of an acyl-coenzyme A binding protein predominantly expressed in human primitive progenitor cells." in: Journal of lipid research, Vol. 49, Issue 5, pp. 1103-12, (2008) (PubMed).

    Rosenberger, Thorey, Werner, Boukamp: "A novel regulator of telomerase. S100A8 mediates differentiation-dependent and calcium-induced inhibition of telomerase activity in the human epidermal keratinocyte line HaCaT." in: The Journal of biological chemistry, Vol. 282, Issue 9, pp. 6126-35, (2007) (PubMed).

    Zaba, Cardinale, Gilleaudeau, Sullivan-Whalen, Suárez-Fariñas, Suárez Fariñas, Fuentes-Duculan, Novitskaya, Khatcherian, Bluth, Lowes, Krueger: "Amelioration of epidermal hyperplasia by TNF inhibition is associated with reduced Th17 responses." in: The Journal of experimental medicine, Vol. 204, Issue 13, pp. 3183-94, (2007) (PubMed).

    Pedersen, Oster, Bundgaard, Höllsberg: "Induction of cell-cell fusion from without by human herpesvirus 6B." in: Journal of virology, Vol. 80, Issue 19, pp. 9916-20, (2006) (PubMed).

    Lukás, Dráber, Bucek, Dráberová, Viklický, Dolezel: "Expression of phosphorylated high molecular weight neurofilament protein (NF-H) and vimentin in human developing dorsal root ganglia and spinal cord." in: Histochemistry, Vol. 100, Issue 6, pp. 495-502, (1994) (PubMed).

    Bártek, Bártková, Vojt?sek, Stasková, Lukás, Rejthar, Kovarík, Midgley, Gannon, Lane: "Aberrant expression of the p53 oncoprotein is a common feature of a wide spectrum of human malignancies." in: Oncogene, Vol. 6, Issue 9, pp. 1699-703, (1991) (PubMed).

  • Target
    S100A8 (S100 Calcium Binding Protein A8 (S100A8))
    Alternative Name
    S100A8 / Calgranulin-A / MRP8 (S100A8 Products)
    Synonyms
    60B8AG antibody, CAGA antibody, CFAG antibody, CGLA antibody, CP-10 antibody, L1Ag antibody, MA387 antibody, MIF antibody, MRP8 antibody, NIF antibody, P8 antibody, Mrp8 antibody, S100A8 antibody, 60B8Ag antibody, AI323541 antibody, B8Ag antibody, CFAg antibody, Caga antibody, p8 antibody, MRP-8 antibody, S100 calcium binding protein A8 antibody, S100 calcium binding protein A8 (calgranulin A) antibody, S100A8 antibody, S100a8 antibody
    Background
    Synonyms: CAGA, CFAG, Calprotectin L1L subunit, Cystic fibrosis antigen, Leukocyte L1 complex light chain, MRP-8, Migration inhibitory factor-related protein 8, S100 calcium-binding protein A8, S100-A8, Urinary stone protein band A
    Gene ID
    9606
    UniProt
    P05109
    Pathways
    Transition Metal Ion Homeostasis, Positive Regulation of Endopeptidase Activity, S100 Proteins
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