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Leadgene Leadgene
Anti-IL-8 Antibody [Clone 58-1]
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Catalog Number

LDG0030YA

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  • Overview

    Description

    The CXC chemokine is a group of secreted proteins, attracts neutrophils and lymphocytes. Interleukin-8 (IL-8, or CXCL8), a member of the CXC chemokines, is a proinflammatory cytokine produced by macrophages and other cell types like endothelial cells, epithelial cells and airways smooth muscle cells. This cytokine mainly attracts and activates neutrophils to the site of inflammation and also plays an important role in cell proliferation, tissue remodeling and angiogenesis.

    Product Note

    Recommended dilution factor:
    ELISA: 1:5000-20000
    WB: 1:1000-5000
    IFA: 1:500-1000
    FACS: Assay dependent

    Note: Working dilution for specific application should be determined by the investigator to obtain the best conditions.

  • Specifications
    • Host

      Mouse

      Clonality

      Monoclonal

    • Isotype

      IgG1

      Clone Name

      clone 58-1

    • Immunogen

      Interleukin 8

      Reactivity

      Human

    • Application

      ELISA, WB, IFA, FACS

      Conjugation

      Unconjugated

    • Concentration

      1 mg/mL

      Storage Buffer

      Phosphate Buffered Saline containing 0.03% ProClin 300, pH 7.4.

    • Specificity

      Interleukin 8

      Form

      Liquid

  • Instruction
    • Shipping

      The product is shipped with polar packs. Upon receipt, store it immediately at -20°C or lower for long term storage.

      Stability & Storage

      This product is stable after storage at:

      • 2-8°C for 2 weeks under sterile conditions from date of receipt.
      • -20°C or -80°C for 12 months under sterile conditions from date of receipt.

      Avoid repeated freeze/thaw cycles.
      Suggestion: Divide antibody into several vials. Keep only vials for usage at 2-8°C.

  • Image
    Immunofluorescence analysis of Anti-IL-8 Antibody [Clone 58-1] HeLa cells were fixed in 4% PFA, permeabilized with PBS containing 0.1% Triton X-100. Cells were stained with mouse anti-IL-8 monoclonal antibody (1:200) followed by secondary antibodies (goat anti-Mouse IgG-iFluor 488, 1:400, green) and cell nuclei were stained with Hoechst 33342 (Blue).

    Immunofluorescence analysis of Anti-IL-8 Antibody [Clone 58-1]
    HeLa cells were fixed in 4% PFA, permeabilized with PBS containing 0.1%
    Triton X-100. Cells were stained with mouse anti-IL-8 monoclonal antibody
    (1:200) followed by secondary antibodies (goat anti-Mouse IgG-iFluor 488,
    1:400, green) and cell nuclei were stained with Hoechst 33342 (Blue).

    FACS analysis of Anti-IL-8 Antibody [Clone 58-1] Human peripheral blood mononuclear cells (PBMC) were stained with mouse anti-IL-8 monoclonal antibody at 2 μg/ml (red) and without antibody control (black).

    FACS analysis of Anti-IL-8 Antibody [Clone 58-1]
    Human peripheral blood mononuclear cells (PBMC) were stained with mouse
    anti-IL-8 monoclonal antibody at 2 μg/ml (red) and without antibody control
    (black).

    ELISA titration of Anti-IL-8 Antibody [Clone 58-1] Titration curve of anti-IL-8 antibody in ELISA. Red: IL-8; Black: BSA (negative control).

    ELISA titration of Anti-IL-8 Antibody [Clone 58-1]
    Titration curve of anti-IL-8 antibody in ELISA. Red: IL-8; Black: BSA (negative
    control).

    Western blotting analysis of Anti-IL-8 Antibody [Clone 58-1] Recombinant IL-8 protein (100 ng) was stained with mouse anti-IL-8 monoclonal antibody at 1:5000 dilution.

    Western blotting analysis of Anti-IL-8 Antibody [Clone 58-1]
    Recombinant IL-8 protein (100 ng) was stained with mouse anti-IL-8
    monoclonal antibody at 1:5000 dilution.

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  • Datasheet & Documents
    MSDS
    Manual
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