Anti-FPR1 antibody

Cat.#: 176714

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Product Information

  • Product Name
    Anti-FPR1 antibody
  • Documents
  • Description
    Rabbit polyclonal antibody to FPR1
  • Tested applications
    WB, ICC, IHC-P, FC
  • Species reactivity
    Human, Mouse
  • Alternative names
    FPR antibody; FMLP antibody
  • Isotype
    IgG
  • Preparation
    This antigen of this antibody was peptide
  • Clonality
    Polyclonal
  • Formulation
    Liquid, 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
  • Storage instructions
    Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
  • Applications

    WB: 1:500

    ICC: 1:50-1:200

    IHC-P: 1:50-1:100

    FC: 1:50-1:100

  • Validations

    Fig1: Western blot analysis of FPR1 on different cell lysate using anti-FPR1 antibody at 1/500 dilution.; Positive control:; Lane 1: NCCIT Lane 2: MEF; Lane 3: HES

    Fig1: Western blot analysis of FPR1 on different cell lysate using anti-FPR1 antibody at 1/500 dilution.; Positive control:; Lane 1: NCCIT Lane 2: MEF; Lane 3: HES

    Fig2: ICC staining FPR1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig2: ICC staining FPR1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig3: ICC staining FPR1 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig3: ICC staining FPR1 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig4: ICC staining FPR1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig4: ICC staining FPR1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig5: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-FPR1 antibody. Counter stained with hematoxylin.

    Fig5: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-FPR1 antibody. Counter stained with hematoxylin.

    Fig6: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-FPR1 antibody. Counter stained with hematoxylin.

    Fig6: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-FPR1 antibody. Counter stained with hematoxylin.

    Fig7: Flow cytometric analysis of MCF-7 cells with FPR1 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black).

    Fig7: Flow cytometric analysis of MCF-7 cells with FPR1 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black).

  • Background
  • References

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"