Anti-Gap43 antibody

Cat.#: 175796

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Product Information

  • Product Name
    Anti-Gap43 antibody
  • Documents
  • Description
    Rabbit polyclonal antibody to Gap43
  • Tested applications
    WB, ICC, IHC-P, FC
  • Species reactivity
    Human, Mouse, Rat
  • Alternative names
    Ba antibody; B-50 antibody; GAP- antibody; Basp2 antibody; GAP-43 antibody
  • Isotype
    Rabbit 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: 1:1,000

    ICC: 1:200

    IHC-P: 1:200

    FC: 1:100-1:200

  • Validations

    Fig1: Western blot analysis of GAP43 on different cell lysates using anti-GAP43 antibody at 1/1000 dilution.; Positive control:; Lane 1: Rat brain; Lane 2: Mouse brain; Lane 3: Mouse heart; Lane 4: Human skeletal muscle; Lane 5: N2A; Lane 6: A172; Lane 7: Human heart

    Fig1: Western blot analysis of GAP43 on different cell lysates using anti-GAP43 antibody at 1/1000 dilution.; Positive control:; Lane 1: Rat brain; Lane 2: Mouse brain; Lane 3: Mouse heart; Lane 4: Human skeletal muscle; Lane 5: N2A; Lane 6: A172; Lane 7: Human heart

    Fig2: ICC staining GAP43 in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig2: ICC staining GAP43 in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig3: ICC staining GAP43 in NIH/3T3 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig3: ICC staining GAP43 in NIH/3T3 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig4: ICC staining GAP43 in SHG-44 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig4: ICC staining GAP43 in SHG-44 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig5: ICC staining GAP43 in A172 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig5: ICC staining GAP43 in A172 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig6: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-GAP43 antibody. Counter stained with hematoxylin.

    Fig6: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-GAP43 antibody. Counter stained with hematoxylin.

    Fig7: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-GAP43 antibody. Counter stained with hematoxylin.

    Fig7: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-GAP43 antibody. Counter stained with hematoxylin.

  • Background
  • References
    • N-CAM modulates tumour-cell adhesion to matrix by inducing FGF-receptor signalling. Cavallaro U., Niedermeyer J., Fuxa M., Christofori G. Nat. Cell Biol. 3:650-657(2001)
    • Acyl-protein thioesterase 2 catalyzes the deacylation of peripheral membrane-associated GAP-43. Tomatis V.M., Trenchi A., Gomez G.A., Daniotti J.L. PLoS ONE 5:E15045-E15045(2010)

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