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Anti-CD68 antibody

Cat.#: 175167

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Special Price 241.9 USD

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Product Information

  • Product Name
    Anti-CD68 antibody
  • Documents
  • Description
    Rabbit polyclonal antibody to CD68
  • Tested applications
    WB, FC
  • Species reactivity
    Human
  • Alternative names
    GP110 antibody; LAMP4 antibody; SCARD1 antibody
  • Isotype
    IgG
  • Preparation
    This antigen of this antibody was synthetic peptide within c-terminal human cd68.
  • Clonality
    Polyclonal
  • Formulation
    Liquid, 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
  • Storage instructions
    Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
  • Applications

    WB:1:500-1:1,000

    FC:1:50-1:100

  • Validations

    Fig1:; Western blot analysis of CD68 on human spleen tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody ( 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.

    Fig1:; Western blot analysis of CD68 on human spleen tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody ( 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.

    Fig2:; Flow cytometric analysis of CD68 was done on SiHa cells. The cells were fixed, permeabilized and stained with the primary antibody ( 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

    Fig2:; Flow cytometric analysis of CD68 was done on SiHa cells. The cells were fixed, permeabilized and stained with the primary antibody ( 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

  • Background
    P34810
  • References
    • Chistiakov DA. et. al. CD68/macrosialin: not just a histochemical marker. Lab Invest. 2017 Jan;97(1):4-13.
    • Tochio H. et. al. CD68-Positive Cells in Hepatic Angiomyolipoma. Oncology. 2017;92 Suppl 1:35-39.

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