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  • Anti-BPI antibody
  • Anti-BPI antibody

Anti-BPI antibody

Cat.#: 176527

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Special Price 241.9 USD

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Product Information

  • Product Name
    Anti-BPI antibody
  • Documents
  • Description
    Rabbit monoclonal antibody to BPI
  • Tested applications
    WB, FC
  • Species reactivity
    Human, Zebrafish
  • Alternative names
    rBPI antibody; BPIFD1 antibody
  • Isotype
    IgG
  • Preparation
    This antigen of this antibody was synthetic peptide within human bpi aa 120-170.
  • Clonality
    Monoclonal
  • Formulation
    Liquid, 1*TBS (pH7.4), 0.05% 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: 1:1,000-1:2,000

    FC: 1:50-1:100

  • Validations

    Fig1:; Western blot analysis of BPI on THP-1 cell 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 1:40,000 dilution was used for 1 hour at room temperature.

    Fig1:; Western blot analysis of BPI on THP-1 cell 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 1:40,000 dilution was used for 1 hour at room temperature.

    Fig2:; Flow cytometric analysis of BPI was done on Jurkat 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 BPI was done on Jurkat 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
  • References
    • Hu, N. et al. 2014. Differential expression of granulopoiesis related genes in neutrophil subsets distinguished by membrane expression of CD177. PloS one. 9: e99671.
    • Ota T., et al. 2004. Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat. Genet. 36:40-45.

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