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Anti-TMEM200A antibody

Cat.#: 176647

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Special Price 241.9 USD

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Product Information

  • Product Name
    Anti-TMEM200A antibody
  • Documents
  • Description
    Mouse monoclonal antibody to TMEM200A
  • Tested applications
    WB, ICC, IHC-P
  • Species reactivity
    Human, Mouse
  • Alternative names
    TTMA antibody; TTMC antibody; KIAA1913 antibody
  • Isotype
    IgG1
  • Preparation
    This antigen of this antibody was recombinant protein within human transmembrane protein 200a 50-400 aa.
  • Clonality
    Monoclonal
  • 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℃. Avoid repeated freeze / thaw cycles.
  • Applications

    WB: 1:500

    ICC: 1:100

    IHC-P: 1:50

  • Validations

    Fig1: Western blot analysis of Transmembrane protein 200A on A549 (1) and HepG2 (2) using anti-Transmembrane protein 200A antibody at 1/500 dilution.

    Fig1: Western blot analysis of Transmembrane protein 200A on A549 (1) and HepG2 (2) using anti-Transmembrane protein 200A antibody at 1/500 dilution.

    Fig2: ICC staining Transmembrane protein 200A (red) in F9 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig2: ICC staining Transmembrane protein 200A (red) in F9 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig3: ICC staining Transmembrane protein 200A (green) in HepG2 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig3: ICC staining Transmembrane protein 200A (green) in HepG2 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig4: ICC staining Transmembrane protein 200A (red) in NCCIT cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

    Fig4: ICC staining Transmembrane protein 200A (red) in NCCIT cells. 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 pancreas tissue using anti-Transmembrane protein 200A antibody. Counter stained with hematoxylin.

    Fig5: Immunohistochemical analysis of paraffin-embedded human pancreas tissue using anti-Transmembrane protein 200A antibody. Counter stained with hematoxylin.

  • Background
  • References
    • Hui A B Y et al. Identification of a novel homozygous deletion region at 6q23.1 in medulloblastomas using high-resolution array comparative genomic hybridization analysis. Clin Cancer Res 11:4707-4716 (2005).
    • Carninci P et al. The transcriptional landscape of the mammalian genome. Science 309:1559-1563 (2005).

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