Anti-AR antibody

Cat.#: 141791

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Product Information

  • Product Name
    Anti-AR antibody
  • Documents
  • Description
    Mouse Monoclonal to Human AR
  • Tested applications
    ICC/IF, IF
  • Species reactivity
    Human Androgen receptor/NR3C4
  • Alternative names
    KD antibody; AIS antibody; TFM antibody; DHTR antibody; SBMA antibody; HYSP1 antibody; NR3C4 antibody; SMAX1 antibody; HUMARA antibody; Tfm antibody; AW320017 antibody
  • Isotype
    Mouse IgG1
  • Preparation
    This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with a synthetic peptide corresponding to the center region of the Human Androgen receptor/NR3C4. The IgG fraction of the cell culture supernatant was purified by Protein A affinity chromatography.
  • Clonality
    Monoclonal
  • Formulation
    0.2 μm filtered solution in PBS
  • Storage instructions
    This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free.
    Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.
  • Applications

    ICC/IF: 10-50 μg/mL

  • Validations

    Human Androgen receptor/NR3C4 Immunofluorescence(IF) 15375

    Human Androgen receptor/NR3C4 Immunofluorescence(IF) 15375

  • Background
    The androgen receptor gene is more than 90 kb long and codes for a protein that has 3 major functional domains: the N-terminal domain, DNA-binding domain, and androgen-binding domain. The protein functions as a steroid-hormone activated transcription factor. Upon binding the hormone ligand, the receptor dissociates from accessory proteins, translocates into the nucleus, dimerizes, and then stimulates transcription of androgen responsive genes. This gene contains 2 polymorphic trinucleotide repeat segments that encode polyglutamine and polyglycine tracts in the N-terminal transactivation domain of its protein. Expansion of the polyglutamine tract from the normal 9-34 repeats to the pathogenic 38-62 repeats causes spinal bulbar muscular atrophy (Kennedy disease). Mutations in this gene are also associated with complete androgen insensitivity (CAIS). Two alternatively spliced variants encoding distinct isoforms have been described.

    Immune Checkpoint   Immunotherapy   Cancer Immunotherapy   Targeted Therapy

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