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WB analysis of LNCaP (A), UV-treated MCF7 (B), mouse spleen (C), rat spleen (D) whole cell lysates using GTX55077 Androgen Receptor (phospho Tyr363) antibody.
WB analysis of LNCaP (A), UV-treated MCF7 (B), mouse spleen (C), rat spleen (D) whole cell lysates using GTX55077 Androgen Receptor (phospho Tyr363) antibody.
WB analysis of LNCaP (A), UV-treated MCF7 (B), mouse spleen (C), rat spleen (D) whole cell lysates using GTX55077 Androgen Receptor (phospho Tyr363) antibody.

Androgen Receptor (phospho Tyr363) antibody

GTX55077
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetAR
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Overview

  • Supplier
    GeneTex
  • Product Name
    Androgen Receptor (phospho Tyr363) antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID367
  • Target name
    AR
  • Target description
    androgen receptor
  • Target synonyms
    AIS; androgen receptor; AR8; DHTR; dihydrotestosterone receptor; HUMARA; HYSP1; KD; NR3C4; nuclear receptor subfamily 3 group C member 4; SBMA; SMAX1; TFM
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP10275
  • Protein Name
    Androgen receptor
  • Scientific Description
    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 (SBMA, also known as Kennedys disease). Mutations in this gene are also associated with complete androgen insensitivity (CAIS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203