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Androgen receptor/NR3C4 Monoclonal Antibody (AN200154P)

Androgen receptor/NR3C4 Monoclonal Antibody - 1
  • Androgen receptor/NR3C4 Monoclonal Antibody - 1
  • Androgen receptor/NR3C4 Monoclonal Antibody - 2
All Size Price Qty
100μL $ 320.00
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For research use only.

Verified Samples Verified Samples in IF: HepG2, DU145
Dilution ICC/IF 1:20-1:100
Isotype IgG1
Host Mouse
Reactivity Human
Applications ICC/IF
Clonality Monoclonal
Immunogen A synthetic peptide corresponding to the center region of the Human Androgen receptor/NR3C4
Abbre AR
Synonyms HYSP,  NR3C,  SMAX,  AIS,  AR8,  DHTR,  HUMARA,  HYSP1,  KD,  NR3C4,  SBMA,  SMAX1,  TFM,  AR,  AIS,  AR8,  DHTR,  HUMARA,  HYSP1,  KD,  NR3C4,  SBMA,  SMAX1,  TFM,  AR,  Group C,  Member 4,  Nuclear Receptor Subfamily 3
Swissprot
Tissue Specificity Isoform 2 is mainly expressed in heart and skeletal muscle
Concentration 1 mg/mL
Buffer 0.2 μm filtered solution in PBS
Purification Method Protein A
Research Areas Signal Transduction,  Epigenetics and Nuclear Signaling,  Cancer,  Developmental Biology
Clone No. 1A9
Conjugation Unconjugated
Storage 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. Avoid repeated freeze-thaw cycles.
Shipping Ice bag
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.
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Unconjugated

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