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ELK Biotechnology AR (Acetyl Lys632) rabbit pAb
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ELK Biotechnology AR (Acetyl Lys632) rabbit pAb

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인간 AR(Androgen Receptor) Acetyl Lys632 특이 rabbit polyclonal antibody. WB와 ELISA에 적합하며, 고순도 IgG로 105kD 밴드 검출. 핵 및 세포질에서 발현되는 AR 연구에 활용 가능.

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pk
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ELK Biotechnology ES20055-100UL AR (Acetyl Lys632) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES20055-50UL AR (Acetyl Lys632) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology AR (Acetyl Lys632) rabbit pAb

제품명

AR (Acetyl Lys632) rabbit pAb

기본 정보

항목 내용
Alternative Names Androgen receptor (Dihydrotestosterone receptor; Nuclear receptor subfamily 3 group C member 4)
Applications WB; ELISA
Recommended Dilutions WB 1:1000–2000, ELISA 1:5000–20000
Immunogen Synthesized peptide derived from human AR (Acetyl Lys632)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 105 kD
GeneID (Human) 367
Human Swiss-Prot No P10275
Cellular Localization Nucleus, Cytoplasm. Detected at the promoter of target genes (PubMed:25091737). Predominantly cytoplasmic in unligated form but translocates to the nucleus upon ligand-binding. Can also translocate to the nucleus in unligated form in the presence of RACK1.
Species Reactivity Human; Mouse

Background

Defects in AR are associated with several diseases:

  • Androgen Insensitivity Syndrome (AIS): X-linked recessive pseudohermaphroditism due to end-organ resistance to androgen.
  • Partial Androgen Insensitivity Syndrome (PAIS): Also known as Reifenstein syndrome, characterized by hypospadias, hypogonadism, gynecomastia, and genital ambiguity.
  • Spinal and Bulbar Muscular Atrophy (SMAX1, Kennedy disease): X-linked recessive neuromuscular disorder caused by trinucleotide CAG repeat expansion.
  • Metastatic Prostate Cancer: Mutated AR stimulates prostate growth and metastasis despite androgen ablation.

Domain Structure

Composed of three domains:

  1. N-terminal modulating domain
  2. DNA-binding domain
  3. C-terminal steroid-binding domain

Agonist binding activates AR transcription factor activity through dimerization and DNA binding. Transcription is modulated by coactivator and corepressor proteins.

Function

Steroid hormone receptors are ligand-activated transcription factors regulating gene expression and cellular proliferation. Transcription activation is down-regulated by NR0B2 and activated by HIPK3.

Miscellaneous

  • Hormone binding increases receptor affinity for nuclear components.
  • Tyrosine phosphorylation level may predict response to hormone-ablation therapy.
  • Transcriptional activity enhanced by RANBP9 binding.

Polymorphisms

  • Poly-Gln region: Highly polymorphic (17–26 Gln); smaller size may be associated with prostate cancer.
  • Poly-Gly region: Polymorphic (24–31 Gly); shorter regions (≤23) may be associated with androgenetic alopecia.

Post-translational Modifications (PTM)

  • Phosphorylated in prostate cancer cells via c-Src kinase (CSK) at Tyr-534.
  • Sumoylated on Lys-386 (major) and Lys-520.

Similarity

Belongs to the nuclear hormone receptor family, NR3 subfamily. Contains one nuclear receptor DNA-binding domain.

Subunit Interactions

Binds DNA as homodimer. Forms complexes with EFCAB6/DJBP, PARK7, HIPK3, NR0B2, and others. Interacts with coactivators (NCOA1–4, MAGEA11) via LXXLL and FXXLF motifs. The N-terminal poly-Gln region binds Ran, enhancing AR-mediated transactivation.

Tissue Specificity

Isoform 2 is mainly expressed in heart and skeletal muscle.

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