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ELK Biotechnology AR rabbit pAb
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ELK Biotechnology AR rabbit pAb

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AR rabbit pAb는 인간, 마우스, 랫트에서 AR 단백질을 검출하기 위한 폴리클로날 항체로, IF, WB, IHC, ELISA에 적합합니다. 내부 유래 합성 펩타이드를 면역원으로 사용하며, 99kDa 밴드를 검출합니다. -20°C에서 1년 보관 가능합니다.

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pk
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ELK Biotechnology ES4268-100UL AR rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES4268-50UL AR rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology AR rabbit pAb

제품명

AR rabbit pAb

주요 정보

항목 내용
Alternative Names AR; DHTR; NR3C4; Androgen receptor; Dihydrotestosterone receptor; Nuclear receptor subfamily 3 group C member 4
Applications IF; WB; IHC; ELISA
Recommended Dilutions IF: 1:50–200, WB: 1:500–2000, ELISA: 1:10000–20000, IHC: 1:50–300
Immunogen Synthesized peptide derived from the internal region of human AR
Host Species Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 99 kDa
Gene ID (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, Rat

Background

The androgen receptor gene is more than 90 kb long and codes for a protein that has three 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 stimulates transcription of androgen-responsive genes.

This gene contains two 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 identified.

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