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Thermo Fisher Scientific Androgen Receptor (ARv7 Splice Variant) Polyclonal Antibody
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Thermo Fisher Scientific Androgen Receptor (ARv7 Splice Variant) Polyclonal Antibody

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Androgen Receptor(ARv7) 스플라이스 변이체를 인식하는 토끼 폴리클로날 항체로, Western blot 및 IHC(P) 분석에 적합. 항원 친화 크로마토그래피로 정제되었으며, 인간 및 마우스 시료에 반응. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오전 09:31
Thermo Fisher Scientific PA5119517 Androgen Receptor (ARv7 Splice Variant) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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687,200원VAT 포함 755,920원

Thermo Fisher Scientific · Thermo Fisher Scientific Androgen Receptor (ARv7 Splice Variant) Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:3,000 -
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent -

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human Androgen Receptor (ARv7 Splice Variant).
Conjugate Unconjugated
Form Liquid
Concentration 1.83 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol
Contains 0.025% ProClin 300
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2913091

Product Specific Information

Store as concentrated solution. Centrifuge briefly prior to opening vial.
For short-term storage (1–2 weeks), store at 4°C.
For long-term storage, aliquot and store at -20°C or below.
Avoid multiple freeze-thaw cycles.


Target Information

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 then 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 (SBMA, also known as Kennedy’s 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]


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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