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