Overview
- Product nameAndrogen Receptor ELISA Kit
- Tests1 x 96 well plate
- Sample typeCell culture extracts, Tissue Extracts
- Assay typeSandwich
- Sensitivity> 600 ng/well
- Range600 ng/well - 10000 ng/well
- Assay time4h 00m
- Species reactivityReacts with: Dog, Human
- Product overview
Androgen Receptor (AR) belongs to the nuclear receptor (NR) superfamily of structurally related ligand-inducible transcription factors. NRs act in combination with other transcription factors to regulate the expression of gene networks involved in cell growth and development, apoptosis, homeostasis, inflammation, lipid metabolism, the reproductive cycle and other fundamental biological processes. AR expression plays an important role in the proliferation of human prostate cancer and also confers a better prognosis in breast cancer. Because of AR’s critical role in cell biology, it is important to measure the total amounts of AR contained in different cell types and tissues. Traditional methods for monitoring AR protein levels, such as Western blotting, EMSA, immunohistochemistry (IHC) and reporter gene assays, are time consuming and not suitable to high-throughput applications.
Abcam’s Androgen Receptor ELISA kit simplifies the measurement of AR contained in cell and tissue samples by using the “Sandwich ELISA” method for detecting a protein. This method uses two antibodies that each recognize a distinct epitope on the protein of interest. The kit provides an ELISA plate that is coated with the first antibody, called the Capture Antibody, which is used to capture the protein from the sample. The second antibody, called the Detecting Antibody, is used to detect the protein bound by the Capture Antibody. An HRP-conjugated Secondary Antibody is then used to quantitate the amount of bound Detecting Antibody. Subsequent incubation with developing solution provides an easily quantified colorimetric readout.
- Tested applicationsSandwich ELISA more details
Properties
- Storage instructionsPlease refer to protocols.
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Components 1 x 96 tests 96-well assay plate 1 unit AR detection antibody 1 x 26µl Developing solution 1 x 11ml Diluent Buffer 1 x 22ml HRP-conjugated antibody 1 x 6µl LNCaP nuclear extract 1 x 40µl Plate sealer 1 unit Stop Solution 1 x 11ml Wash Buffer 1 x 22ml -
Research Areas
Defects in AR are the cause of spinal and bulbar muscular atrophy X-linked type 1 (SMAX1) [MIM:313200]; also known as Kennedy disease. SMAX1 is an X-linked recessive form of spinal muscular atrophy. Spinal muscular atrophy refers to a group of neuromuscular disorders characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy. SMAX1 occurs only in men. Age at onset is usually in the third to fifth decade of life, but earlier involvement has been reported. It is characterized by slowly progressive limb and bulbar muscle weakness with fasciculations, muscle atrophy, and gynecomastia. The disorder is clinically similar to classic forms of autosomal spinal muscular atrophy. Note=Caused by trinucleotide CAG repeat expansion. In SMAX1 patients the number of Gln ranges from 38 to 62. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
Note=Defects in AR may play a role in metastatic prostate cancer. The mutated receptor stimulates prostate growth and metastases development despite of androgen ablation. This treatment can reduce primary and metastatic lesions probably by inducing apoptosis of tumor cells when they express the wild-type receptor.
Defects in AR are the cause of androgen insensitivity syndrome partial (PAIS) [MIM:312300]; also known as Reifenstein syndrome. PAIS is characterized by hypospadias, hypogonadism, gynecomastia, genital ambiguity, normal XY karyotype, and a pedigree pattern consistent with X-linked recessive inheritance. Some patients present azoospermia or severe oligospermia without other clinical manifestations.
Contains 1 nuclear receptor DNA-binding domain.
modificationsSumoylated on Lys-386 (major) and Lys-520. Ubiquitinated. Deubiquitinated by USP26. 'Lys-6' and 'Lys-27'-linked polyubiquitination by RNF6 modulates AR transcriptional activity and specificity.
Phosphorylated in prostate cancer cells in response to several growth factors including EGF. Phosphorylation is induced by c-Src kinase (CSK). Tyr-534 is one of the major phosphorylation sites and an increase in phosphorylation and Src kinase activity is associated with prostate cancer progression. Phosphorylation by TNK2 enhances the DNA-binding and transcriptional activity and may be responsible for androgen-independent progression of prostate cancer.
Target information above from: UniProt accession
P10275
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010)
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Alternative names
- AISANDR_HUMANAndrogen receptor
- ARDHTRDihydrotestosterone receptorHUMARAHYSP1KDNR3C4Nuclear receptor subfamily 3 group C member 4SBMASMAX1TFM
see all
- Entrez Gene: 403588 Dog
- Entrez Gene: 367 Human
- Omim: 313700 Human
- SwissProt: Q9TT90 Dog
- SwissProt: P10275 Human
- Unigene: 496240 Human
Applications
Our Abpromise guarantee covers the use of ab128498 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Notes |
|---|---|
| Sandwich ELISA | sELISA |
Androgen Receptor ELISA Kit images
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Monitoring protein expression levels of Androgen Receptor using ab128498.
Different amounts of nuclear extracts from three Human prostate cancer cell lines: LnCaP, PC-3 and DU145 were analyzed for levels of Androgen Receptor protein. This data is provided for demonstration only.
Protocols
References for Androgen Receptor ELISA Kit (ab128498)
ab128498 has not yet been referenced specifically in any publications.
