Vergleich

ANDROGEN RECEPTOR

ArtNr 18-783-77236
Hersteller GENWAY
Menge 1 ml
Kategorie
Typ Antibody
Applikationen IHC
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-C84FC6
Similar products 18-783-77236
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Genway ID:
GWB-C84FC6
Specificity:
ANDROGEN RECEPTOR
Isotype:
Polyclonal IgGTarget Species: HumanPeptide
Sequence:
S-T-E-D-T-A-E-Y-S-P-F-K-G-G-Y-T-K
Immunogen:
Synthetic peptide corresponding to the amino acids 1242 - 1255 of the native molecule conjugated to Keyhole limpet Haemocyanin.
Specificity Note:
This product is specific for Androgen Receptor (AR). Dihydrotestosterone (DHT) binds with highest affinity to AR and together with testosterone promotes AR transcriptional activity thereby ensuring the development and maintenance of male reproductive functions. AR homodimers recruit a variety of factors including coactivators and mediator proteins whose enzymatic activities promote chromatin remodeling and transcriptional regulation of target genes leading to cell differentiation survival and proliferation. Mutated AR is strongly implicated in development of prostate adenocarcinoma and metastases development. AR mutations can also cause spinal bulbar muscular atrophy (Kennedy disease) and partial/ complete androgen insensitivity. IHC: This product does not require protein digestion pre-treatment or antigen retrieval using heat treatment prior to staining of paraffin sections.
Preparation:
Purified IgG prepared by affinity chromatography
Buffer Solution:
Phosphate buffered saline pH 7. 2
Preservative Stabilisers:
0. 09% Sodium Azide (NaN3)
Function:
The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Activated but not phosphorylated by HIPK3.
Subunit:
Binds DNA as a homodimer. Part of a ternary complex containing AR EFCAB6/DJBP and PARK7. Interacts with HIPK3 in the presence of androgen. The ligand binding domain interacts with MYST2/HBO1 in the presence of dihydrotestosterone. Interacts with EFCAB6/DJBP PELP1 PQBP1 RANBP9 SPDEF SRA1 TGFB1I1 ZNF318 and RREB1. The AR N-terminal poly-Gln region binds Ran resulting in enhancement of AR-mediated transactivation. Ran-binding decreases as the poly-Gln length increases. Interacts with ZMIZ1/ZIMP10 and ZMIZ2/ZMIP7 which both enhance its transactivation activity (By similarity). Interacts with SLC30A9 and RAD54L2/ARIP4.
Subcellular Location:
Nucleus.
Domain:
Composed of three domains: a modulating N-terminal domain a DNA-binding domain and a C-terminal steroid-binding domain. Interaction with RANBP9 is mediated by both the N-terminal domain and the DNA-binding domain. Interaction with EFCAB6/DJBP is mediated by the DNA-binding domain (By similarity).
Ptm:
Phosphorylated in prostate cancer cells in response to several growth factors including EGF. Phosphorylation is induced by c-Src kinase (CSK). Tyr-514 is one of the major phosphorylation sites and an increase in phosphorylation and Src kinase activity is associated with prostate cancer progression (By similarity).
Miscellaneous:
In the absence of ligand steroid hormone receptors are thought to be weakly associated with nuclear components; hormone binding greatly increases receptor affinity. The hormone-receptor complex appears to recognize discrete DNA sequences upstream of transcriptional start sites.
Miscellaneous:
Transcriptional activity is enhanced by binding to RANBP9.
Similarity:
Belongs to the nuclear hormone receptor family. NR3 subfamily.
Similarity:
Contains 1 nuclear receptor DNA-binding domain.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 1 ml
Lieferbar: In stock
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Lieferung vsl. bis 27.09.2024 

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