Comparison

Sheep A\&#039, Glucocorticoid Rec.

Item no. 18-511-244892
Manufacturer GENWAY
Amount 0,2 ml
Category
Type Antibody
Specific against Salmon (Salmo salar)
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-671893
Similar products 18-511-244892
Available
Genway ID:
GWB-671893
Host Animal:
Sheep
Immunogen:
Peptide consisting of amino acids 150-175 of squirrel monkey glucocortcoid receptor coupled to diptheria toxoid. This sequence is identical in human glucocorticoid receptor except for 2 amino acids (underlined): N terminus - APKEKEFPKTHSDVSSEQQNLKGQTG-NH2 - C terminus.
Specificity:
Glucocorticoid Receptor Monkey/Human
Specificity:
Reacts specifically with monkey and human glucocorticoid receptor
Type of Product:
Polyclonal Antibodies to Hormones and Steroids
Buffer:
Not applicableApplications Notes : Has been used successfully in Western blot assays (1:500-1:1 000 dilution) to identify human glucocorticoid receptor. Each laboratory should determine an optimum working titer for use in its particular application. Other applications have not been tested but use in such assays should not necessarily be excluded. Sheep A\' Glucocorticoid Rec. . Sheep Antibody to Glucocorticoid Receptor
Function:
Receptor for glucocorticoids (GC). Has a dual mode of action: as a transcription factor that binds to glucocorticoid response elements (GRE) and as a modulator of other transcription factors. Affects inflammatory responses cellular proliferation and differentiation in target tissues. Could act as a coactivator for STAT5-dependent transcription upon growth hormone (GH) stimulation and could reveal an essential role of hepatic GR in the control of body growth. Involved in chromatin remodeling. Plays a significant role in transactivation. Involved in nuclear translocation (By similarity).
Subunit:
Heteromultimeric cytoplasmic complex with HSP90 HSP70 and FKBP5 or another immunophilin or the immunophilin homolog PPP5C. Directly interacts with UNC45A. Upon ligand binding FKBP5 dissociates from the complex and FKBP4 takes its place thereby linking the complex to dynein and mediating transport to the nucleus where the complex dissociates (By similarity). Binds to DNA as a homodimer and as a heterodimer with NR3C2 or the retinoid X receptor. Binds STAT5A and STAT5B homodimers and heterodimers. Interacts with NRIP1 POU2F1 POU2F2 and TRIM28. Interacts with NCOA1 NCOA3 SMARCA4 SMARCC1 SMARCD1 and SMARCE1 (By similarity). Interacts with several coactivator complexes including the SMARCA4 complex CREBBP/EP300 TADA2L and p160 coactivators such as NCOA2 and NCOA6. Interaction with BAG1 inhibits transactivation. Interacts with HEXIM1 PELP1 and TGFB1I1.
Subcellular Location:
Cytoplasm. Nucleus. Note=Cytoplasmic in the absence of ligand nuclear after ligand-binding.
Tissue Specificity:
Widely expressed. In the heart detected in left and right atria left and right ventricles aorta apex intraventricular septum and atrioventricular node as well as whole adult and fetal heart.
Domain:
Composed of three domains: a modulating N-terminal domain a DNA-binding domain and a C-terminal steroid-binding domain.
Ptm:
Increased proteasome-mediated degradation in response to glucocorticoids.
Ptm:
Phosphorylated in the absence of hormone; becomes hyperphosphorylated in the presence of glucocorticoid. The Ser-203-phosphorylated form is mainly cytoplasmic and the Ser-211-phosphorylated form is nuclear. Transcriptional activity correlates with the amount of phosphorylation at Ser-211.
Ptm:
Sumoylated; this reduces transcription transactivation.
Ptm:
Ubiquitinated; restricts glucocorticoid-mediated transcriptional signaling (By similarity).
Polymorphism:
Carriers of the 22-Glu-Lys-23 allele are relatively more resistant to the effects of GCs with respect to the sensitivity of the adrenal feedback mechanism than non-carriers resulting in a better metabolic health profile. Carriers have a better survival than non-carriers as well as lower serum CRP levels. The 22-Glu-Lys-23 polymorphism is associated with a sex-specific beneficial body composition at young-adult age as well as greater muscle strength in males.
Disease:
Defects in NR3C1 are a cause of glucocorticoid resistance [MIM:138040]; also known as cortisol resistance. It is a hypertensive hyperandrogenic disorder characterized by increased serum cortisol concentrations. Inheritance is autosomal dominant.
Miscellaneous:
High constitutive expression of isoform beta by neutrophils may provide a mechanism by which these cells escape glucocorticoid-induced cell death. Up-regulation by proinflammatory cytokines such as IL8 further enhances their survival in the presence of glucocorticoids during inflammation.
Miscellaneous:
Can up- or down-modulate aggregation and nuclear localization of expanded polyglutamine polypeptides derived from AR and HD through specific regulation of gene expression. Aggregation and nuclear localization of expanded polyglutamine proteins are regulated cellular processes that can be modulated by this receptor a well-characterized transcriptional regulator.
Similarity:
Belongs to the nuclear hormone receptor family. NR3 subfamily.
Similarity:
Contains 1 nuclear receptor DNA-binding domain.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0,2 ml
Available: In stock
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