Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Wählen Sie die Spezies und Applikation aus
anti-Rat (Rattus) Antikörper:
anti-Mouse (Murine) Antikörper:
Sie gelangen zu unserer vorgefilterten Suche.
Guinea Pig Monoclonal NR3C1 Primary Antibody für BP, ChIP - ABIN268501
Lambert, Nordeen: CBP recruitment and histone acetylation in differential gene induction by glucocorticoids and progestins. in Molecular endocrinology (Baltimore, Md.) 2003
Show all 7 Pubmed References
Human Monoclonal NR3C1 Primary Antibody für WB - ABIN1882199
Wang, Shen, Thiyagarajan, Lin, Palm, Horvath, Klopstock, Cutler, Pique, Schrijver, Davis, Mindrinos, Speed, Scharfe: Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing. in Nucleic acids research 2011
Show all 4 Pubmed References
Human Monoclonal NR3C1 Primary Antibody für ICC, FACS - ABIN969321
Charmandari, Ichijo, Jubiz, Baid, Zachman, Chrousos, Kino: A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene enhancing hGR-mediated gene expression. in The Journal of clinical endocrinology and metabolism 2008
Show all 2 Pubmed References
Human Monoclonal NR3C1 Primary Antibody für ELISA, WB - ABIN2473809
Harris, Kerns, St Clair: RNA sulfurtransferase activity in rat liver and chemically induced hepatomas. in Cancer research 1976
Show all 4 Pubmed References
Cow (Bovine) Polyclonal NR3C1 Primary Antibody für ChIP, ICC - ABIN152763
He, Simons: STAMP, a novel predicted factor assisting TIF2 actions in glucocorticoid receptor-mediated induction and repression. in Molecular and cellular biology 2007
Human Polyclonal NR3C1 Primary Antibody für IF (p), IHC (p) - ABIN685138
Ding, Shi, Han, Cui: Regulation of glucocorticoid-related genes and receptors/regulatory enzyme expression in intrauterine growth restriction filial rats. in Life sciences 2016
Human Polyclonal NR3C1 Primary Antibody für ChIP, ICC - ABIN152786
Liang, Kowalczyk, Junco, Klug-De Santiago, Malik, Wei, Slaga: Differential effects on lung cancer cell proliferation by agonists of glucocorticoid and PPARα receptors. in Molecular carcinogenesis 2014
Human Polyclonal NR3C1 Primary Antibody für FACS, IF (p) - ABIN726875
Takigawa, Miyazaki, Kinoshita, Kawarabayashi, Nishiyama, Hatsuse, Ono, Saitoh, Seki, Yamamoto: Glucocorticoid receptor-dependent immunomodulatory effect of ursodeoxycholic acid on liver lymphocytes in mice. in American journal of physiology. Gastrointestinal and liver physiology 2013
Human Polyclonal NR3C1 Primary Antibody für WB - ABIN2792573
: Triazolam Effects On Explicit Memory, Implicit Memory and Metamemory: Lister RG, Joyce EM, Weingartner HJ, Eckardt MJ Laboratory of Clinical Studies, NIAAA, DICBR, Bldg 10 Rm 3C102, 9000 Rockville Pike, Bethesda, MD 20892, USA. in Journal of psychopharmacology (Oxford, England) 2012
Opn4m2 (zeige OPN4 Antikörper) labeling shows nuclear localization, which did not change in response to light. opn4m1 (zeige OPN4 Antikörper), opn4m2 (zeige OPN4 Antikörper), gr, per1b, and cry1b presented an oscillatory profile of expression in LD condition. In both DD and LD condition, dexamethasone (DEX) treatment shifted the peak expression of per1b and cry1b transcripts
Data (including data from studies in knockout/transgenic mice) suggest that, under hypoxic conditions, muscle atrophy and elevated gene expression of ubiquitin proteasomal system-associated enzymes are mostly independent of glucocorticoid/Nr3c1 signaling.
We propose that the GC-induced mitochondrial accumulation of Bax (zeige BAX Antikörper) and the interaction between the GR and Bim (zeige BCL2L11 Antikörper), Bcl-xL (zeige BCL2L1 Antikörper) and Bak (zeige BAK1 Antikörper) could play a role in the regulation of thymocyte apoptosis.
The potentiation of RANKL (zeige TNFSF11 Antikörper) induced CTX release by dexamethasone was significantly less in bone marrow macrophage cells from mice with conditional knockout of the osteoclastic glucocorticoid receptor and completely absent in cells from GR(dim) mice, which carry a point mutation in one dimerizing interface of the GC receptor.
These data establish SUMO conjugation as a novel regulatory mechanism in the Hsp90 (zeige HSP90 Antikörper) cochaperone activity of FKBP51 (zeige FKBP5 Antikörper) with a functional impact on GR signaling in a neuronal context.
These results together suggested that ERK1 (zeige MAPK3 Antikörper) phosphorylation plays a critical role in regulating GR beta expression and hydrocortisone-induce GR phosphorylation at Ser220, which is critical for the anti-apoptotic effects hydrocortisone on hepatic ischemia-reperfusion injury.
a significant protein-protein interaction between GR and CHOP (zeige DDIT3 Antikörper), (GR-CHOP (zeige DDIT3 Antikörper) heterocomplex formation) under endoplasmic reticulum stress conditions, is reported.
This study identifies an endocrine developmental axis in which fetal GR primes the activity of PPARalpha (zeige PPARA Antikörper) in anticipation of the sudden shifts in postnatal nutrient source and metabolic demands.
Skin differentiation is impaired, and both apoptosis and cell proliferation are augmented in the absence of p23 (zeige CDK5R1 Antikörper); the consequences are a severe thinning of the stratum corneum and reduced numbers of hair follicles. Since the phenotype of p23 (zeige CDK5R1 Antikörper)-null embryos is strikingly similar to that of embryos lacking the glucocorticoid receptor, a paradigmatic Hsp90 (zeige HSP90 Antikörper)-p23 (zeige CDK5R1 Antikörper) client protein, we investigated glucocorticoid signaling.
REV-ERBalpha (zeige NR1D1 Antikörper) binds to the C-terminal portion and GR to the N-terminal portion of HSP90alpha (zeige HSP90AA2 Antikörper) and HSP90beta (zeige HSP90AB1 Antikörper), a chaperone responsible for the activation of proteins to ensure survival of a cell.
Phospho-AMPK (zeige PRKAA1 Antikörper) is a molecular switch able to cooperate with glucocorticoid receptors and Ppar-alpha (zeige PPARA Antikörper) at the chromatin level, a novel adaptation mechanism to prolonged fasting.
The guinea pig GR-specific mutations within the H1-H3 loop confer global changes within the GR-Hsp90 (zeige HSP90 Antikörper) complex that favor FKBP51 (zeige FKBP5 Antikörper) repression over FKBP52 (zeige FKBP4 Antikörper) potentiation.
Here we show genome-wide that blocked GBR generally require CHD9 (zeige CHD9 Antikörper) and BRM (zeige SMARCA2 Antikörper) for GR occupancy in contrast to GBR that are not blocked by Hic-5 (zeige TGFB1I1 Antikörper). Hic-5 (zeige TGFB1I1 Antikörper) blocked GBR are enriched near Hic-5 (zeige TGFB1I1 Antikörper) blocked GR target genes but not near GR target genes that are not blocked by Hic-5 (zeige TGFB1I1 Antikörper).
There was no significant association between different genotypes and alleles of Glucocorticoid Receptor of rs6195, rs6189/rs6190 variants, and response to fluoxetine (p=0.213 and 0.99, respectively).
NR3C1 gene polymorphisms are significantly associated with the response to glucocorticoids.
There is no clear evidence that the analysed NR3C1 allelic variants confer a risk for developing systemic autoimmune diseases although the minor G allele of rs41423247 may be protective among Caucasians (review and meta-analysis).
Analyses demonstrated a trend in the association between maternal trait anxiety and depression symptoms with placental gene expression of NR3C1. We found a significant interaction with maternal ethnicity. In Caucasians only, prenatal trait anxiety and depressive symptoms were associated with an increase in placental NR3C1 expression, and prenatal life events were associated with a down regulation of HSD11B2 (zeige HSD11B2 Antikörper)
We genotyped 10 single nucleotide polymorphisms (SNPs) on the NR3C1 gene (rs10482682, rs33389, rs10482633, rs10515522, rs2963156, rs4128428, rs9324918, rs41423247, rs6189, rs10052957).Haplotype analyses revealed significant effects of NR3C1 (p = 0.011) on cortisol stress response. Neither NR3C1 haplotype nor NR3C2 (zeige NR3C2 Antikörper) haplotype was associated with reasoning abilities.
In this study, we described the cellular localization of the glucocorticoid receptor in the human adult and fetal testis and provided evidence of an association between semen quality and a genetic polymorphism BclI (rs41423247) in the NR3C1 gene.
Results indicate that maltreated children evidence higher baseline levels of NR3C1 methylation, significant decreases in methylation over time, and then at follow-up, lower levels of methylation, relative to nonmaltreated preschoolers.
children with early onset maltreatment evidence significant hypermethylation compared to nonmaltreated children. Also, hypermethylation of NR3C1 is linked with a number of negative child outcomes including greater emotional lability-negativity, higher levels of ego undercontrol, more externalizing behavior, and greater depressive symptoms.
Study evaluated whether associations between early adversity and brain responses to dynamic facial expressions in early adulthood varied as a function of regional differences in the expression of NR3C1. Strongest associations between adversities and BOLD response to fearful faces were in brain regions with higher NR3C1 mRNA expression levels. Highest expression of NR3C1 is found in occipital and lowest in temporal regions
These results indicate that myostatin (zeige MSTN Antikörper) mediates maternal low protein diet-induced growth retardation, through epigenetic regulation involving FoxO3 (zeige FOXO3 Antikörper) and glucocorticoid receptor binding to its promoter.
Data indicate that higher hepatic glucocorticoid receptor (GR) expression in EHL piglets attributes mainly to the enhanced transcription of GR promoter 1-9/10 from breed-specific interaction of p53 (zeige TP53 Antikörper) and specificity protein 1 (Sp1 (zeige SP1 Antikörper)).
Tissue specificities, gene expression and induction responsiveness of the porcine NR3C1 gene.
Cloning and dna sequence analysis of the upstream flanking region of the NR3C1 gene in the domestic pig.
Effects of age, weaning and/or social isolation on the expression of genes regulating glucocorticoid response [glucocorticoid receptor).
Glucocorticoid Receptor protein expression in granulosa cells was higher in cysts from animals with spontaneous cystic ovarian disease and adrenocorticotropic hormone-induced cystic ovarian disease than in tertiary follicles from control animals.
Exposure to follicular fluid transiently increased the transcript levels of IL8 (zeige IL8 Antikörper) and PTGS2 (zeige PTGS2 Antikörper), and decreased the expression of SOD2 (zeige SOD2 Antikörper), GPX3 (zeige GPX3 Antikörper), DAB2 (zeige DAB2 Antikörper), and NR3C1. TNF (zeige TNF Antikörper) and IL6 (zeige IL6 Antikörper) levels were also decreased while those of NAMPT (zeige NAMPT Antikörper) were unaffected.
Bayesian image analysis of dexamethasone and shear stress-induced glucocorticoid receptor intracellular movement
investigation of gene expression for GR, 11HSD1, and 11HSD2 (zeige HSD11B2 Antikörper) in granulosa cells and theca interna layers during follicular maturation and atresia: expression of GR was largely unchanged during follicular maturation
The E domain of the trout receptors are not involved in the nucleocytoplasmic localization of naive trout GRs (zeige GARS Antikörper), but the A/B domain, especially if linked to the corresponding trout CD region, plays a pivotal role in the cellular distribution pattern.
This gene encodes glucocorticoid receptor, which can function both as a transcription factor that binds to glucocorticoid response elements in the promoters of glucocorticoid responsive genes to activate their transcription, and as a regulator of other transcription factors. This receptor is typically found in the cytoplasm, but upon ligand binding, is transported into the nucleus. It is involved in inflammatory responses, cellular proliferation, and differentiation in target tissues. Mutations in this gene are associated with generalized glucocorticoid resistance. Alternative splicing of this gene results in transcript variants encoding either the same or different isoforms. Additional isoforms resulting from the use of alternate in-frame translation initiation sites have also been described, and shown to be functional, displaying diverse cytoplasm-to-nucleus trafficking patterns and distinct transcriptional activities (PMID:15866175).
, nuclear receptor subfamily 3, group C, member 1
, glucocorticoid receptor 1
, nuclear receptor subfamily 3 group C member 1
, glucocorticoid nuclear receptor variant 1
, glucocorticoid receptor alpha
, glucocorticoid receptor variant P
, glucocorticoid receptor variant beta
, glucocorticoid receptor variant gamma