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Human Monoclonal NR1H4 Primary Antibody für IF, ELISA - ABIN523347
Chen, Song, Valanejad, Vasilenko, More, Qiu, Chen, Lai, Slitt, Stoner, Yan, Deng: Bile salt export pump is dysregulated with altered farnesoid X receptor isoform expression in patients with hepatocellular carcinoma. in Hepatology (Baltimore, Md.) 2013
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Human Polyclonal NR1H4 Primary Antibody für IF (p), IHC (p) - ABIN1714781
Yang, Mei, Xu, Zhou, Zhu, Sun, Huang, Wang, Shu, Liu, Ding, Hassan, Zhang, Jiang: Early indications of ANIT-induced cholestatic liver injury: Alteration of hepatocyte polarization and bile acid homeostasis. in Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 2018
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Human Polyclonal NR1H4 Primary Antibody für ELISA, WB - ABIN188692
Huang, Ma, Zhang, Qatanani, Cuvillier, Liu, Dong, Huang, Moore: Nuclear receptor-dependent bile acid signaling is required for normal liver regeneration. in Science (New York, N.Y.) 2006
Human Polyclonal NR1H4 Primary Antibody für ICC, IF - ABIN152921
Xing, Saner-Amigh, Nakamura, Hinshelwood, Carr, Mason, Rainey: The farnesoid X receptor regulates transcription of 3beta-hydroxysteroid dehydrogenase type 2 in human adrenal cells. in Molecular and cellular endocrinology 2009
Human Polyclonal NR1H4 Primary Antibody für WB - ABIN4312873
Lian, Wang, Xiao, Wu, Xu, Liang, Yang: Activated farnesoid X receptor attenuates apoptosis and liver injury in autoimmune hepatitis. in Molecular medicine reports 2015
Cow (Bovine) Polyclonal NR1H4 Primary Antibody für WB - ABIN2773865
Kaeding, Bouchaert, Bélanger, Caron, Chouinard, Verreault, Larouche, Pelletier, Staels, Bélanger, Barbier: Activators of the farnesoid X receptor negatively regulate androgen glucuronidation in human prostate cancer LNCAP cells. in The Biochemical journal 2008
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Loss of FXR or its down-regulation is associated with higher bile acids concentrations and with a pro-tumorigenic phenotype. (Review)
Lys (zeige LYZ Antikörper)-325 is a non-canonical site of SUMOylation of human FXR.CK2 is the priming effector that phosphorylates Ser (zeige SIGLEC1 Antikörper)-327, resulting in enhanced SUMO2 (zeige SUMO2 Antikörper) conjugation, which then directs the ubiquitination and degradation of FXR through the recruitment of the SUMO-dependent ubiquitin E3 ligase RNF4 (zeige RNF4 Antikörper).
we proposed a model to link FXR to Sp1 (zeige PSG1 Antikörper), which included triggered FXR, p38/MAPK (zeige MAPK14 Antikörper) and/or PI3K (zeige PIK3CA Antikörper)/AKT (zeige AKT1 Antikörper) signaling and phosphorylated Sp1 (zeige PSG1 Antikörper), to illustrate the potential crosstalk between the two factors.
the presented evidence suggested that WA can inhibit HCC (zeige FAM126A Antikörper) cell proliferationand tumorigenesis through miR (zeige MLXIP Antikörper)-22-repressed CCNA2 (zeige CCNA2 Antikörper), which was at least partially through FXR regulation
The results indicated that epigenetically regulated miR (zeige MLXIP Antikörper)-449a targets CREB5 (zeige CREB5 Antikörper) to increase FXRalpha expression, thereby promoting HBV replication and gene expression. Our findings provide a new understanding of the role of miRNAs in HBV replication
In diabetic humans, there is decreased FXR expression in the kidney. FXR plays an important role in Diabetic Kidney Disease.
FXR regulates serum triglyceride level in part through PLA2G12B (zeige PLA2G12B Antikörper).
we conclude that FXR-Gank (zeige PSMD10 Antikörper)-TSPs-Stem cells pathway is a key determinant of liver cancer in animal models and in pediatric liver cancer. Our data provide a strong basis for development of FXR-Gank (zeige PSMD10 Antikörper)-based therapy for treatment of patients with hepatoblastoma
PPARalpha (zeige PPARA Antikörper) and FXR function coordinately to integrate liver energy balance.
These studies investigated in differentiated HepaRG cells and in primary human hepatocytes (PHHs) effects of FXR activation on HBV replication and of infection on the FXR pathway.
results suggest that hypothyroidism induces a moderate non-alcoholic steatohepatitis, alllowing the hepatic regeneration. The FXRalpha may be involved in the development of non-alcoholic steatohepatitis in hypothyroid subjects.
FXR is expressed in the ovary, in all regions of the oviduct, and all portions of the vagina of rabbits.
FXR signaling is a bile acid nuclear receptor that regulates lipids and glucose homeostasis and lack of it causes hepatomegaly and liver dysfunction.
These results suggest that lack of FXR impaired FoxO3a (zeige FOXO3 Antikörper)-mediated autophagy and in turn exacerbated alcohol-induced liver injury
Bile acids and salts (BA) treatment-farnesoid X-activated receptor (FRXalpha) signaling is a critical actor during sexual maturation.
The study shows that FXR/RXR regulates Chop (zeige DDIT3 Antikörper) expression in a mouse model of steatohepatitis, providing novel insights into pathogenesis of this disorder.
FXR activation ameliorated central nervous system autoimmunity in an IL-10 (zeige IL10 Antikörper)-dependent fashion and even suppressed advanced clinical disease upon therapeutic administration
In livers of mice, FXR regulates amino acid catabolism and detoxification of ammonium via ureagenesis and glutamine (zeige GFPT1 Antikörper) synthesis.
Data suggest that FXR and TGR5 (zeige GPBAR1 Antikörper) expression is down-regulated in aging kidney; caloric restriction prevents these age-related changes. Additionally, in long-lived Ames dwarf (zeige PROP1 Antikörper) mice, renal FXR and TGR5 (zeige GPBAR1 Antikörper) expression is up-regulated. Treatment of aged mice with dual FXR/TGR5 (zeige GPBAR1 Antikörper) agonist reverses age-related changes in kidney structure/function. (FXR = farnesoid X activated receptor; TGR5 (zeige GPBAR1 Antikörper) = G protein-coupled bile acid receptor 1 (zeige GPBAR1 Antikörper))
this study provides evidence for roles of FXR as an important regulator of placental inflammation
These findings suggest that bile acids and FXR play pivotal roles in sepsis via controlling the NLRP3 (zeige NLRP3 Antikörper) inflammasome.
alterations in bile acid composition may have contributed to the observed disturbance in FXR-mediated signalling pathways in short bowel syndrome-associated liver disease
FXR splice variant has a dominant positive effect on wild type FXR.
In conclusion, PXR (zeige NR1I2 Antikörper) and FXR both responded to ligands that activated their human orthologs, and some of the alternatively spliced variants significantly altered PXR (zeige NR1I2 Antikörper) and FXR transactivation at in vivo expression levels.
This gene encodes a ligand-activated transcription factor, which shares structural features in common with nuclear hormone receptor family, such as a DNA-binding domain that targets the receptor to specific DNA sequences, and a ligand-binding domain, which interacts directly with the ligand and contains a ligand-dependent transcriptional activation domain. This protein functions as a receptor for bile acids, and when bound to bile acids, regulates the expression of genes involved in bile acid synthesis and transport. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
nuclear receptor subfamily 1, group H, member 4
, orphan nuclear receptor FOR2
, bile acid receptor
, farnesoid X activated receptor
, bile acid receptor-like
, RXR-interacting protein 14
, farnesoid X nuclear receptor
, farnesoid X-activated receptor
, farnesol receptor HRR-1
, retinoid X receptor-interacting protein 14
, nuclear receptor subfamily 1 group H member 4