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anti-Human Adiponectin Receptor 1 Antikörper:
anti-Mouse (Murine) Adiponectin Receptor 1 Antikörper:
anti-Rat (Rattus) Adiponectin Receptor 1 Antikörper:
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Human Polyclonal Adiponectin Receptor 1 Primary Antibody für IF (p), IHC (p) - ABIN670836
Liu, Wu, Zhang, Chen, Liu, Wu, Zhu: The ameliorating effect of rosiglitazone on experimental nonalcoholic steatohepatitis is associated with regulating adiponectin receptor expression in rats. in European journal of pharmacology 2010
Show all 10 Pubmed References
Human Polyclonal Adiponectin Receptor 1 Primary Antibody für IHC (p), IHC - ABIN440478
Staiger, Kaltenbach, Staiger, Stefan, Fritsche, Guirguis, Péterfi, Weisser, Machicao, Stumvoll, Häring: Expression of adiponectin receptor mRNA in human skeletal muscle cells is related to in vivo parameters of glucose and lipid metabolism. in Diabetes 2004
Show all 6 Pubmed References
Human Polyclonal Adiponectin Receptor 1 Primary Antibody für IHC, WB - ABIN1169254
Corbetta, Redaelli, Pozzi, Bovo, Ratti, Redaelli, Pellegrini, Beck-Peccoz, Spada: Fibrosis is associated with adiponectin resistance in chronic hepatitis C virus infection. in European journal of clinical investigation 2011
Chicken Polyclonal Adiponectin Receptor 1 Primary Antibody für IHC, ELISA - ABIN1585580
Duivenvoorden, Paschos, Hopmans, Austin, Pinthus: Endoplasmic reticulum protein ERp46 in renal cell carcinoma. in PLoS ONE 2014
Broad Bean (Vicia faba) Polyclonal Adiponectin Receptor 1 Primary Antibody für IHC (p) - ABIN2477287
Shen, Li, Li, Wu, Ding: Pioglitazone prevents hyperglycemia induced decrease of AdipoR1 and AdipoR2 in coronary arteries and coronary VSMCs. in Molecular and cellular endocrinology 2012
Adiponectin and adiponectin receptor genes are coexpressed during zebrafish embryogenesis and regulated by food deprivation
Renoprotection of adiponectin is associated with improvement of the endothelial dysfunction, reduction of oxidative stress, and upregulation of endothelial nitric oxide synthase (zeige NOS3 Antikörper) expression through activation of adenosine 5'-monophosphate-activated protein kinase (zeige CDK7 Antikörper) by AdipoR1 and activation of peroxisome proliferator-activated receptor (zeige PPARD Antikörper) (PPAR)-alpha (zeige PPARA Antikörper) signaling pathway by AdipoR2 (zeige ADIPOR2 Antikörper). [review]
High ADIPOR1 expression is associated with breast cancer.
revised ADIPOR1 crystal structure exhibiting a seven-transmembrane-domain architecture that is clearly distinct from that of ADIPOR2 (zeige ADIPOR2 Antikörper)
TNF-alpha (zeige TNF Antikörper) impairs adiponectin/AdipoR1 signaling, mitochondrial biogenesis, and myogenesis in primary human myotubes cultures obtained from heart failure patients.
the knockdown phenotype was partially rescued by injecting wild-type, but not mutant, human ADIPOR1 mRNA. We conclude that ADIPOR1 is a novel adRP (zeige PLIN2 Antikörper)-causing gene and plays an important role in rod development and maintenance.
Adiponectin stimulates cPLA2 and COX-2 expression via AdipoR1/2-dependent activation of PKC/NADPH oxidase/mitochondria resulting in ROS accumulation, p300 phosphorylation, and histone H4 acetylation.
Decreased expression of ADIPOR1 is associated with polycystic ovary syndrome.
sequence- and structure-based computational tools were employed in this study to functionally and structurally characterize the coding Nonsynonymous Single Nucleotide Polymorphisms of ADIPOR1 gene listed in the single nucleotide polymorphisms database.
PCR results showed expression of adiponectin, AdipoR1, AdipoR2 (zeige ADIPOR2 Antikörper), follicle-stimulating hormone receptor (FSHR (zeige FSHR Antikörper)), and luteinizing hormone receptor (LHR (zeige LHCGR Antikörper)) in granulosa cells (GCs (zeige GCLC Antikörper)). After controlling body mass index (BMI) values, qRT-PCR demonstrated a decreased expression of adiponectin system in GCs (zeige GCLC Antikörper) of polycystic ovary syndromepatients compared to those in controls
ADPOR1 variants, rs3737884*G and rs7514221*C, may be shared risk factors associated with CAD (zeige CAD Antikörper), T2D, and T2D with CAD (zeige CAD Antikörper) in a population of northeast China.
This study demonstrated the presence of adiponectin and its receptors in the uteri, conceptuses, and trophoblasts of pregnant pigs and that the local adiponectin system is dependent on the stage of pregnancy.
Data suggest AdipoR1/adiponectin signaling up-regulates gene expression of hepatocyte enzymes involved in fatty acid metabolism and protects hepatocyte from nonesterified fatty acids by activating phosphatidylinositol 3-kinase (PI3K/AKT (zeige AKT1 Antikörper)) signaling.
study demonstrated that adiponectin and adiponectin receptors 1 and 2 messenger RNAs and proteins are present in the porcine hypothalamus and that their expression levels are determined by the pig's endocrine status related to the oestrous cycle
This study demonstrated the presence of adiponectin, AdipoR1 and AdipoR2 genes and proteins in the porcine uterus and the effect of the stage of the oestrous cycle on the expression of the adiponectin system.
Data indicate that AdipoR1 and AdipoR2 mRNAs and proteins are present in the porcine pituitary and that adiponectin receptors expression is dependent on endocrine status of the animals.
Results showed a high polymorphism of the ADIPOR1 and a complexity in its transcription level in longissimus dorsi from five pig breeds: Duroc, Polish Large White, Polish Landrace, Pietrain and Pulawska.
The cloning and characterization of adiponectin, ADIPOR1, and ADIPOR2 (zeige ADIPOR2 Antikörper) are reported.
FISH localization of 4 BAC clones harbouring potential candidate genes for fatness traits: DGAT1 (zeige DGAT1 Antikörper) (SSC4p15), PPARA (zeige PPARA Antikörper) (SSC5p15), ADIPOR1 (SSC10p13) and CREB (zeige CREB1 Antikörper) (SSC15q24)
Insulin regulates the expression of adiponectin and adiponectin receptors in porcine adipocytes.
Low level expression of adiponectin mRNA was found in all areas of bovine mammary gland tissues examined. AdipoR1 and AdipoR2 (zeige ADIPOR2 Antikörper) mRNAs were also detected in mammary tissues and their expression was particularly prominent in the parenchyma and cistern.
The physiologic status of the ovary has significant effects on the natural expression patterns of adiponectin and its receptors in follicular and luteal cells of bovine ovary.
adiponectin maintains intestinal homeostasis and protects against murine colitis through interactions with its receptor AdipoR1 and by modulating adaptive immunity and STAT3 (zeige STAT3 Antikörper) signaling
Based on these findings, this study showed that CTRP9 (zeige C1QTNF9 Antikörper) might induce mitochondrial biogenesis and protect high glucose-induced endothelial oxidative damage via AdipoR1-SIRT1 (zeige SIRT1 Antikörper)-PGC-1alpha (zeige PPARGC1A Antikörper) signaling pathway.
High salt is an important suppressor of cardioprotective APN (zeige ANPEP Antikörper) and AdipoR1 in cardiac myocytes.
AdipoR1, not AdipoR2 (zeige ADIPOR2 Antikörper), was first identified as a receptor of CTRP6 during the process of mitotic clonal expansion. Collectively, we suggest that CTRP6 mediates the ectopic lipogenesis through AdipoR1/Erk (zeige EPHB2 Antikörper)/PPARgamma (zeige PPARG Antikörper) signaling pathway in myoblasts.
The results demonstrated a dynamic dysfunction of APN (zeige ANPEP Antikörper)/AdipoR1 axis accompanying progression of diabetes mellitus in mice with cerebral ischemia.
physiologic adiponectin levels enhance the vasorelaxative response to acetylcholine by inducing nitric oxide production through AdipoR1/Cav-1 (zeige CAV1 Antikörper) mediated signaling.
AdipoR1 is expressed on adipose tissue-resident Tregs, mainly Helios (zeige ZNFN1A2 Antikörper)(+) Tregs, and this expression is dependent on weight and fat accumulation. This data proposes a new mechanism through which weight gain might alter immunoregulation.
Adiponectin directly acts on murine dermal gammadelta-T cells to suppress IL-17 (zeige IL17A Antikörper) synthesis via AdipoR1.
At high glucose concentrations in vitro, AdipoR1 regulated the survival of neural stem cells through the p53 (zeige TP53 Antikörper)/p21 (zeige D4S234E Antikörper) pathway and the proliferation- and differentiation-related factors of neural stem cells via TLX (zeige NR2E1 Antikörper).
Electroacupuncture induces protective effects against cerebral ischemia through AdipoR1-mediated phosphorylation of GSK-3Beta (zeige GSK3b Antikörper).
This gene encodes a protein which acts as a receptor for adiponectin, a hormone secreted by adipocytes which regulates fatty acid catabolism and glucose levels. Binding of adiponectin to the encoded protein results in activation of an AMP-activated kinase signaling pathway which affects levels of fatty acid oxidation and insulin sensitivity. A pseudogene of this gene is located on chromosome 14.
adiponectin receptor 1
, adiponectin receptor type I
, adiponectin receptor protein 1-like
, adiponectin receptor protein 1
, progestin and adipoQ receptor family member I