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anti-Human Angiotensin I Converting Enzyme 2 Antikörper:
anti-Mouse (Murine) Angiotensin I Converting Enzyme 2 Antikörper:
anti-Rat (Rattus) Angiotensin I Converting Enzyme 2 Antikörper:
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Human Monoclonal Angiotensin I Converting Enzyme 2 Primary Antibody für WB - ABIN1882190
Itoyama, Keicho, Hijikata, Quy, Phi, Long, Ha, Ban, Matsushita, Yanai, Kirikae, Kirikae, Kuratsuji, Sasazuki: Identification of an alternative 5'-untranslated exon and new polymorphisms of angiotensin-converting enzyme 2 gene: lack of association with SARS in the Vietnamese population. in American journal of medical genetics. Part A 2005
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Human Polyclonal Angiotensin I Converting Enzyme 2 Primary Antibody für IHC, IHC (p) - ABIN4277591
Lee, Nam, Park, Kim, Lafleur, Aburatani, Yang, Kim, Goldenring: Gene expression profiling of metaplastic lineages identifies CDH17 as a prognostic marker in early stage gastric cancer. in Gastroenterology 2010
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Human Polyclonal Angiotensin I Converting Enzyme 2 Primary Antibody für ELISA, WB - ABIN1169446
Beniac, deVarennes, Andonov, He, Booth: Conformational reorganization of the SARS coronavirus spike following receptor binding: implications for membrane fusion. in PLoS ONE 2007
Human Monoclonal Angiotensin I Converting Enzyme 2 Primary Antibody für FACS, ELISA - ABIN1169449
Zulli, Rai, Buxton, Burrell, Hare: Co-localization of angiotensin-converting enzyme 2-, octomer-4- and CD34-positive cells in rabbit atherosclerotic plaques. in Experimental physiology 2008
Human Polyclonal Angiotensin I Converting Enzyme 2 Primary Antibody für FACS, IF (p) - ABIN730798
Raffai, Khang, Vanhoutte: Angiotensin-(1-7) augments endothelium-dependent relaxations of porcine coronary arteries to bradykinin by inhibiting angiotensin-converting enzyme 1. in Journal of cardiovascular pharmacology 2014
Human Polyclonal Angiotensin I Converting Enzyme 2 Primary Antibody für ELISA, ICC - ABIN4277590
Wang, Liang, Leung: The ACE2/Ang-(1-7)/Mas Axis Regulates the Development of Pancreatic Endocrine Cells in Mouse Embryos. in PLoS ONE 2015
Cow (Bovine) Polyclonal Angiotensin I Converting Enzyme 2 Primary Antibody für IHC, WB - ABIN2774060
Haga, Yamamoto, Nakai-Murakami, Osawa, Tokunaga, Sata, Yamamoto, Sasazuki, Ishizaka: Modulation of TNF-alpha-converting enzyme by the spike protein of SARS-CoV and ACE2 induces TNF-alpha production and facilitates viral entry. in Proceedings of the National Academy of Sciences of the United States of America 2008
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results suggest that ACE2, TNNI3K and CALM3 polymorphisms are associated with increased risk of hypertrophic cardiomyopathies and dilated cardiomyopathies and may act as disease modifiers of these diseases.
Elevated plasma ACE2 is significantly associated with more advanced LA structural remodeling in atrial fibrillation.
Overexpression of ACE2 in monocytes led to reduced endothelial adhesion, transmigration and downregulation of adhesion-related molecules and results in atherosclerosis.
These results indicated that aberrant methylation of the ACE2 promoter may be associated with EH risk. In addition, sex may significantly influence ACE2 methylation.
ACE2 rs2106809 is an important predictive factor of the response to antihypertensive treatment with ACE (zeige ACE Antikörper) inhibitors in Chinese female hypertensive patients.
In islets from db/db (zeige LEPR Antikörper) mice, ACE2 over-expression increased intracellular calcium influx and restored impaired mitochondrial oxidation, potentially causing an increase in GSIS. These results shed light on the potential roles of ACE2 in mitochondrial metabolism, moreover, may improve our understanding of diabetes.
ACE2 may have a role in silent atherosclerosis in patients with chronic kidney disease; it counterbalances the vasoconstrictor adverse effects of angiotensin II by its conversion
This study reveals an elevated serum concentration of ACE2 and independent associations between serum ACE2 and echocardiographic parameters in hypertensive patients.
The findings of this study indicate that ACE-2 activity is reduced in AD and is an important regulator of the central classical ACE-1 (zeige ACE Antikörper)/Ang II (zeige AGT Antikörper)/AT1R (zeige AGTR1 Antikörper) axis of renin (zeige REN Antikörper)-angiotensin system, and also that dysregulation of this pathway likely plays a significant role in the pathogenesis of Alzheimer's disease.
Overexpression of ACE2 ameliorates Abeta (zeige APP Antikörper)-induced inflammatory response by activating the ACE2/Ang-(1 (zeige ANGPT1 Antikörper)-7)/Mas (zeige MAS1 Antikörper) axis in human RPE (zeige RPE Antikörper) cells.
These results were supported by the opposite outcomes observed for cells treated with A779 or DX600. Therefore, it was concluded that the ACE2-Ang (zeige ANG Antikörper)(17)-Mas (zeige MAS1 Antikörper) axis significantly inhibits pancreatitis by inhibition of the p38 MAPK (zeige MAPK14 Antikörper)/NF-kappaB (zeige NFKB1 Antikörper) signaling pathway
Exogenous ACE2 alters angiotensin peptide metabolism in the kidneys of Col4a3 (zeige COL4a3 Antikörper) knockout mice and attenuates the progression of Alport syndrome nephropathy.
Profound augmentation of ACE2 confined to the circulation failed to ameliorate the glomerular lesions and hyperfiltration characteristic of early diabetic nephropathy.
Nrf2-mediated stimulation of intrarenal Renin-Angiotensin syste, (CAE2 and MasR) gene expression, by which chronic hyperglycemia induces hypertension and renal injury in diabetes.
Ultra-high doses did not influence the ACE2/AT2R (zeige AGTR2 Antikörper)/Mas (zeige MAS1 Antikörper) axis and promoted renal injury with increased renal ERK1/2 activation and exaggerated fibronectin (zeige FN1 Antikörper) expression in db/db (zeige LEPR Antikörper) mice. Our study demonstrates dose-related effects of candesartan in diabetic nephropathy: intermediate-high dose candesartan is renoprotective, whereas ultra-high dose candesartan induces renal damage.
Altogether, our study demonstrates that HFD feeding increases RAS activity and mediates glycemic dysregulation likely through loss of ACE2 present outside the islets but independently of changes in islet ACE2.
Results suggest that angiotensin converting enzyme 2 may reduce anxiety-like behavior by activating central Mas (zeige MAS1 Antikörper) receptor that facilitate GABA release onto pyramidal neurons within the basolateral amygdala.
These findings demonstrate that ACE2 plays a critical role in preventing RSV-induced lung injury, and suggest that ACE2 is a promising potential therapeutic target in the management of RSV-induced lung disease.
ACE2 overexpression significantly reduced the myocardial infarction-induced increase in apoptosis, macrophage infiltration, and HMGB1 (zeige HMGB1 Antikörper) and proinflammatory cytokine expression.
The objective of this study was to characterize the profiles of Ang-(1-7), MAS receptor, ACE(2), NEP and PEP during the ovulatory process in cattle.
sporadic non-synonymous substitutions reduced the level of rh-ACE2 protein expression and did not support severe acute respiratory syndrome coronavirus entry effectively
In a pig model of acute pulmonary embolism leading to cardiac arrest, captopril infusion was associated with less mean right ventricular pressure overload after resuscitation, compared with saline infusion. The reduction in systemic and pulmonary vascular resistance associated with captopril may be by inhibiting the ACE (zeige ACE Antikörper)-Ang II (zeige AGT Antikörper)-AT1R (zeige AGTR1 Antikörper) axis and activating the ACE2/Ang-(1 (zeige ANGPT1 Antikörper)-7)/Mas (zeige MAS1 Antikörper) axis.
This study produced the full-length porcine ACE2 cDNA sequence and found polyunsaturated fatty acids could downregulate the expression of ACE2.
activation of the central rennin-angiotensin system in animals with chronic heart failure involves an imbalance of ACE (zeige ACE Antikörper) and ACE2 in regions of the brain that regulate autonomic function.
Overexpression of ACE2 inhibited atherosclerotic plaque inflammation response in hypercholesterolemic rabbits.
The protein encoded by this gene belongs to the angiotensin-converting enzyme family of dipeptidyl carboxydipeptidases and has considerable homology to human angiotensin 1 converting enzyme. This secreted protein catalyzes the cleavage of angiotensin I into angiotensin 1-9, and angiotensin II into the vasodilator angiotensin 1-7. The organ- and cell-specific expression of this gene suggests that it may play a role in the regulation of cardiovascular and renal function, as well as fertility. In addition, the encoded protein is a functional receptor for the spike glycoprotein of the human coronaviruses SARS and HCoV-NL63.
, angiotensin I converting enzyme (peptidyl-dipeptidase A) 2
, angiotensin-converting enzyme 2
, angiotensin-converting enzyme homolog
, metalloprotease MPROT15
, peptidyl-dipeptidase A
, angiotensin I converting enzyme 2
, anigotensin-converting enzyme-related carboxypeptidase
, renal angiotensin-converting enzyme 2