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anti-Human MAS1 Antibodies:
anti-Mouse (Murine) MAS1 Antibodies:
anti-Rat (Rattus) MAS1 Antibodies:
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Cow (Bovine) Polyclonal MAS1 Primary Antibody for IHC, WB - ABIN2784456
Santos, Simoes e Silva, Maric, Silva, Machado, de Buhr, Heringer-Walther, Pinheiro, Lopes, Bader, Mendes, Lemos, Campagnole-Santos, Schultheiss, Speth, Walther: Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor Mas. in Proceedings of the National Academy of Sciences of the United States of America 2003
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.
Ang-(1 (show ANGPT1 Antibodies)-7) downregulated AT1R (show AGTR1 Antibodies) mRNA, upregulated mRNA levels of Ang II (show AGT Antibodies) type 2 receptor (AT2R (show AGTR2 Antibodies)) and Mas receptor (MasR) and p38-MAPK (show MAPK14 Antibodies) phosphorylation and suppressed H22 cell-endothelial cell communication
MAS1 might act as an inhibitory regulator of breast cancer.
Data show that MAS receptor exhibited constitutive activity that was inhibited by the non-peptide inverse agonist.
Data suggest that angiotensin converting enzyme 2 (show ACE2 Antibodies)/angiotensin II-(1-7)/MAS1 axis regulates leukocyte recruitment/activation, cell proliferation, and inflammation/fibrosis; main topic here is kidney/inflammatory renal disease. [REVIEW]
Up-regulation of the ACE2 (show ACE2 Antibodies)/Ang-(1 (show ANGPT1 Antibodies)-7)/Mas axis protected against pulmonary fibrosis by inhibiting the MAPK (show MAPK1 Antibodies)/NF-kappaB (show NFKB1 Antibodies) pathway.
A proximal promoter construct for the MAS gene was repressed by the SOX (show PIPOX Antibodies) [SRY (show SRY Antibodies) (sex-determining region on the Y chromosome) box] proteins SRY (show SRY Antibodies), SOX2 (show SOX2 Antibodies), SOX3 (show SOX3 Antibodies) and SOX14 (show SOX14 Antibodies), of which SRY (show SRY Antibodies) is known to interact with the KRAB domain.
Mas appears to be a critical component required for NO-mediated vasodilatation induced by renin angiotensin system-dependent and RAS-independent agonists and therefore arises as a key pharmacological target to modulate endothelial function
Control of adipogenesis by the autocrine interplays between angiotensin 1-7/Mas receptor and angiotensin II/AT1 receptor (show AGTRAP Antibodies) signaling pathways.
MasR was significantly upregulated in colon adenocarcinoma compared with non-neoplastic colon mucosa, which showed little or no expression of it. ACE (show ACE Antibodies) gene expression and enzymatic activity were also increased in the tumors.
Activation of Mas during myocardial infarction contributes to ischemia-reperfusion injury and suggest that inhibition of Mas-G(q) signaling may provide a new therapeutic strategy directed at cardioprotection.
MAS receptors mediate vasoprotective and atheroprotective effects of candesartan upon the recovery of vascular ACE2 (show ACE2 Antibodies)-angiotensin-(1-7)-MAS axis functionality
Mas receptor deficiency results in exacerbated inflammation in LPS (show TLR4 Antibodies)-challenged mice, which suggest a potential role for the Mas receptor as a regulator of systemic and brain inflammatory response induced by LPS (show TLR4 Antibodies).
a Mas receptor-mediated mechanism may stimulate pancreatic cell development
Hydronephrosis led to an increase of ACE (show ACE Antibodies) level and a decrease of ACE2 (show ACE2 Antibodies) and Mas receptor in the heart.
TGF-beta (show TGFB1 Antibodies) inhibits Mas receptor expression in fibroblasts but not in myoblasts or differentiated myotubes in animal model of muscular distrophy.
Deletion of the MasR causes marked increase in the aortic intima:media ratio, which is not due to generalized cellular proliferation.
The complete mouse Mas gene structure and organization.
Participation of AT1 (show SLC33A1 Antibodies) and Mas receptors in the modulation of inflammatory pain.
Klkb1 (show KLKB1 Antibodies)(-/-) mice have a novel mechanism for thrombosis protection in addition to reduced contact activation. This pathway arises when bradykinin delivery to vasculature is compromised and mediated by increased receptor Mas, prostacyclin, Sirt1 (show SIRT1 Antibodies), and KLF4 (show KLF4 Antibodies)
Ang-(1 (show ANGPT1 Antibodies)-7) counteracts the skeletal muscle atrophy induced by AngII through a mechanism dependent on the Mas receptor, which involves AKT (show AKT1 Antibodies) activity.
oncogene\; may be involved in function or development of neural tissues
, proto-oncogene Mas
, MAS proto-oncogene
, angiotensin-(1-7) receptor