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EMILIN1 encodes an extracellular matrix glycoprotein that is characterized by an N-terminal microfibril interface domain, a coiled-coiled alpha-helical domain, a collagenous domain and a C-terminal globular C1q domain. De plus, nous expédions Emilin1 Anticorps (47) et Emilin1 Protéines (9) et beaucoup plus de produits pour cette protéine.
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Expression of certain emilin genes in peculiar areas, such as the central nervous system or the posterior notochord, suggests that they may play a role in key morphogenetic processes:[Emilin]
Data suggested mechanisms for homo- and hetero-typic EMILINs multimers formation: EMILIN1 or EMILIN2 (Montrer EMILIN2 Kits ELISA) alone can form trimers and multimers in the absence of each other or they can co-polymerize in a head-to-tail fashion to form hetero-typic multimers.
Emilin1 deficiency results in aortic valve disease, mediated by non-canonical (MAPK (Montrer MAPK1 Kits ELISA)/phosphorylated Erk1 (Montrer MAPK3 Kits ELISA) and Erk2 (Montrer MAPK1 Kits ELISA)) TGF-beta (Montrer TGFB1 Kits ELISA) dysregulation.
EMILIN1/integrin alpha 9 beta 1 interaction contributes to lymphatic valve formation, maintenance, and function.
these data established that EMILIN1 exerts a protective role in tumor growth, in tumor lymphatic vessel formation, as well as in metastatic spread to lymph nodes
Emilin-1 produced by vascular smooth muscle cells acts as a main regulator of resting blood pressure levels by controlling the myogenic response in resistance arteries through TGF-beta (Montrer TGFB1 Kits ELISA).
Pull-down assays indicated that the binding to organ of Corti CNGA3 was attributable to the EMILIN1 intracellular sequence that follows a predicted transmembrane domain in the C-terminus
EMILIN1 is identified as a novel ligand for keratinocyte alpha9beta1 integrin, suggesting prospective roles for this receptor-ligand pair in skin homeostasis.
EMILIN1 is a novel local regulator of lymphangiogenesis
This study is the first to identify EMILIN-1 and ILK (Montrer ILK Kits ELISA) as prospective markers of islet regenerative function in human mesenchymal stem cells.
These findings collectively suggest that EMILIN1 may represent a new disease gene associated with an autosomal-dominant connective tissue disorder.
The present findings highlight the peculiar activity of PMN elastase (Montrer ELANE Kits ELISA) in disabling EMILIN1 suppressor function.
All three SNPs in introns 1 and 5 (rs2289360, rs2011616 and rs7424556) of EMILIN1 were in strong pair-wise linkage disequilibrium and were significantly associated with hypertension.
There were significant associations of rs2011616 and rs2304682 polymorphisms in the EMILIN1 gene with hypertension among Japanese.
EMILIN-1 may regulate the formation of oxytalan fibers and play a role in their homeostasis.
rs2289360, rs2011616, and rs2304682 in the human EMILIN1 gene, as well as the haplotype constructed using rs2536512, rs2011616, and rs17881426, are useful genetic markers of essential hypertension in Japanese men.
NMR assignments for the C-terminal globular domain of EMILIN-1
This gene encodes an extracellular matrix glycoprotein that is characterized by an N-terminal microfibril interface domain, a coiled-coiled alpha-helical domain, a collagenous domain and a C-terminal globular C1q domain. The encoded protein associates with elastic fibers at the interface between elastin and microfibrils and may play a role in the development of elastic tissues including large blood vessels, dermis, heart and lung.
, elastin microfibril interfacer 1
, elastin microfibril interface located protein 1
, elastin microfibril interface-located protein 1
, elastin microfibril interface located protein