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Amot and AmotL1 have similar effects on endothelial migration and tight junction formation in vitro. In vivo Amot appears to control the cell polarity and AmotL1 affects the stability of cell-cell junctions.
Thus AMOT is a direct substrate of Lats1/2 mediating functions of the Hippo pathway in endothelial cell migration and angiogenesis.
knockdown of Amot reduced the number of filopodia of endoth (show PDPN Proteins)elial tip cells and severely impaired the migration of intersegmental vessels
Data indicate that Amot is crucial for the maintenance of nuclear YAP (show YAP1 Proteins) to promote renal epithelial and RCC (show XRCC1 Proteins) proliferation.
Decreased AMOT-p130 (show RBL2 Proteins) expression coupled with high nuclear YAP1 (show YAP1 Proteins) expression resulted in shorter overall survival and disease-free survival in patients with advanced gastric cancer.
Study focused on the methylation profile of the AMOT promoter CpG island during development, comparing it in circulating cord blood endothelial progenitor cells (ECFC) of cord blood from term versus preterm newborns. Findings highlight importance of pro-angiogenic AMOT gene methylation in ECFC, suggesting that epigenetic mechanisms may control the regulation of angiogenesis during development.
AMOT may function as an oncogene (show RAB1A Proteins) in the progression of colon cancer by activating the YAP (show YAP1 Proteins)-ERK (show EPHB2 Proteins)/PI3K (show PIK3CA Proteins)-AKT (show AKT1 Proteins) signaling pathway.
The lncRNA SNHG12 promotes cell proliferation and migration by upregulating AMOT gene expression in osteosarcoma cells in vivo and in vitro.
angiomotin and Merlin respectively interface cortical actin filaments and core kinases in Hippo signaling
Study shows miR (show MLXIP Proteins)-205 significantly downregulated and directly target the 3'-UTR of AMOT in breast cancer. In vitro, miR (show MLXIP Proteins)-205 regulates the proliferation and invasion of breast cancer cells through suppression of AMOT expression.
Amot was highly expressed in breast cancer tissues and was important in the promotion of breast cancer cell proliferation and invasion. Amot knockdown in MCF-7 cells decreased the expression of YAP, YAP/TAZ and LATS1.
experiments indicate that AMOT and other motin family members function together with NEDD4L (show NEDD4L Proteins) to help complete immature virion assembly prior to ESCRT-mediated virus budding
AMOT is a crucial suppressor of lung cancer metastasis and highlight its critical role as a tumor suppressor and its potential as a prognostic biomarker and therapeutic target for lung cancer.
Collectively, we have uncovered that AMOT acts as a YAP (show YAP1 Proteins) stimulator in high glucose level.
Rho attenuates the interaction between Amot and Nf2 (show NF2 Proteins) by binding to the coiled-coil domain of Amot.
TFPI-1 (show TFPI Proteins) interacts with AMOT, which led to a decrease in the phosphorylation of YAP (show YAP1 Proteins) and further increased the genes expression of the proliferation and migration involved. Our results further confirmed that atherosclerosis was a localized disease.
a new function of RNF146 (show RNF146 Proteins) and tankyrase in stabilizing the Crumbs complex through downregulation of AMOT proteins at the apical membrane, is reported.
Within the nucleus, Amot-p130 was associated with the transcriptional complex containing Yap (show YAP1 Proteins) and Teads (TEA domain family members) and contributed to the regulation of a subset of Yap (show YAP1 Proteins) target genes, many of which are associated with tumorigenesis.
The loss of Angiomotin, together with Angiomotin-like 2 (show AMOTL2 Proteins), leads to differentiation of inner cell mass cells and compromised peri (show POSTN Proteins)-implantation development.
The phosphorylation of S176 in the N-terminal domain of Amot is a critical step for activation of the Hippo pathway in adherens junctions and cell polarity disconnects the Hippo pathway from cell-cell adhesion by sequestering Amot from AJs.
Amot, Amotl1, and Amotl2 (show AMOTL2 Proteins) are differentially expressed in uterine cells during the peri (show POSTN Proteins)-implantation period.
A vaccine targeting angiomotin induces an antibody response which alters tumor vessel permeability and hampers the growth of established tumors.
This gene belongs to the motin family of angiostatin binding proteins characterized by conserved coiled-coil domains and C-terminal PDZ binding motifs. The encoded protein is expressed predominantly in endothelial cells of capillaries as well as larger vessels of the placenta where it may mediate the inhibitory effect of angiostatin on tube formation and the migration of endothelial cells toward growth factors during the formation of new blood vessels. Alternative splicing results in multiple transcript variants encoding different isoforms.
angiomotin p130 isoform
, angiomotin p80 isoform