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anti-Human Angiomotin Antikörper:
anti-Mouse (Murine) Angiomotin Antikörper:
anti-Rat (Rattus) Angiomotin Antikörper:
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Human Polyclonal Angiomotin Primary Antibody für DB - ABIN1881054
Heller, Adu-Gyamfi, Smith-Kinnaman, Babbey, Vora, Xue, Bittman, Stahelin, Wells: Amot recognizes a juxtanuclear endocytic recycling compartment via a novel lipid binding domain. in The Journal of biological chemistry 2010
Show all 5 Pubmed References
Human Polyclonal Angiomotin Primary Antibody für WB - ABIN531071
Chan, Lim, Chong, Pobbati, Huang, Hong: Hippo pathway-independent restriction of TAZ and YAP by angiomotin. in The Journal of biological chemistry 2011
Show all 2 Pubmed References
Human Polyclonal Angiomotin Primary Antibody für IF (p), IHC (p) - ABIN754873
Shimada, Abe, Kohno, Satohisa, Konno, Takahashi, Hatakeyama, Arimoto, Kakuki, Kaneko, Takano, Saito, Kojima: Loss of tricellular tight junction protein LSR promotes cell invasion and migration via upregulation of TEAD1/AREG in human endometrial cancer. in Scientific reports 2017
Data indicate that Amot is crucial for the maintenance of nuclear YAP (zeige YAP1 Antikörper) to promote renal epithelial and RCC (zeige XRCC1 Antikörper) proliferation.
Decreased AMOT-p130 (zeige RBL2 Antikörper) expression coupled with high nuclear YAP1 (zeige YAP1 Antikörper) 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 (zeige RAB1A Antikörper) in the progression of colon cancer by activating the YAP (zeige YAP1 Antikörper)-ERK (zeige EPHB2 Antikörper)/PI3K (zeige PIK3CA Antikörper)-AKT (zeige AKT1 Antikörper) 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 (zeige MLXIP Antikörper)-205 significantly downregulated and directly target the 3'-UTR (zeige UTS2R Antikörper) of AMOT in breast cancer. In vitro, miR (zeige MLXIP Antikörper)-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 (zeige YAP1 Antikörper), YAP (zeige YAP1 Antikörper)/TAZ (zeige TAZ Antikörper) and LATS1 (zeige LATS1 Antikörper).
experiments indicate that AMOT and other motin family members function together with NEDD4L (zeige NEDD4L Antikörper) 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 (zeige YAP1 Antikörper) stimulator in high glucose level.
Rho attenuates the interaction between Amot and Nf2 (zeige NF2 Antikörper) by binding to the coiled-coil domain of Amot.
TFPI-1 (zeige TFPI Antikörper) interacts with AMOT, which led to a decrease in the phosphorylation of YAP (zeige YAP1 Antikörper) 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 (zeige RNF146 Antikörper) 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 (zeige YAP1 Antikörper) and Teads (TEA domain family members) and contributed to the regulation of a subset of Yap (zeige YAP1 Antikörper) target genes, many of which are associated with tumorigenesis.
The loss of Angiomotin, together with Angiomotin-like 2 (zeige AMOTL2 Antikörper), leads to differentiation of inner cell mass cells and compromised peri (zeige POSTN Antikörper)-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 (zeige AMOTL1 Antikörper), and Amotl2 (zeige AMOTL2 Antikörper) are differentially expressed in uterine cells during the peri (zeige POSTN Antikörper)-implantation period.
A vaccine targeting angiomotin induces an antibody response which alters tumor vessel permeability and hampers the growth of established tumors.
Thus AMOT is a direct substrate of Lats1 (zeige LATS1 Antikörper)/2 mediating functions of the Hippo pathway in endothelial cell migration and angiogenesis.
knockdown of Amot reduced the number of filopodia of endothelial tip cells and severely impaired the migration of intersegmental vessels
Amot and AmotL1 (zeige AMOTL2 Antikörper) have similar effects on endothelial migration and tight junction formation in vitro. In vivo Amot appears to control the cell polarity and AmotL1 (zeige AMOTL2 Antikörper) affects the stability of cell-cell junctions.
Amot and AmotL1 (zeige AMOTL1 Antikörper) have similar effects on endothelial migration and tight junction formation in vitro. In vivo Amot appears to control the cell polarity and AmotL1 (zeige AMOTL1 Antikörper) affects the stability of cell-cell junctions.
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