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The protein encoded by TAGLN is a transformation and shape-change sensitive actin cross-linking/gelling protein found in fibroblasts and smooth muscle. Zusätzlich bieten wir Ihnen Transgelin Kits (22) und Transgelin Proteine (15) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 181 products:
Human Polyclonal Transgelin Primary Antibody für ELISA, WB - ABIN153392
Nishida, Kitami, Abe, Hiwada: Gene cloning and nucleotide sequence of SM22 alpha from the chicken gizzard smooth muscle. in Biochemistry international 1991
Show all 19 Pubmed References
Human Polyclonal Transgelin Primary Antibody für ELISA, WB - ABIN185188
Donati, Marseglia, Magi, Serratì, Cencetti, Bernacchioni, Nannetti, Benelli, Brunelli, Torricelli, Cossu, Bruni: Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. in PLoS ONE 2011
Show all 5 Pubmed References
Human Polyclonal Transgelin Primary Antibody für ICC, IF - ABIN442948
Shi, Srivastava, Kanasaki, He, Kitada, Nagai, Nitta, Takagi, Kanasaki, Koya: Interactions of DPP-4 and integrin β1 influences endothelial-to-mesenchymal transition. in Kidney international 2015
Show all 2 Pubmed References
Human Monoclonal Transgelin Primary Antibody für IF, ELISA - ABIN948519
Canducci, Saita, Foglieni, Piscopiello, Chiesa, Colombo, Cianflone, Maseri, Clementi, Burioni: Cross-reacting antibacterial auto-antibodies are produced within coronary atherosclerotic plaques of acute coronary syndrome patients. in PLoS ONE 2012
Human Polyclonal Transgelin Primary Antibody für ICC, IF - ABIN4362001
Isella, Terrasi, Bellomo, Petti, Galatola, Muratore, Mellano, Senetta, Cassenti, Sonetto, Inghirami, Trusolino, Fekete, De Ridder, Cassoni, Storme, Bertotti, Medico: Stromal contribution to the colorectal cancer transcriptome. in Nature genetics 2015
High expression level of TAGLN is associated with prostate cancer.
this study identified potential biochemical players involved in distant recurrence and indicates that R-Ras and Transgelin are potential post-surgical prognostic biomarkers for Stage III colorectal cancer
During transition from the pluripotent stage towards the neural developmental stage, TAGLN is differentially expressed in bipolar patient derived cells compared to control derived cells.
Data (including data from studies using cells cultured from transgenic/knockout mice) suggest that expression and degradation of transgelin in myofibroblasts and keratinocytes are regulated by mechanical tension in cytoskeleton produced by myosin II motor in response to stiffness of culture matrix/extracellular matrix.
transgelin (TAGLN), a transforming growth factor beta (TGFbeta (zeige TGFB1 Antikörper))-inducible gene, was identified as an upregulated gene during in vitro osteoblastic and adipocytic differentiation of human bone marrow-derived stromal (skeletal) stem cells
regulates vasculogenic mimicry in breast cancer cells by enhancing interleukin-8 (zeige IL8 Antikörper) uptake
Serum concentrations of CK-18 (zeige KRT18 Antikörper) fragments and transgelin-2 (zeige TAGLN2 Antikörper) correlate with the severity of NAFLD (zeige TSC2 Antikörper), but not with obesity.
Increases or decreases in transgelin levels have reciprocal effects on tumor cell behavior, with higher expression promoting metastasis
activated AKT (zeige AKT1 Antikörper) and JNK (zeige MAPK8 Antikörper) signaling pathways promote the overexpression of transgelin
Cofilin-1 (zeige CFL1 Antikörper) and transgelin may play roles in the carcinogenesis and development of esophageal squamous cell carcinoma
findings reveal for the first time that SM22 is expressed in the nucleus in addition to the cytoplasm of VSMCs to regulate the transcription of Nik and its downstream proinflammatory NF-kB signal pathways as a modulator of SRF during vascular inflammation
The disruption of SM22alpha enhances PDGF-BB-induced GLUT4 translocation and glucose uptake by promoting actin dynamics and cortical actin polymeriza- tion.
Targeted elimination of TGFbetaR2 in TAGLN(+) cells impairs midline closure and prevents the correct subsequent patterning of the musculature and skeletal components.
SM22alpha is a phosphorylation-regulated (zeige PHAX Antikörper) suppressor of IKK (zeige CHUK Antikörper)-IkappaBalpha (zeige NFKBIA Antikörper)-NF-kappaB (zeige NFKB1 Antikörper) signaling cascades.
SM22alpha promotes ubiquitination and degradation of MKP3 (zeige DUSP6 Antikörper). SM22alpha facilitates AngII-induced contraction by maintenance of ERK1/2 (zeige MAPK1/3 Antikörper) signaling.
TRAF6 (zeige TRAF6 Antikörper)-SM22alpha-G6PD (zeige G6PD Antikörper) pathway is a novel mechanism underlying the association between glucose metabolism and VSMC survival, which is beneficial for vascular repair after injury but facilitates atherosclerotic plaque stability.
Absent/lower SM22 alpha levels favor an increase in parietal epithelial cell transition cells and PECs expressing a progenitor marker, and a lower epithelial mesenchymal transformation rate versus SM22alpha+/+mice, where SM22 levels are increased in PECs.
SM22alpha-regulated molecular pathways contribute to vascular pathology.
Histological analysis did not reveal calcium deposits in the aortic roots of SM22alpha-Rankl (zeige TNFSF11 Antikörper) ( tg ) mice
The protein encoded by this gene is a transformation and shape-change sensitive actin cross-linking/gelling protein found in fibroblasts and smooth muscle. Its expression is down-regulated in many cell lines, and this down-regulation may be an early and sensitive marker for the onset of transformation. A functional role of this protein is unclear. Two transcript variants encoding the same protein have been found for this gene.
, putative transgelin
, 22 kDa actin-binding protein
, smooth muscle protein 22-alpha
, transgelin variant 2
, actin-associated protein p27
, smooth muscle 22 protein
, 25 kDa F-actin-binding protein