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General TSC2 ELISA Kit for Competition ELISA - ABIN1140792
Feruglio, Trøseid, Damås, Kvale, Dyrhol-Riise: Soluble markers of the Toll-like receptor 4 pathway differentiate between active and latent tuberculosis and are associated with treatment responses. in PLoS ONE 2013
This is the first report using an animal model to show interactions between tsc2, mTORC1 and p53 (show TP53 ELISA Kits) during tumorigenesis.
These results demonstrate a highly conserved role of tsc2 in zebrafish and establish a new animal model for studies of Tuberous sclerosis complex.
Clinical whole exome sequencing of blood and tumor samples con (show DISP1 ELISA Kits) fi rmed the diagnosis of methylmalonic acidemia and revealed two somatic inactivating mutations in TSC2, suggesting the potential consideration of an mTOR (show FRAP1 ELISA Kits) inhibitor in the event of tumor recurrence.
TSC2 N-terminal lysine acetylation status affects to its stability modulating mTORC1 signaling and autophagy/cell proliferation.
The mTOR (show FRAP1 ELISA Kits)-dependent, epithelial phenotype of TSC (show SLC12A3 ELISA Kits) astrocytes suggests TSC1 (show TSC1 ELISA Kits)/2 and mTOR (show FRAP1 ELISA Kits) tune the phosphorylation level of catenin delta-1 (show CTNND1 ELISA Kits) by controlling PKCe (show PRKCE ELISA Kits) activity, thereby regulating the mesenchymal-epithelial-transition (MET)
TSC2 mutations leading to severe tuberous sclerosis in Chinese children.
Our results indicate that TSC2 and less commonly TSC1 (show TSC1 ELISA Kits) alterations are the primary essential driver event in angiomyolipoma/Lymphangioleiomyomatosis, whereas other somatic mutations are rare and likely do not contribute to tumor development.
These results suggested that TSC2 heterozygosity caused neurological malformations in primitive neural stem cells, indicating that its heterozygosity might be sufficient for the development of neurological abnormalities in patients.
brain somatic mutations in TSC1 (show TSC1 ELISA Kits) and TSC2 cause focal cortical dysplasia
the first structural information on TSC2/tuberin with novel insight into the molecular function.
Repression of TSC1 (show TSC1 ELISA Kits)/TSC2 mediated by MeCP2 (show MECP2 ELISA Kits) regulates human embryo lung fibroblast cell differentiation and proliferation.
Novel TSC2 mutations in Chinese patients with tuberous sclerosis.
this study shows that TSC2 maintains macrophage quiescence and prevents mTORC1-dependent granulomatous disease with clinical implications for sarcoidosis
Formation of ROS (show ROS1 ELISA Kits) and activity of NADPH (show FDXR ELISA Kits) oxidases were significantly higher in mouse embryonic fibroblasts and in primary culture of rat renal proximal tubular epithelial tuberin-deficient cells compared to wild-type cells.
Data suggest that pathological cardiac hypertrophy involved class I histone deacetylases HDAC1 (show HDAC1 ELISA Kits) and HdAC2 (show HDAC2 ELISA Kits), tuberous sclerosis complex 2 (TSC2), and mTOR (show FRAP1 ELISA Kits) srine-threonine kinases (mTOR (show FRAP1 ELISA Kits)).
autophagy via the TSC2-mTORC1 signaling pathway plays an important role in maintenance of cardiac function and mitochondrial quantity and size in the heart.
PAK2 (show PAK2 ELISA Kits) is a direct effector of TSC1 (show TSC1 ELISA Kits)-TSC2-RHEB (show RHEB ELISA Kits) signaling and a new target for rational drug therapy in TSC (show SLC12A3 ELISA Kits).
Data indicate that an AMP (show TMPRSS5 ELISA Kits)-ctivated kinase (AMPK (show PRKAA1 ELISA Kits))/cell-cycle inhibitor p27KIP1 (p27 (show CDKN1B ELISA Kits)) axis drives activation of autophagy in rapamycin-treated tuberous sclerosis 2 protein (Tsc2)-null cells.
Lysosomal recruitment of TSC2 is a universal response to stimuli that inactivate mTORC1, and that the presence of any single stress is sufficient to cause TSC2 lysosomal localization.
Axitinib is an effective inhibitor of Tsc2-null lesion growth.
Porcine circovirus type 2 (PCV2) might induce autophagy via the AMPK (show PRKAA1 ELISA Kits)/ERK (show MAPK1 ELISA Kits)/TSC2/mTOR (show FRAP1 ELISA Kits) signaling pathway in the host cells, representing a pivotal mechanism for PCV2 pathogenesis
prostaglandin F2alpha phosphorylates TSC2 and activates mTOR (show FRAP1 ELISA Kits) and ribosomal protein S6 (show RPS6 ELISA Kits) kinase (show RPS6KB1 ELISA Kits) signaling in an AKT (show AKT1 ELISA Kits)-independent manner
Mutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms.
tuberous sclerosis complex 2 (TSC2)
, tuberous sclerosis 2
, tuberous sclerosis 2 protein
, tuberous sclerosis 2 protein homolog
, renal carcinoma
, tuberous sclerosis 2 homolog protein