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LY 294002 1PC X 5MG
Кат. №: 440202-10MG
Производитель: Sigma-Aldrich
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LY 294002 1PC X 5MG
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Кат. №: 440202-10MG
Производитель: Sigma-Aldrich
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Цена по запросу
Товар оформляется под заказ
Main image
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LY 294002 1PC X 5MG
Кат. №: 440202-10MG
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Description General description A cell-permeable, potent, reversible and specific phosphatidylinositol 3-kinase inhibitor (IC50 = 1.4 µM) that acts on the ATP-binding site of the enzyme. Also inhibits nonhomologous DNA end-joining (NHEJ) activity of the 460 kDa phosphatidylinositol 3-like kinase DNA-PKcs, which is the catalytic subunit of DNA-activated protein kinase. Does not affect the activities of EGF receptor kinase, MAP kinase, PKC, Pl 4-kinase, S6 kinase, and c-Src even at 50 µM. Promotes the nuclear accumulation of active GSK-3b. Reported to suppress the proliferation of murine embryonic stem cells. Blocks the proliferation of cultured rabbit aortic smooth muscle cells without inducing apoptosis. Shown to bind to the same site as I-BET (Cat. No. 40101050 ~ 10 µM). A 10 mM (1 mg/325 µl) solution of LY 294002 (Cat. No. 440204) in DMSO is also available. A cell-permeable, potent, reversible, and specific phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor that acts on the ATP-binding site of the enzyme (IC50 = 1.4 µM). Also inhibits nonhomologous DNA end-joining (NHED) in the 460 kDa phosphatidylinositol 3-like kinase DNA-PKcs, which is the catalytic subunit of DNA-activated protein kinase. Does not affect the activity of EGF receptor kinase, MAP kinase, PKC, PI 4-kinase, S6 kinase, and c-src at 50 µM. Promotes the nuclear accumulation of active GSK-3b. Reported to suppress the proliferation of murine embryonic stem cells. Blocks the proliferation of cultured rabbit aortic smooth muscle cells without inducing apoptosis. Reported to inhibit histamine secretion in RBL-2H3 cells (IC50 = 5 µM). Packaging 5, 10, 25 mg in Plastic ampoule Biochem/physiol Actions Cell permeable: yes Primary Target Phosphatidylinositol 3-kinase Product competes with ATP. Reversible: yes Target IC50: 1.4 µM against phosphatidylinositol 3-kinase Warning Toxicity: Standard Handling (A) Preparation Note Slight warming may be required to achieve complete solubilization. Reconstitution Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. Other Notes Dittman, A., et al. 2013. ACS Chem. Biol.9, 495. Bechard, M., and Dalton. S. 2009. Mol. Cell. Biol.29, 2092. Lianguzova, M.S. et al. 2007. Cell Biol. Int.31, 330. Baumann, P., and West, S.C. 1998. Proc. Natl. Acad. Sci. USA 95, 14066. Cardone, M.H., et al. 1998. Science282, 1318. Vlahos, C.J., et al. 1995. J. Immunol.154, 2413. Yano, H., et al. 1995. Biochem. J.312, 145. Vlahos, C.J., et al. 1994. J. Biol. Chem.269, 5241. Selected Citations Lee, J., et al. 2009. Cell Stem Cell5, 76.
Related Categories
Cell Biology, Cell Signaling and Neuroscience, Kinase/Phosphatase Biology, Protein Kinase Inhibitors Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description General description A cell-permeable, potent, reversible and specific phosphatidylinositol 3-kinase inhibitor (IC50 = 1.4 µM) that acts on the ATP-binding site of the enzyme. Also inhibits nonhomologous DNA end-joining (NHEJ) activity of the 460 kDa phosphatidylinositol 3-like kinase DNA-PKcs, which is the catalytic subunit of DNA-activated protein kinase. Does not affect the activities of EGF receptor kinase, MAP kinase, PKC, Pl 4-kinase, S6 kinase, and c-Src even at 50 µM. Promotes the nuclear accumulation of active GSK-3b. Reported to suppress the proliferation of murine embryonic stem cells. Blocks the proliferation of cultured rabbit aortic smooth muscle cells without inducing apoptosis. Shown to bind to the same site as I-BET (Cat. No. 40101050 ~ 10 µM). A 10 mM (1 mg/325 µl) solution of LY 294002 (Cat. No. 440204) in DMSO is also available. A cell-permeable, potent, reversible, and specific phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor that acts on the ATP-binding site of the enzyme (IC50 = 1.4 µM). Also inhibits nonhomologous DNA end-joining (NHED) in the 460 kDa phosphatidylinositol 3-like kinase DNA-PKcs, which is the catalytic subunit of DNA-activated protein kinase. Does not affect the activity of EGF receptor kinase, MAP kinase, PKC, PI 4-kinase, S6 kinase, and c-src at 50 µM. Promotes the nuclear accumulation of active GSK-3b. Reported to suppress the proliferation of murine embryonic stem cells. Blocks the proliferation of cultured rabbit aortic smooth muscle cells without inducing apoptosis. Reported to inhibit histamine secretion in RBL-2H3 cells (IC50 = 5 µM). Packaging 5, 10, 25 mg in Plastic ampoule Biochem/physiol Actions Cell permeable: yes Primary Target Phosphatidylinositol 3-kinase Product competes with ATP. Reversible: yes Target IC50: 1.4 µM against phosphatidylinositol 3-kinase Warning Toxicity: Standard Handling (A) Preparation Note Slight warming may be required to achieve complete solubilization. Reconstitution Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. Other Notes Dittman, A., et al. 2013. ACS Chem. Biol.9, 495. Bechard, M., and Dalton. S. 2009. Mol. Cell. Biol.29, 2092. Lianguzova, M.S. et al. 2007. Cell Biol. Int.31, 330. Baumann, P., and West, S.C. 1998. Proc. Natl. Acad. Sci. USA 95, 14066. Cardone, M.H., et al. 1998. Science282, 1318. Vlahos, C.J., et al. 1995. J. Immunol.154, 2413. Yano, H., et al. 1995. Biochem. J.312, 145. Vlahos, C.J., et al. 1994. J. Biol. Chem.269, 5241. Selected Citations Lee, J., et al. 2009. Cell Stem Cell5, 76.
Related Categories
Cell Biology, Cell Signaling and Neuroscience, Kinase/Phosphatase Biology, Protein Kinase Inhibitors Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.

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