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EnteroPluri-Test is a 12-sector system containing special culture media for the identification of Enterobacteriaceae and other Gram-negative, oxidase negative bacteria.
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A JAK1 inhibitor (IC50 47 nM) selective for JAK1 over JAK3 and Tyk2 (IC50s 2304 and 4690 nM respectively) as well as a panel of 83 additional kinases at 1 UM but does inhibit JAK2 ROCK1 and ROCK2 (IC50s 120 920 and 430 nM respectively) decreases cytokine-induced STAT phosphorylation in a variety of human cells (IC50s 1.6-649 nM) reduces M. tuberculosis-induced paw swelling and bone erosion in a rat model of arthritis at 1 3 and 10 mg/kg twice per day for 17 days
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A typical antipsychotic inhibits spontaneous motor activity and responding for food in rats as well as potentiates hexobarbital-induced narcosis in mice inhibits lysosome acidification as well as viral entry (IC50 8.5 UM) in Ebola-infected Huh7 cells
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This product is for research use only and not for diagnostic or therapeutic procedures. Customer is granted a limited, non-exclusive license for internal research and shall not attempt to reverse engineer. Triciribine, inhibitor of Akt activation.
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Chemical. CAS 750590-18-2. Formula C8H4O3S2. MW 212.3. Isolated from Roseobacter gallaeciensis. Antibiotic. Isomeric to thiotropocin. Antibacterial. Active against Gram-positive and Gram-negative bacteria. Antifungal and anti-nematodical. Shows antitumor activity. Cytotoxic against selected mammalian neuronal cell lines. Bacterial signal substance.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Chemical. CAS 750590-18-2. Formula C8H4O3S2. MW 212.3. Isolated from Roseobacter gallaeciensis. Antibiotic. Isomeric to thiotropocin. Antibacterial. Active against Gram-positive and Gram-negative bacteria. Antifungal and anti-nematodical. Shows antitumor activity. Cytotoxic against selected mammalian neuronal cell lines. Bacterial signal substance.
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. PIN1 inhibitor API-1 is a specific Pin1 inhibitor (IC50 72.3 nM). PIN1 inhibitor API-1 retains the active conformation of pXPO5 and restores the ability of pXPO5 to transport pre-miRNAs from the nucleus to cytoplasm thus up-regulating the anticancer miRNA biogenesis to suppress both in vitro and in vivo hepatocellular carcinoma development. PIN1 inhibitor API-1 directly and specifically binds to the Pin1 peptidyl-prolyl isomerase domain and effectively inhibits Pin1 cis-trans isomerizing activity. purity: 98%
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