12 Results for: "TLC EXPLORER"
Accessories for Supelco® TLC Explorer Documentation System, MilliporeSigma
Supplier: MilliporeSigma
Accessories for Supelco® TLC Explorer Documentation System, MilliporeSigma
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Supelco® TLC Explorer Documentation System, MilliporeSigma
Supplier: MilliporeSigma
Superior instrumental solution for reliable TLC plate analysis. It can analyze one or multiple plates up to an area of 20×20 cm. In addition, the device uses three LED light sources – white light (VIS), UV-A (366 nm), and UV-C (254 nm) to illuminate the plates from above in direct-light mode. It allows a quick visual check or a software-based analysis and quantification.
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Amino Acid Analysis by TLC Lab Activity.
Supplier: Kemtec
Explore the Theory of Chromatography.
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STAT3 Inhibitor V, Stattic ≥98% (by TLC)
Supplier: Enzo Life Sciences
Small molecule STAT3-specific inhibitor which blocks activation, dimerization and nuclear translocation via binding to the STAT3 SH2 domain. It is a very useful tool for exploring STAT3-mediated signaling pathways. It blocks LPS-mediated STAT3 tyrosine phosphorylation which leads to inhibition of LPS-mediated IL-1β and IL-6 production. In primary cultures of rat neural stem cells it blocks IL-15-induced differentiation.
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IAXO-101 (CD14/TLR4 Antagonist) (synthetic) ≥98% (by TLC)
Supplier: Adipogen
CD14/TLR4 antagonist. Inhibitor of sterile inflammation. Synthetic TLR4/CD14 ligand with TLR4 modulating activities in vitro, and conferring protection against TLR4/CD14-mediated tissue damage and inflammation in vivo. Useful to explore CD14- dependent and TLR4-independent pathways and TLR4 activation by endogenous ligands (e.g. hyaluronic acid oligosaccharides, oxLDL, HMGB1) in sterile inflammation. Shown to inhibit neuropathic pain, secondary necrosis of acute drug-induced liver failure and vascular inflammation, and abdominal aortic aneurysm by blocking non-hematopoietic TLR4 signaling. Useful tool, where inhibition of sterile (auto-) inflammation is desired, without compromising TLR4’s key role in the defense of pathogens.
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IAXO-103 (CD14/TLR4 Antagonist) (synthetic) ≥98% (by TLC)
Supplier: Adipogen
CD14/TLR4 antagonist. Inhibitor of sterile inflammation. Synthetic TLR4/CD14 ligand with TLR4 modulating activities in vitro, and conferring protection against TLR4/CD14-mediated tissue damage and inflammation in vivo. Useful to explore CD14- dependent and TLR4-independent pathways and TLR4 activation by endogenous ligands (e.g. hyaluronic acid oligosaccharides, oxLDL, HMGB1) in sterile inflammation. Shown to inhibit neuropathic pain, secondary necrosis of acute drug-induced liver failure and vascular inflammation, and abdominal aortic aneurysm by blocking non-hematopoietic TLR4 signaling. Useful tool, where inhibition of sterile (auto-) inflammation is desired, without compromising TLR4’s key role in the defense of pathogens.
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IAXO-102 (CD14/TLR4 Antagonist) (synthetic) ≥98% (by TLC)
Supplier: Adipogen
CD14/TLR4 antagonist. Inhibitor of sterile inflammation. Synthetic TLR4/CD14 ligand with TLR4 modulating activities in vitro, and conferring protection against TLR4/CD14-mediated tissue damage and inflammation in vivo. Useful to explore CD14- dependent and TLR4-independent pathways and TLR4 activation by endogenous ligands (e.g. hyaluronic acid oligosaccharides, oxLDL, HMGB1) in sterile inflammation. Shown to inhibit neuropathic pain, secondary necrosis of acute drug-induced liver failure and vascular inflammation, and abdominal aortic aneurysm by blocking non-hematopoietic TLR4 signaling. Useful tool, where inhibition of sterile (auto-) inflammation is desired, without compromising TLR4’s key role in the defense of pathogens.
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7-Oxo-7H-benzo[de]benzo[4,5]imidazo[2,1-a]isoquinoline-3-carboxylic acid ≥98% (by TLC)
Supplier: Enzo Life Sciences
CaM kinase kinase inhibitor
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GW 9508 ≥98% (by TLC)
Supplier: Enzo Life Sciences
High potency synthetic agonist at GPR40.
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ZK-756326 ≥98% (by TLC), white solid
Supplier: Enzo Life Sciences
CCR8 activator.
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17-AAG
Supplier: RPI
17-AAG (17-Allylamino-17-demethoxygeldanamycin) is a synthetic derivative of geldanamycin. Like geldanamycin, 17-AAG is recognised for its role as an inhibitor of heat shock protein 90 (Hsp90), a molecular chaperone involved in protein folding and stabilisation.