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12 results for "TLC EXPLORER"

12 Results for: "TLC EXPLORER"

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Accessories for Supelco® TLC Explorer Documentation System, MilliporeSigma

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

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.

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)

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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ZM-323881 ≥98% (by TLC)

Supplier: Enzo Life Sciences

VEGFR 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

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.

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