48193 Results for: "Weighing+Papers&pageNo=8"

Fluoroquinolone antibacterial agent. Inhibits bacterial DNA gyrase (topoisomerase). Inhibits cell division and causes double-strand breaks in the bacterial chromosome. Broad-spectrum antibiotic effective against Gram-positive, Gram-negative and anaerobic bacteria.

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2-Bromo-2-butene cis- and trans-mixture ≥98% stabilised

Supplier: Thermo Fisher Scientific

Stabilized

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4-(Dimethylamino)cinnamaldehyde ≥98%

Supplier: Thermo Fisher Scientific

4-(Dimethylamino)cinnamaldehyde ≥98%

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3-Indolylglyoxalyl chloride ≥98%

Supplier: Thermo Fisher Scientific

3-Indolylglyoxalyl chloride ≥98%

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Dihydroergocristine methanesulphonate ≥98%, white solid

Supplier: ENZO LIFE SCIENCES

Serotonin receptor ligand.

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Ethyl-5,6-dimethoxyindole-2-carboxylate ≥98%

Supplier: Thermo Fisher Scientific

Ethyl-5,6-dimethoxyindole-2-carboxylate ≥98%

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(2'Z,3'E)-6-Bromoindirubin-3'-oxime ≥98%

Supplier: ENZO LIFE SCIENCES

Inibitor of phosphoinositide-dependent kinase 1 and GSK

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Butein ≥98% (by HPLC)

Supplier: ENZO LIFE SCIENCES

Tyrosine kinase inhibitor

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Rosmarinic acid ≥98% (by HPLC)

Supplier: ENZO LIFE SCIENCES

Rosmarinic acid ≥98% (by HPLC)

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1-Diethylamino-2-butyne, 98+% 1 * 1 g

Supplier: Thermo Fisher Scientific

1-Diethylamino-2-butyne, 98+% 1 * 1 g

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3,4-Di(1H-indol-3-yl)-1H-pyrrole-2,5-dione ≥98%

Supplier: ENZO LIFE SCIENCES

PKC inhibitor

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Bleomycin sulphate (mixture) ≥98% (by HPLC)

Supplier: ENZO LIFE SCIENCES

Anti-tumor agent. Induces apoptosis via DNA damage. Radiomimetic DNA-cleaving agent that produces double and single DNA strand breaks through an oxygen-radical-dependent mechanism. Inhibits intracellular DNA replication. DNA alkylating agent.

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Nocodazole ≥98%

Supplier: ENZO LIFE SCIENCES

Microtubule inhibitor

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Anti-IDO1 Rat Monoclonal Antibody [clone: mIDO-48]

Supplier: ENZO LIFE SCIENCES

Indoleamine 2,3-dioxygenase (IDO) is an IFN-γ inducible gene. It catalyzes the degradation of the essential amino acid L-tryptophan to N-formylkynurenine. IDO has been implicated in protection against intracellular and extracellular pathogens. The mIDO-48 monoclonal antibody recognizes mouse IDO also known as Indolamine 2,3-dioxygenase, Indole 2,3-dioxygenase, and Indoleamine-pyrrole 2,3-dioxygenase. This antibody does not appear to react with human IDO. IDO is a ubiquitously expressed cytoplasm protein with a predicted molecular weight approximately 45 kDa. Indoleamine 2,3-dioxygenase (IDO) is one the best known IFN-γ inducible genes. The product of IDO gene catalyzes the degradation of the essential amino acid L-tryptophan to N-formylkynurenine. IDO has been implicated in protection against intracellular and extracellular pathogens. It also has been shown to maintain the special immune suppressive status of immune-privileged sites such as the brain, eyes, kidney, and placenta. The IDO antibody has been shown to be useful for western blotting and Immunohistochemistry.

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Sodium phenoxide ≥98%

Supplier: Thermo Fisher Scientific

Sodium phenoxide ≥98%

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Midostaurin ≥98% (by TLC)

Supplier: ENZO LIFE SCIENCES

Inhibitor of a variety of serine/threonine and tyrosine kinases, like protein kinase C (PKC), cyclic AMP-dependent protein kinase (PKA), S6 kinase, Akt (protein kinase B; PKB), epidermal growth factor receptor (EGFR) tyrosine kinase activity and others including KDR, VEGFR, PDGFR, c-kit and other receptor tyrosine kinases. Potently inhibits FLT-3 kinase including mutant forms found in acute myeloid leukemia in vitro and in vivo. Apoptosis inducer. Showed broad antiproliferative activity against various tumor cell lines. Selectively inhibits T lymphocyte production of TNF-α. Upregulates endothelial nitric oxide synthase (eNOS; NOS III). Abrogates tumor angiogenesis in vivo.

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4-Chloro-3,5-xylenol ≥98%

Supplier: Thermo Fisher Scientific

4-Chloro-3,5-xylenol ≥98%

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Multidishes, non treated, Nunc™

Supplier: Thermo Fisher Scientific

PS, non treated, with lid, sterile.

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D-erythro-Sphingosine ≥98% (by TLC)

Supplier: ENZO LIFE SCIENCES

Common component of cell membranes, often as phosphatidyl conjugates. Is a potent (IC50=1-3 µM) and selective inhibitor of protein kinase C. Inhibition is competitive with diacylglycerol, phorbol dibutyrate and Ca2+ and it also inhibits PKC activation by other lipids. It acts on an equimolar basis with 1,2-dioleoylglycerol and does not affect other kinases such as MLCK and PKA. It is active in intact cells and has been identified as an endogenous constituent in HL-60 cells, neutrophils, rat liver, and brain and mouse tissues. Other activities include inhibition of phosphatidate phosphohydrolase, Na+,K+-ATPase, CTP:phosphocholine cytidylyltransferase, calmodulin-dependent enzymes, binding of factor VII to tissue factor, binding of thyrotropin releasing hormone to its receptor and activation of EGF receptor kinase, phospholipase D and casein kinase II.