Votre recherche pour: Daunorubicin+hydrochloride

Référence Produit: (ENZOALX380043M010)

Fournisseur: ENZO LIFE SCIENCES

Description: Antitumor antibiotic.

UOM: 1 * 10 mg

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Référence Produit: (1164700.)

Fournisseur: USP

Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

UOM: 1 * 200 mg

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Référence Produit: (ENZOALX380260M005)

Fournisseur: ENZO LIFE SCIENCES

Description: More potent, lipophilic and antineoplastic analog of daunorubicin. DNA-damaging effect includes DNA oxidation and methylation, DNA intercalation, inhibition of DNA synthesis, induction of DNA strand breaks and delay of cell cycle progression. Inhibitor of topoisomerase IIα. Produces endonucleolytic cleavage and is a marker of apoptosis.

UOM: 1 * 5 mg

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Fournisseur: MP Biomedicals

Description: Soluble in water, methanol, aqueous alcohols. Practically insoluble in chloroform, ether, benzene.

Certificats.

Référence Produit: (ENZOBMLPI1100010)

Fournisseur: ENZO LIFE SCIENCES

Description: A potent irreversible mechanism based serine protease inhibitor. Inhibits granzymes A, B, and H, cathepsin G, neutrophil elastase and proteinase 3. Inhibits activation of neutral sphingomyelinase and apoptosis triggered by daunorubicin as well as camptothecin-induced apoptosis in HL-60 cells. Inhibits migration of eosinophils through basement membrane components in vitro.

UOM: 1 * 10 mg

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Référence Produit: (BOSSBS-7953R-A680)

Fournisseur: Bioss

Description: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).

UOM: 1 * 100 µl

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Référence Produit: (BOSSBS-7953R-HRP)

Fournisseur: Bioss

Description: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).

UOM: 1 * 100 µl

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Référence Produit: (BOSSBS-7953R-A750)

Fournisseur: Bioss

Description: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).

UOM: 1 * 100 µl

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Référence Produit: (PRSI79-673)

Fournisseur: ProSci Inc.

Description: Xenobiotic transporter that may play an important role in the exclusion of xenobiotics from the brain. May be involved in brain-to-blood efflux. Appears to play a major role in the multidrug resistance phenotype of several cancer cell lines. When overexpressed, the transfected cells become resistant to mitoxantrone, daunorubicin and doxorubicin, display diminished intracellular accumulation of daunorubicin, and manifest an ATP-dependent increase in the efflux of rhodamine 123.

UOM: 1 * 100 µG

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Fournisseur: Merck

Description: Phenethylbiguanide hydrochloride, Supelco®

Référence Produit: (247405-5G)

Fournisseur: SIGMA ALDRICH MICROSCOPY

Description: Tricarbocyanine laser dye intermediate

UOM: 1 * 5 g

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Référence Produit: (361526-1G)

Fournisseur: SIGMA ALDRICH MICROSCOPY

Description: 2-(3-Aminophenylsulphonyl)ethanol hydrochloride 97%, Sigma-Aldrich®

UOM: 1 * 1 g

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Fournisseur: Merck

Description: 2'-Deoxycytidine hydrochloride, Supelco®

Fournisseur: SIGMA ALDRICH MICROSCOPY

Description: 5-([4,6-Dichlorotriazin-2-yl]amino)fluorescein hydrochloride has been used for labeling of yeast cells to study the adhesion of yeast cells to the digestive tract of sea bass (Dicentrarchus labrax) larvae and leopard grouper (Mycteroperca rosacea).

Fournisseur: Merck

Description: O-Methylhydroxylamine hydrochloride 97.5-102.5% (par titration argentométrique), LiChropur™ pour dérivatisation GC, Supelco®

Référence Produit: (43504-10G)

Fournisseur: Merck

Description: O-Ethylhydroxylamine hydrochloride 99.0-101.0% (par titration argentométrique), LiChropur™ pour dérivatisation GC, Supelco®

UOM: 1 * 10 g

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