You Searched For: Daunorubicin+hydrochloride

Catalog Number: (ENZOALX380043M010)

Supplier: ENZO LIFE SCIENCES

Description: Antitumor antibiotic.

UOM: 1 * 10 mg

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Catalog Number: (1164700.)

Supplier: 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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Catalog Number: (ENZOALX380260M005)

Supplier: 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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Supplier: MP Biomedicals

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

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Catalog Number: (BOSSBS-7953R-A680)

Supplier: 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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Catalog Number: (ENZOBMLPI1100010)

Supplier: 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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Catalog Number: (BOSSBS-7953R-HRP)

Supplier: 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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Catalog Number: (BOSSBS-7953R-A750)

Supplier: 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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Catalog Number: (PRSI79-673)

Supplier: 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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Catalog Number: (131105-25G)

Supplier: SIGMA-ALDRICH MICROSCOPY

Description: 3, 6-Diaminoacridine hydrochloride has been used for studying cation transfer at the liquid–liquid interface. An intercalating dye.

UOM: 1 * 25 g

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Supplier: 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).

Catalog Number: (361526-1G)

Supplier: SIGMA ALDRICH MICROSCOPY

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

UOM: 1 * 1 g

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Catalog Number: (P3750-25G)

Supplier: SIGMA-ALDRICH MICROSCOPY

Description: This is the pure, principal component of mixtures commonly referred to as Basic Fuchsin.

UOM: 1 * 25 g

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Supplier: SIGMA-ALDRICH MICROSCOPY

Description: In living mice, acriflavine hydrochloride has been used in the confocal laser endomicroscopy to check the crypt structure in mucosa. It has also been used in Neurospora strain selection by checking the acriflavine resistance.

Catalog Number: (0958-500G)

Supplier: VWR Chemicals

Description: L(+)-Ornithine hydrochloride ≥99%

UOM: 1 * 500 g

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Catalog Number: (247405-5G)

Supplier: SIGMA-ALDRICH MICROSCOPY

Description: Tricarbocyanine laser dye intermediate

UOM: 1 * 5 g

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