Esta buscando: Doxorubicin+hydrochloride

Numero del catalogo: (PHR1789-200MG)

Proveedor: Merck

Descripción: Organic Standard, Doxorubicin Hydrochloride

UOM: 1 * 200 mg

Promoción

Proveedor: TCI

Descripción: Doxorubicin hydrochloride ≥95.0% (by HPLC)

Certificados

Proveedor: Apollo Scientific

Descripción: Inhibitor of RNA synthesis.

Proveedor: ENZO LIFE SCIENCES

Descripción: Topoisomerase inhibitor

New Product

Numero del catalogo: (1225703.)

Proveedor: USP

Descripción: 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 * 50 mg

Promoción

Numero del catalogo: (ICNA0215910110)

Proveedor: MP Biomedicals

Descripción: Doxorubicin Hydrochloride is a chemotherapeutic, antitumour, immunosuppressive, and antibiotic agent.

UOM: 1 * 10 mg

FDS Promoción

Proveedor: Cayman Chemical

Descripción: Doxorubicin is an anthracycline anti-tumour antibiotic which involves in inhibition of DNA topoisomerase II by inducing double-stranded DNA breaks. It is also involved in the inhibition of nucleic acid synthesis by intercalating within DNA. The accumulation of the p53 tumour suppressor protein leads to the apoptosis in cells.

Proveedor: Thermo Fisher Scientific

Descripción: Doxorubicin hydrochloride is an anti-tumour, anti-neoplastic and anti-biotic agent that inhibits DNA topoisomerase II. It also inhibits nucleic acid synthesis and induces apoptosis.

FDS Certificados

Numero del catalogo: (PROOBP990)

Proveedor: LGC Standards PROMOCHEM

Descripción: Organic Standard, Doxorubicin hydrochloride assay standard

UOM: 1 * 100 mg

Promoción

Numero del catalogo: (API-05)

Proveedor: G-Biosciences

Descripción: Apoptosis is commonly defined as programmed mechanism of cell death and is a highly regulated process that can be initiated by a variety of internal and external stimuli (inducers).

UOM: 1 * 50 µl

Promoción

Numero del catalogo: (BOSSBS-3523R-HRP)

Proveedor: Bioss

Descripción: Phosphorylates MAP kinase p38. Seems to be active only in mitosis. May also play a role in the activation of lymphoid cells. When phosphorylated, forms a complex with TP53, leading to TP53 destabilization and attenuation of G2/M checkpoint during doxorubicin-induced DNA damage.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-7953R-HRP)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (API-16S)

Proveedor: G-Biosciences

Descripción: Apoptosis inducers are used for induction of apoptosis in cultured cells. The selection of apoptosis inducers include actinomycin D, camptothecin, cycloheximide, dexamethasone, doxorubicin and etoposide.

UOM: 1 * 1 SET

Promoción

Numero del catalogo: (BOSSBS-7953R-A680)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-7953R-A750)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (PRSI5815)

Proveedor: ProSci Inc.

Descripción: FOXO4 Antibody: FOXO4 is a ubiquitously expressed protein member of a subfamily of the forkhead homeotic gene family of transcription factors and shuttles between the cytoplasm and nucleus. FOXO transcription factors are key players of cell fate decisions, metabolism, stress resistance, tumor suppression and are regulated by growth factors, oxidative stress or nutrient deprivation. In the absence of PI3K/AKT activation, FOXO4 localizes in the nucleus where it functions as a transcription factor. FOXO4 can also be phosphorylated by JNK following induction of reactive oxygen species (ROS), resulting in transcriptional activation and the induction of a negative feedback mechanism to counteract the ROS. It is through this mechanism that FOXO4 is thought to sensitize cancer cells to doxorubicin-mediated toxicity.

UOM: 1 * 100 µG

Promoción