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Vinblastine

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Vinblastine is a chemical compound used in laboratory research. It is a mitotic inhibitor, which means it interferes with the process of cell division. Vinblastine is commonly used in cell biology and cancer research studies.

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Lab products found in correlation

Colcemid, by Thermo Fisher Scientific (2 mentions) Reversine, by Selleck Chemicals (2 mentions) Camptothecin, by Selleck Chemicals (2 mentions) Dmem glutamax, by Thermo Fisher Scientific (2 mentions) Atm inhibitor ku55933, by Bio-Techne (2 mentions) Hesperadin, by Selleck Chemicals (2 mentions) Taxol, by AG Scientific (2 mentions) Dimethylenastron, by AG Scientific (2 mentions)

2 protocols using vinblastine

1

Fibroblast and Cancer Cell Culture Protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human IMR-90 primary lung fibroblasts (ATCC) and their derivatives were grown in Glutamax-DMEM (Gibco) supplemented with 0.1 mM nonessential Amino Acids and 15% Fetal Bovine Serum. HT1080 6TG cells were grown in Glutamax-DMEM supplemented with 0.1 mM Nonessential Amino Acids and 10% Bovine Growth Serum. All cells were grown at 7.5% CO2 and 3% O2. Colcemid (Life Technologies), Taxol (A. G. Scientific), vinblastine (A. G. Scientific), dimethylenastron (A. G. Scientific), hesperadin (Selleck), reversine (Selleck) and camptothecin (Selleck) were used at indicated concentration. ATM inhibitor (KU-55933) (Tocris) was used at 10 μM. FACS analysis was performed as described27 . Cells were tested for mycoplasma contamination and found negative.
Hayashi M.T., Cesare A.J., Rivera T, & Karlseder J. (2015). Cell Death During Crisis Is Mediated by Mitotic Telomere Deprotection. Nature, 522(7557), 492-496.
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2

Fibroblast and Cancer Cell Culture Protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human IMR-90 primary lung fibroblasts (ATCC) and their derivatives were grown in Glutamax-DMEM (Gibco) supplemented with 0.1 mM nonessential Amino Acids and 15% Fetal Bovine Serum. HT1080 6TG cells were grown in Glutamax-DMEM supplemented with 0.1 mM Nonessential Amino Acids and 10% Bovine Growth Serum. All cells were grown at 7.5% CO2 and 3% O2. Colcemid (Life Technologies), Taxol (A. G. Scientific), vinblastine (A. G. Scientific), dimethylenastron (A. G. Scientific), hesperadin (Selleck), reversine (Selleck) and camptothecin (Selleck) were used at indicated concentration. ATM inhibitor (KU-55933) (Tocris) was used at 10 μM. FACS analysis was performed as described27 . Cells were tested for mycoplasma contamination and found negative.
Hayashi M.T., Cesare A.J., Rivera T, & Karlseder J. (2015). Cell Death During Crisis Is Mediated by Mitotic Telomere Deprotection. Nature, 522(7557), 492-496.
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