emv inhibitors bisindolylmaleimide i  (Millipore)


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    Name:
    Bisindolylmaleimide IV
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    Catalog Number:
    b3306
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    Millipore emv inhibitors bisindolylmaleimide i
    Bisindolylmaleimide IV

    https://www.bioz.com/result/emv inhibitors bisindolylmaleimide i/product/Millipore
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    emv inhibitors bisindolylmaleimide i - by Bioz Stars, 2020-09
    93/100 stars

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    1) Product Images from "Chloramidine/Bisindolylmaleimide-I-Mediated Inhibition of Exosome and Microvesicle Release and Enhanced Efficacy of Cancer Chemotherapy"

    Article Title: Chloramidine/Bisindolylmaleimide-I-Mediated Inhibition of Exosome and Microvesicle Release and Enhanced Efficacy of Cancer Chemotherapy

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms18051007

    Pharmacological inhibition of EMV release from PC3 cells is highest with Cl-amidine, bisindolylmaleimide-I, and imipramine. ( A ) Using NTA, the most significant inhibition of EMV release from PC3 cells after 24 h was observed in the presence of Cl-amidine, bisindolylmaleimide-I, and imipramine. After 24 h, none of the inhibitors caused any significant reduction in cell viability, ( B ) except for d -pantethine. The experiments were repeated three times, and the data presented are mean ± SEM of the results. (* p ≤ 0.05; **** p ≤ 0.0001).
    Figure Legend Snippet: Pharmacological inhibition of EMV release from PC3 cells is highest with Cl-amidine, bisindolylmaleimide-I, and imipramine. ( A ) Using NTA, the most significant inhibition of EMV release from PC3 cells after 24 h was observed in the presence of Cl-amidine, bisindolylmaleimide-I, and imipramine. After 24 h, none of the inhibitors caused any significant reduction in cell viability, ( B ) except for d -pantethine. The experiments were repeated three times, and the data presented are mean ± SEM of the results. (* p ≤ 0.05; **** p ≤ 0.0001).

    Techniques Used: Inhibition

    Cl-amidine and bisindolylmaleimide-1-mediated inhibition of EMV release increases the apoptosis of PC3 and MCF-7 cells treated with 5-FU. The Guava Viacount Cell Death Assay shows that PC3 and MCF-7 cells that were given 5-FU together with Cl-amidine, bisindolylmaleimide-I, or with a combination of Cl-amidine and bisindolylmaleimide-I, had significantly reduced levels of cell viability within 24 h compared to PC3 and MCF-7 cells receiving no EMV inhibitors and given only 5-FU. Bisindolylmaleimide-I and Cl-amidine had no significant effect on cell viability on their own. Data presented are the mean ± SEM of three independent experiments performed in triplicate (** p ≤ 0.01; *** p ≤ 0.001; **** p ≤ 0.0001 were considered statistically significant compared to the drug-treated control in the absence of inhibitors).
    Figure Legend Snippet: Cl-amidine and bisindolylmaleimide-1-mediated inhibition of EMV release increases the apoptosis of PC3 and MCF-7 cells treated with 5-FU. The Guava Viacount Cell Death Assay shows that PC3 and MCF-7 cells that were given 5-FU together with Cl-amidine, bisindolylmaleimide-I, or with a combination of Cl-amidine and bisindolylmaleimide-I, had significantly reduced levels of cell viability within 24 h compared to PC3 and MCF-7 cells receiving no EMV inhibitors and given only 5-FU. Bisindolylmaleimide-I and Cl-amidine had no significant effect on cell viability on their own. Data presented are the mean ± SEM of three independent experiments performed in triplicate (** p ≤ 0.01; *** p ≤ 0.001; **** p ≤ 0.0001 were considered statistically significant compared to the drug-treated control in the absence of inhibitors).

    Techniques Used: Inhibition

    Nanoparticle tracking analysis (NTA) of exosomes and microvesicles (EMVs) released from PC3 cells in the presence of a range of EMV inhibitors. Plots presenting NTA analysis show the concentration of vesicles (0–900 nm in diameter) released from PC3 cells in the absence of any EMV inhibitors ( A ); In ( B ) the EMVs are shown to comprise exosomes and microvesicles (MVs) by electron microscopy, by Western blotting (for CD63 expression), and by the degree of phosphatidylserine (PS) exposition. NTA analysis for released EMVs from PC3 cells are presented in the presence of Cl-amidine ( C ); bisindolylmaleimide-I ( D ); and imipramine ( E ). Vesicles outside the size range of 0–900 nm were excluded to avoid including larger vesicles such as MV aggregates or apoptotic bodies. The experiment was repeated three times in total (error bars ± SEM, indicated in red).
    Figure Legend Snippet: Nanoparticle tracking analysis (NTA) of exosomes and microvesicles (EMVs) released from PC3 cells in the presence of a range of EMV inhibitors. Plots presenting NTA analysis show the concentration of vesicles (0–900 nm in diameter) released from PC3 cells in the absence of any EMV inhibitors ( A ); In ( B ) the EMVs are shown to comprise exosomes and microvesicles (MVs) by electron microscopy, by Western blotting (for CD63 expression), and by the degree of phosphatidylserine (PS) exposition. NTA analysis for released EMVs from PC3 cells are presented in the presence of Cl-amidine ( C ); bisindolylmaleimide-I ( D ); and imipramine ( E ). Vesicles outside the size range of 0–900 nm were excluded to avoid including larger vesicles such as MV aggregates or apoptotic bodies. The experiment was repeated three times in total (error bars ± SEM, indicated in red).

    Techniques Used: Concentration Assay, Electron Microscopy, Western Blot, Expressing

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    Article Snippet: .. Alsterpaullone (Calbiochem) was used at a final concentration of 10 μM, bisindolylmaleimide IX (Calbiochem) at a final concentration of 2 μM, bisindolylmaleimide I (Calbiochem) at a final concentration of 4 μM, lithium chloride at a final concentration of 50 mM, cycloheximide (Sigma) at a final concentration of 30 μg/ml, puromycin at a final concentration of 1.5 μg/ml, and MG132 at a final concentration of 10 μM. .. Cells were irradiated in culture medium with 7.5 grays using a 60 Co γ source with a dose rate of 2 grays/min.

    Activation Assay:

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