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  • 90
    Avidin Ltd singlecellprotecttm
    Singlecellprotecttm, supplied by Avidin Ltd, used in various techniques. Bioz Stars score: 90/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avidin Ltd amino trifluoro phtalimide analogs
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    Avidin Ltd 665 member library
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    Avidin Ltd 9 fluorenylmethoxycarbonyl
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    Avidin Ltd male scid mice
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    Avidin Ltd research compound q50
    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with <t>Q50</t> (A,C) invade the surrounding matrix with similar speeds as the control cultures
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    Avidin Ltd fmoc gp cox
    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with <t>Q50</t> (A,C) invade the surrounding matrix with similar speeds as the control cultures
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    Avidin Ltd interests pgl
    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with <t>Q50</t> (A,C) invade the surrounding matrix with similar speeds as the control cultures
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    Avidin Ltd ivc system
    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with <t>Q50</t> (A,C) invade the surrounding matrix with similar speeds as the control cultures
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    Avidin Ltd lgp
    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with <t>Q50</t> (A,C) invade the surrounding matrix with similar speeds as the control cultures
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    Avidin Ltd singlecellprotect
    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with <t>Q50</t> (A,C) invade the surrounding matrix with similar speeds as the control cultures
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    Avidin Ltd z devd aluc substrate
    Differentiation of promyelocytic leukemia cells is followed by apoptotic cell death. Differentiation of HL-60 cells was accompanied by cell death detected by RealTime-Glo TM MT Cell Viability Assay ( A ). The depolarization of the mitochondrial membrane potential (MMP) ( B ), activation of caspase-3 ( C ), and the cleavage of <t>Z-DEVD-aLuc</t> ( D ) were observed after 24 h. Cell cycle was arrested in G2/M detected after 72 h incubation ( E ). Finally, as a proof of massive cell death, we showed both the appearance of the hypodiploid apoptotic cells in the sub-G1 population ( F ) and the leakage of the lactate-dehydrogenase (LDH) into the supernatant ( G ) after 72 h incubation. Data are shown as arithmetic mean values ± standard deviation from triplicate experiments. Statistical significance was calculated in relation to untreated cells and set to * p
    Z Devd Aluc Substrate, supplied by Avidin Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with Q50 (A,C) invade the surrounding matrix with similar speeds as the control cultures

    Journal: Physical biology

    Article Title: Invasion from a cell aggregate – the roles of active cell motion and mechanical equilibrium

    doi: 10.1088/1478-3975/9/1/016010

    Figure Lengend Snippet: GBM1 (A,B) and U87 (C,D) cells substantially invade collagen gels after one day in culture. The initial invasion patterns are independent of cell division: cells treated with Q50 (A,C) invade the surrounding matrix with similar speeds as the control cultures

    Article Snippet: To block cell divisions, we utilized the research compound Q50 (Avidin Ltd, Hungary).

    Techniques:

    Differentiation of promyelocytic leukemia cells is followed by apoptotic cell death. Differentiation of HL-60 cells was accompanied by cell death detected by RealTime-Glo TM MT Cell Viability Assay ( A ). The depolarization of the mitochondrial membrane potential (MMP) ( B ), activation of caspase-3 ( C ), and the cleavage of Z-DEVD-aLuc ( D ) were observed after 24 h. Cell cycle was arrested in G2/M detected after 72 h incubation ( E ). Finally, as a proof of massive cell death, we showed both the appearance of the hypodiploid apoptotic cells in the sub-G1 population ( F ) and the leakage of the lactate-dehydrogenase (LDH) into the supernatant ( G ) after 72 h incubation. Data are shown as arithmetic mean values ± standard deviation from triplicate experiments. Statistical significance was calculated in relation to untreated cells and set to * p

    Journal: International Journal of Molecular Sciences

    Article Title: Imidazo[1,2-b]pyrazole-7-Carboxamide Derivative Induces Differentiation-Coupled Apoptosis of Immature Myeloid Cells Such as Acute Myeloid Leukemia and Myeloid-Derived Suppressor Cells

    doi: 10.3390/ijms21145135

    Figure Lengend Snippet: Differentiation of promyelocytic leukemia cells is followed by apoptotic cell death. Differentiation of HL-60 cells was accompanied by cell death detected by RealTime-Glo TM MT Cell Viability Assay ( A ). The depolarization of the mitochondrial membrane potential (MMP) ( B ), activation of caspase-3 ( C ), and the cleavage of Z-DEVD-aLuc ( D ) were observed after 24 h. Cell cycle was arrested in G2/M detected after 72 h incubation ( E ). Finally, as a proof of massive cell death, we showed both the appearance of the hypodiploid apoptotic cells in the sub-G1 population ( F ) and the leakage of the lactate-dehydrogenase (LDH) into the supernatant ( G ) after 72 h incubation. Data are shown as arithmetic mean values ± standard deviation from triplicate experiments. Statistical significance was calculated in relation to untreated cells and set to * p

    Article Snippet: We diluted Z-DEVD-aLuc substrate (10 mM stock in DMSO, Avidin Ltd.) in 1X Assay Buffer, stock Assay Buffer 10X (200 mM HEPES, pH 7.4, 1% CHAPS, 50 mM DTT, 20 mM EDTA) was stored at −20°C and it was diluted prior use freshly in sterile water.

    Techniques: Viability Assay, Activation Assay, Incubation, Standard Deviation