efficient navigation (zen)-black edition software Search Results


efficient navigation (zen)-black edition software  (Carl Zeiss)
90
Carl Zeiss efficient navigation (zen)-black edition software
Efficient Navigation (Zen) Black Edition Software, supplied by Carl Zeiss, 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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zen software zen 2011 sp4 black edition  (Carl Zeiss)
90
Carl Zeiss zen software zen 2011 sp4 black edition
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
Zen Software Zen 2011 Sp4 Black Edition, supplied by Carl Zeiss, 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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Average 90 stars, based on 1 article reviews
zen software zen 2011 sp4 black edition - by Bioz Stars, 2026-08
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flamruss 101® lamp black carbon black  (DeGussa Corporation)
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DeGussa Corporation flamruss 101® lamp black carbon black
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
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black resist ck-a143b resist  (FUJIFILM)
90
FUJIFILM black resist ck-a143b resist
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
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paliogen® black l0086  (BASF)
90
BASF paliogen® black l0086
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
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black particles (4)  (BASF)
90
BASF black particles (4)
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
Black Particles (4), supplied by BASF, 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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black particles (4) - by Bioz Stars, 2026-08
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carbon black n990  (Cancarb Limited)
90
Cancarb Limited carbon black n990
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
Carbon Black N990, supplied by Cancarb Limited, 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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carbon black  (Denka Co Ltd)
90
Denka Co Ltd carbon black
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
Carbon Black, supplied by Denka Co 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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sudan black b  (Valiant Co Ltd)
96
Valiant Co Ltd sudan black b
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
Sudan Black B, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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carbon black powder  (Nanografi Advanced Materials)
92
Nanografi Advanced Materials carbon black powder
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
Carbon Black Powder, supplied by Nanografi Advanced Materials, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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solvent black 29 orasol black x55  (BASF)
90
BASF solvent black 29 orasol black x55
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
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carbon black carbon black  (Cabot Corporation)
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Cabot Corporation carbon black carbon black
Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl <t>Zeiss;</t> <t>ZEN-software).</t> For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).
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Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl Zeiss; ZEN-software). For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).

Journal: Frontiers in Bioengineering and Biotechnology

Article Title: Enhancement of Intracellular Calcium Ion Mobilization by Moderately but Not Highly Positive Material Surface Charges

doi: 10.3389/fbioe.2020.01016

Figure Lengend Snippet: Dynamic Ca 2+ mobilization in vital fluo-3 loaded MG-63s growing on amino polymers, extracellular matrix (ECM)/peptide motifs and polyelectrolyte multilayers (PEM) in the time frame 0–480 s. The positive control PPAAm (also an amino polymer) and the negative control Ti are embedded for the respective experiment. Shown are time courses of the mean fluorescence intensity of cells (MFI C ) over 8 min: First, the basal Ca 2+ signal is recorded for 180 s. At 180 s the cells are stimulated with ATP (arrowheads) and the Ca 2+ signal is detected (LSM780, Carl Zeiss; ZEN-software). For statistical analyses of the basal MFI, values of the time points 0–170 s are used. For analyses of the MFI after ATP stimulation, values of the time points 190–240 s are used (highlighted in grey). MFI C values are normalized to the mean cell area after 24 h. (Statistics: Kruskal–Wallis and Dunn’s multiple comparison test, p < 0.05; mean ± sem; n ≥ 3 independent approaches, per time point ≥ 30 cells; * indicates significance of modification x to Ti and # significance to PPAAm).

Article Snippet: Oil DIC M27) and the ZEN software (ZEISS efficient navigation, ZEN 2011 SP4, black edition, Carl Zeiss).

Techniques: Positive Control, Polymer, Negative Control, Fluorescence, Software, Comparison, Modification