trypan blue dye exclusion test Search Results


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Erma Inc trypan blue dye exclusion
The proliferation of gingival fibroblasts stimulated with or without LPS or cyclosporine A in the culture with D-MEM plus serum. After semi-confluent cells were cultured in D-MEM containing 1% serum for 24 h, cells were treated with or without 200 ng/mL of cyclosporine A or 1 μg/mL of LPS in D-MEM containing 5% serum for 24 or 48 h. The total number of cells was measured with <t>Trypan</t> <t>Blue</t> <t>dye</t> <t>exclusion</t> using a blood corpuscle counting chamber and an optical microscope. The fold change from the negative control was calculated. Data are presented as means ± SEM. Welch’s t -test with Bonferroni’s correction was used for statistics. * p < 0.05 indicates a statistically significant difference. n = 4. Cs A, cyclosporine A.
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Lindl GmbH trypan blue (0.4%) dye exclusion technique
The proliferation of gingival fibroblasts stimulated with or without LPS or cyclosporine A in the culture with D-MEM plus serum. After semi-confluent cells were cultured in D-MEM containing 1% serum for 24 h, cells were treated with or without 200 ng/mL of cyclosporine A or 1 μg/mL of LPS in D-MEM containing 5% serum for 24 or 48 h. The total number of cells was measured with <t>Trypan</t> <t>Blue</t> <t>dye</t> <t>exclusion</t> using a blood corpuscle counting chamber and an optical microscope. The fold change from the negative control was calculated. Data are presented as means ± SEM. Welch’s t -test with Bonferroni’s correction was used for statistics. * p < 0.05 indicates a statistically significant difference. n = 4. Cs A, cyclosporine A.
Trypan Blue (0.4%) Dye Exclusion Technique, supplied by Lindl GmbH, 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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SERVA Electrophoresis trypan blue exclusion dye serva
The proliferation of gingival fibroblasts stimulated with or without LPS or cyclosporine A in the culture with D-MEM plus serum. After semi-confluent cells were cultured in D-MEM containing 1% serum for 24 h, cells were treated with or without 200 ng/mL of cyclosporine A or 1 μg/mL of LPS in D-MEM containing 5% serum for 24 or 48 h. The total number of cells was measured with <t>Trypan</t> <t>Blue</t> <t>dye</t> <t>exclusion</t> using a blood corpuscle counting chamber and an optical microscope. The fold change from the negative control was calculated. Data are presented as means ± SEM. Welch’s t -test with Bonferroni’s correction was used for statistics. * p < 0.05 indicates a statistically significant difference. n = 4. Cs A, cyclosporine A.
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Coriell Institute for Medical Research trypan blue exclusion dye
The proliferation of gingival fibroblasts stimulated with or without LPS or cyclosporine A in the culture with D-MEM plus serum. After semi-confluent cells were cultured in D-MEM containing 1% serum for 24 h, cells were treated with or without 200 ng/mL of cyclosporine A or 1 μg/mL of LPS in D-MEM containing 5% serum for 24 or 48 h. The total number of cells was measured with <t>Trypan</t> <t>Blue</t> <t>dye</t> <t>exclusion</t> using a blood corpuscle counting chamber and an optical microscope. The fold change from the negative control was calculated. Data are presented as means ± SEM. Welch’s t -test with Bonferroni’s correction was used for statistics. * p < 0.05 indicates a statistically significant difference. n = 4. Cs A, cyclosporine A.
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The proliferation of gingival fibroblasts stimulated with or without LPS or cyclosporine A in the culture with D-MEM plus serum. After semi-confluent cells were cultured in D-MEM containing 1% serum for 24 h, cells were treated with or without 200 ng/mL of cyclosporine A or 1 μg/mL of LPS in D-MEM containing 5% serum for 24 or 48 h. The total number of cells was measured with Trypan Blue dye exclusion using a blood corpuscle counting chamber and an optical microscope. The fold change from the negative control was calculated. Data are presented as means ± SEM. Welch’s t -test with Bonferroni’s correction was used for statistics. * p < 0.05 indicates a statistically significant difference. n = 4. Cs A, cyclosporine A.

Journal: Diseases

Article Title: Cyclosporine A Causes Gingival Overgrowth by Promoting Entry into the S Phase at the G1/S Cell Cycle Checkpoint in Gingival Fibroblasts Exposed to Lipopolysaccharide

doi: 10.3390/diseases12120322

Figure Lengend Snippet: The proliferation of gingival fibroblasts stimulated with or without LPS or cyclosporine A in the culture with D-MEM plus serum. After semi-confluent cells were cultured in D-MEM containing 1% serum for 24 h, cells were treated with or without 200 ng/mL of cyclosporine A or 1 μg/mL of LPS in D-MEM containing 5% serum for 24 or 48 h. The total number of cells was measured with Trypan Blue dye exclusion using a blood corpuscle counting chamber and an optical microscope. The fold change from the negative control was calculated. Data are presented as means ± SEM. Welch’s t -test with Bonferroni’s correction was used for statistics. * p < 0.05 indicates a statistically significant difference. n = 4. Cs A, cyclosporine A.

Article Snippet: We counted the total number of cells to evaluate cell proliferation with Trypan Blue dye exclusion using a blood corpuscle counting chamber (Burker-Turk deep 1/10 mm, ERMA Inc., Tokyo, Japan) and observed the cellular morphology using an optical microscope (Nikon TE300 Inverted Tissue Culture Microscope, Tokyo, Japan; magnification, 40×).

Techniques: Cell Culture, Microscopy, Negative Control