diff-quik solution kit Search Results


diff quik solution kit  (Sysmex Corporation)
86
Sysmex Corporation diff quik solution kit
Diff Quik Solution Kit, supplied by Sysmex Corporation, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/diff quik solution kit/product/Sysmex Corporation
Average 86 stars, based on 1 article reviews
diff quik solution kit - by Bioz Stars, 2026-06
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diffquick kit solutions  (Medion Diagnostics)
90
Medion Diagnostics diffquick kit solutions
Diffquick Kit Solutions, supplied by Medion Diagnostics, 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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diff quick staining solution kit  (Medion Diagnostics)
90
Medion Diagnostics diff quick staining solution kit
Diff Quick Staining Solution Kit, supplied by Medion Diagnostics, 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
diff quick staining solution kit - by Bioz Stars, 2026-06
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diff-quik stain kit  (Becton Dickinson)
90
Becton Dickinson diff-quik stain kit
Diff Quik Stain Kit, supplied by Becton Dickinson, 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
diff-quik stain kit - by Bioz Stars, 2026-06
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diff-quik staining  (Polysciences inc)
90
Polysciences inc diff-quik staining
Diff Quik Staining, supplied by Polysciences inc, 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
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cell proliferation assay kit tetracolor one  (Seikagaku corporation)
90
Seikagaku corporation cell proliferation assay kit tetracolor one
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
Cell Proliferation Assay Kit Tetracolor One, supplied by Seikagaku corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cell proliferation assay kit tetracolor one/product/Seikagaku corporation
Average 90 stars, based on 1 article reviews
cell proliferation assay kit tetracolor one - by Bioz Stars, 2026-06
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purelink rna mini kit  (Thermo Fisher)
99
Thermo Fisher purelink rna mini kit
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
Purelink Rna Mini Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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purelink rna mini kit - by Bioz Stars, 2026-06
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0.05 % toluidine blue solution (ph 4.1)  (FUJIFILM)
90
FUJIFILM 0.05 % toluidine blue solution (ph 4.1)
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
0.05 % Toluidine Blue Solution (Ph 4.1), supplied by FUJIFILM, 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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700 lsm confocal microscope  (Carl Zeiss)
90
Carl Zeiss 700 lsm confocal microscope
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
700 Lsm Confocal Microscope, 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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matrigel basement membrane matrix  (Becton Dickinson)
90
Becton Dickinson matrigel basement membrane matrix
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
Matrigel Basement Membrane Matrix, supplied by Becton Dickinson, 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
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matrigel invasion chamber transwell polycarbonate membrane inserts  (Corning Life Sciences)
90
Corning Life Sciences matrigel invasion chamber transwell polycarbonate membrane inserts
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
Matrigel Invasion Chamber Transwell Polycarbonate Membrane Inserts, supplied by Corning Life Sciences, 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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celltiter-glo luminescence cell viability assay kit  (Promega)
90
Promega celltiter-glo luminescence cell viability assay kit
Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited <t>proliferation</t> of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by <t>TetraColor</t> One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.
Celltiter Glo Luminescence Cell Viability Assay Kit, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/celltiter-glo luminescence cell viability assay kit/product/Promega
Average 90 stars, based on 1 article reviews
celltiter-glo luminescence cell viability assay kit - by Bioz Stars, 2026-06
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Image Search Results


Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited proliferation of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by TetraColor One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.

Journal: PLoS ONE

Article Title: Anti-Tumor Activity of a Novel HS-Mimetic-Vascular Endothelial Growth Factor Binding Small Molecule

doi: 10.1371/journal.pone.0039444

Figure Lengend Snippet: Cells were seeded in ACEA's 96× e-plate™ at a density of 5×10 3 cells per well, and continuously monitored using the RT-CES system up to 24 h, at which point Compound 8 (2 to 50 µM) was added. The cell index is plotted against time. The arrow indicates the time of the addition of compound 8 . Data represent the mean values ± S.D. for three identical wells from three independent experiments. B , compound 8 poorly inhibited proliferation of UV♀2 under serum-replete conditions (FBS), but potently inhibited VEGF-dependent proliferation of UV♀2 cells as analysed by TetraColor One assay. Results were normalised to DMSO controls. Data represent mean values ± SD for three independent experiments. * P <0.05 versus control. ** P <0.01 versus control. C , compound 8 inhibits VEGF-stimulated proliferation of human vascular endothelial cells. HUVEC cells were seeded on 6-well plates at a density of approximately 1×10 5 cells/well in M200 medium supplement with LSGS (Low serum growth Supplement). The next day cells were stimulated with 10 ng/mL of VEGF in the presence or absence of 1 µM and 10 µM compound 8 . After 48 hrs, Alamar Blue was added directly into culture media at a final concentration of 10% and the plate was returned to the incubator. Optical density (OD) of the plate was measured at 540 and 630 nm. As a negative control, AB was added to medium without cells.

Article Snippet: The cell proliferation assay kit Tetracolor One was obtained from Seikagaku Corp. (Tokyo, Japan) and the Diff-Quick solution was from International Reagent Corp. (Kobe, Japan).

Techniques: Control, Concentration Assay, Negative Control