caski hpv16 Search Results


98
ATCC hpv16 positive
Hpv16 Positive, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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caski  (ATCC)
97
ATCC caski
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Caski, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
ATCC caski cells
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Caski Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
ATCC human cc cell lines
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Human Cc Cell Lines, supplied by ATCC, 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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90
National Centre for Cell Science human cca caski cells (hpv16)
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Human Cca Caski Cells (Hpv16), supplied by National Centre for Cell Science, 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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93
ATCC control cell line cell line hpv infection infected hpv type atcc 45022 hpv 2a atcc 45150 hpv 6b atcc 45151 hpv 11 atcc 45113 hpv 16 atcc
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Control Cell Line Cell Line Hpv Infection Infected Hpv Type Atcc 45022 Hpv 2a Atcc 45150 Hpv 6b Atcc 45151 Hpv 11 Atcc 45113 Hpv 16 Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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95
ATCC hpv subtypes
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Hpv Subtypes, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
ZeptoMetrix corporation tv not detected 0810005cf herpes simplex virus ii zeptometrix tv not detected 08100060f hiv 1 zeptometrix tv not detected 0801032cf hpv 16 caski
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
Tv Not Detected 0810005cf Herpes Simplex Virus Ii Zeptometrix Tv Not Detected 08100060f Hiv 1 Zeptometrix Tv Not Detected 0801032cf Hpv 16 Caski, supplied by ZeptoMetrix corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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85
Addgene inc 5370100 cask nm 003688 image
The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis <t>of</t> <t>HPV-positive</t> cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, <t>CaSki,</t> and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.
5370100 Cask Nm 003688 Image, supplied by Addgene inc, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis of HPV-positive cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, CaSki, and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.

Journal: Cancers

Article Title: Targeted Disruption of E6/p53 Binding Exerts Broad Activity and Synergism with Paclitaxel and Topotecan against HPV-Transformed Cancer Cells

doi: 10.3390/cancers14010193

Figure Lengend Snippet: The cell-cycle arrest induced by Cpd12 occurs in the G1 phase. ( A ) The effects of Cpd12, the inactive small molecule Cpd3, or DMSO, on cell cycle modulation were evaluated by cytofluorimetric analysis of HPV-positive cervical (ME180 and MS751) and head-and-neck (SCC152) cancer cells treated for 24 h and then stained with PI. Bar graphs represent the percentage of cells in the different phases of the cell cycle (G0/G1, M, G2/S) as the mean of three independent experiments. ( B ) Cell-cycle distributions of HPV-positive cervical (ME180, MS751, HeLa, CaSki, and SiHa) and head-and-neck (SCC152) cancer cells treated with Cpd12 (50 µM) or DMSO for 24 h were determined through immunofluorescence assays. Cells in either the G0, G1, S, G2, or M phase were determined as a function of Ki67 and nuclear staining, and fluorescence intensities were quantified from maximum intensity projections of Z-stack images acquired with a 600× magnification. Total numbers of cells were: n DMSO = 463 and n Cpd12 = 304 for ME180 cells, n DMSO = 303 and n Cpd12 = 316 for MS751 cells, n DMSO = 314 and n Cpd12 = 267 for SCC152 cells, n DMSO = 303 and n Cpd12 = 270 for HeLa cells, n DMSO = 388 and n Cpd12 = 330 for CaSki cells, and n DMSO = 336 and n Cpd12 = 244 for SiHa cells. Nuclei were stained with DRAQ5. 2N: diploid DNA content, 4N: tetraploid DNA content.

Article Snippet: HPV-positive HeLa (HPV18), CaSki (HPV16), SiHa (HPV16), ME180 (HPV68), MS751 (HPV45), and HPV-negative C33A cervical cancer cells, HPV-positive SCC152 (HPV16) and HPV-negative FaDu head-and-neck cancer cells, and human foreskin fibroblasts (HFF) were all from the American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Staining, Immunofluorescence, Fluorescence

The Cpd12-induced rescue of p53 affects the migration capacity of HPV-transformed cells. ( A ) Confluent monolayers of HeLa, CaSki, and ME180 cervical cancer cells were scraped up two times and then treated with increasing concentration of Cpd12 (10, 25, and 50 µM) in low serum medium. The wound closure was monitored before treatment and after 12, 24, and 48 h, and representative images were taken using a bright-field inverted microscope (100× magnification). ( B ) HeLa cells were treated with Cpd12 (50 μM) for 24 h. Then, cell migration was evaluated by transwell assays after an incubation of other 24 h in Cpd12-free medium. Representative images of migrated cells fixed and colored with crystal violet were taken using a bright-field inverted microscope (100× magnification). In both panels, cells treated with DMSO or Cpd3 (50 μM) were included as negative controls.

Journal: Cancers

Article Title: Targeted Disruption of E6/p53 Binding Exerts Broad Activity and Synergism with Paclitaxel and Topotecan against HPV-Transformed Cancer Cells

doi: 10.3390/cancers14010193

Figure Lengend Snippet: The Cpd12-induced rescue of p53 affects the migration capacity of HPV-transformed cells. ( A ) Confluent monolayers of HeLa, CaSki, and ME180 cervical cancer cells were scraped up two times and then treated with increasing concentration of Cpd12 (10, 25, and 50 µM) in low serum medium. The wound closure was monitored before treatment and after 12, 24, and 48 h, and representative images were taken using a bright-field inverted microscope (100× magnification). ( B ) HeLa cells were treated with Cpd12 (50 μM) for 24 h. Then, cell migration was evaluated by transwell assays after an incubation of other 24 h in Cpd12-free medium. Representative images of migrated cells fixed and colored with crystal violet were taken using a bright-field inverted microscope (100× magnification). In both panels, cells treated with DMSO or Cpd3 (50 μM) were included as negative controls.

Article Snippet: HPV-positive HeLa (HPV18), CaSki (HPV16), SiHa (HPV16), ME180 (HPV68), MS751 (HPV45), and HPV-negative C33A cervical cancer cells, HPV-positive SCC152 (HPV16) and HPV-negative FaDu head-and-neck cancer cells, and human foreskin fibroblasts (HFF) were all from the American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Migration, Transformation Assay, Concentration Assay, Inverted Microscopy, Incubation

Analysis of the effect of the drug combination on HPV-positive cervical and head-and-neck cancer cells viability.

Journal: Cancers

Article Title: Targeted Disruption of E6/p53 Binding Exerts Broad Activity and Synergism with Paclitaxel and Topotecan against HPV-Transformed Cancer Cells

doi: 10.3390/cancers14010193

Figure Lengend Snippet: Analysis of the effect of the drug combination on HPV-positive cervical and head-and-neck cancer cells viability.

Article Snippet: HPV-positive HeLa (HPV18), CaSki (HPV16), SiHa (HPV16), ME180 (HPV68), MS751 (HPV45), and HPV-negative C33A cervical cancer cells, HPV-positive SCC152 (HPV16) and HPV-negative FaDu head-and-neck cancer cells, and human foreskin fibroblasts (HFF) were all from the American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: