cck 8 cell proliferation toxicity test kit Search Results


cck-8 proliferation toxicity test kit ck04  (Dojindo Labs)
90
Dojindo Labs cck-8 proliferation toxicity test kit ck04
Cck 8 Proliferation Toxicity Test Kit Ck04, supplied by Dojindo Labs, 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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cell cck 8 proliferation toxicity test kit  (Boster Bio)
96
Boster Bio cell cck 8 proliferation toxicity test kit
Cell Cck 8 Proliferation Toxicity Test Kit, supplied by Boster Bio, 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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cell cck 8 proliferation toxicity test kit - by Bioz Stars, 2026-02
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cell toxicity  (Dojindo Labs)
99
Dojindo Labs cell toxicity
Cell Toxicity, supplied by Dojindo Labs, 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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cell counting kit-8 (cck-8  (Millipore)
90
Millipore cell counting kit-8 (cck-8
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cell Counting Kit 8 (Cck 8, supplied by Millipore, 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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cck-8 kit (cell proliferation and toxicity test kit)  (Beijing Solarbio Science)
90
Beijing Solarbio Science cck-8 kit (cell proliferation and toxicity test kit)
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cck 8 Kit (Cell Proliferation And Toxicity Test Kit), supplied by Beijing Solarbio 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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cck-8 kit (cell proliferation and toxicity test kit) - by Bioz Stars, 2026-02
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cell proliferation toxicity assay kit (cck-8 method, d3100l4054)  (Dojindo Labs)
90
Dojindo Labs cell proliferation toxicity assay kit (cck-8 method, d3100l4054)
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cell Proliferation Toxicity Assay Kit (Cck 8 Method, D3100l4054), supplied by Dojindo Labs, 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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rna-out total rna extraction kit  (Nanjing Jiancheng Bioengineering Research Institute Co Ltd)
90
Nanjing Jiancheng Bioengineering Research Institute Co Ltd rna-out total rna extraction kit
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Rna Out Total Rna Extraction Kit, supplied by Nanjing Jiancheng Bioengineering Research Institute 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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cell counting kit cck-8  (Beyotime)
90
Beyotime cell counting kit cck-8
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cell Counting Kit Cck 8, supplied by Beyotime, 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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cck-8 cell proliferation toxicity assay kit  (Applygen Technologies)
90
Applygen Technologies cck-8 cell proliferation toxicity assay kit
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cck 8 Cell Proliferation Toxicity Assay Kit, supplied by Applygen Technologies, 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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cck 8  (Abcam)
96
Abcam cck 8
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cck 8, supplied by Abcam, 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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fermentation broth cytotoxicity  (TargetMol)
96
TargetMol fermentation broth cytotoxicity
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Fermentation Broth Cytotoxicity, supplied by TargetMol, 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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cell counting kit (cck-8  (Yeasen Biotechnology)
90
Yeasen Biotechnology cell counting kit (cck-8
MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting <t>kit-8</t> <t>(CCK-8).</t> Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.
Cell Counting Kit (Cck 8, supplied by Yeasen Biotechnology, 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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cell counting kit (cck-8 - by Bioz Stars, 2026-02
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Image Search Results


MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting kit-8 (CCK-8). Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.

Journal: Journal of Virology

Article Title: Merkel Cell Polyomavirus Small Tumor Antigen Activates Matrix Metallopeptidase-9 Gene Expression for Cell Migration and Invasion

doi: 10.1128/JVI.00786-20

Figure Lengend Snippet: MMP-9 inhibition impedes MCV sT-induced cell migration. (A) MCV sT promotes MMP-9-induced cell migration. Scratch assay. Poly-l-lysine-coated 6-well plates were seeded with U2OS cells and incubated with specific MMP-9 inhibitors at predetermined concentrations. Cells were transfected with a vector control, sTWT, or sTLSDm plasmids. After 48 h, a scratch was created, and migration of cells toward the scratch was observed over a 24-h period. The size of the wound was measured at 0 and 24 h and presented as the fold change in panel B. Scratch assays were performed in triplicate. (C) MMP-9 is required for MCC migration. MCV-positive MCC cell lines, MKL-1 and MS-1, were incubated with DMSO or the MMP-9 inhibitors as follows: 9-I (0.2 μM) and 9-II (2 μM) for MKL-1 and 9-I (0.1 μM) and 9-II (1 μM) for MS-1. Cells were then transferred into transwell inserts and allowed to migrate for 48 h. Migrated cells were measured using cell counting kit-8 (CCK-8). Data were analyzed using three biological replicates per experiment (n = 3). Differences between means (P value) were analyzed using a t test with GraphPad Prism software.

Article Snippet: Cell toxicity was measured using a cell counting kit-8 (CCK-8) (Sigma-Aldrich) according to the manufacturer’s protocol.

Techniques: Inhibition, Migration, Wound Healing Assay, Incubation, Transfection, Plasmid Preparation, Cell Counting, CCK-8 Assay, Software