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cck 8 solution vazyme  (Vazyme Biotech Co)
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Vazyme Biotech Co cck 8 solution vazyme
Cck 8 Solution Vazyme, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cck 8 solution vazyme/product/Vazyme Biotech Co
Average 99 stars, based on 1 article reviews
cck 8 solution vazyme - by Bioz Stars, 2026-02
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cck-8 solution  (NovoPro Biosciences Inc)
90
NovoPro Biosciences Inc cck-8 solution
( A ): EdU staining was used to detect the proliferative ability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out (200× magnification). ( B ): Bar graph showing the results of EdU staining for the proliferative ability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out. The ratio (%) was calculated as the number of Apollo643-stained cells divided by the number of Hoechst33342-stained cells. In comparison to the control group, there was no significant difference in the proliferative activity of the experimental group cells. ( C ): The <t>CCK-8</t> assay was used to measure the viability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out. The proliferative activity of the experimental group cells, compared to the control group, showed no significant difference.
Cck 8 Solution, supplied by NovoPro Biosciences Inc, 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/cck-8 solution/product/NovoPro Biosciences Inc
Average 90 stars, based on 1 article reviews
cck-8 solution - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

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( A ): EdU staining was used to detect the proliferative ability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out (200× magnification). ( B ): Bar graph showing the results of EdU staining for the proliferative ability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out. The ratio (%) was calculated as the number of Apollo643-stained cells divided by the number of Hoechst33342-stained cells. In comparison to the control group, there was no significant difference in the proliferative activity of the experimental group cells. ( C ): The CCK-8 assay was used to measure the viability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out. The proliferative activity of the experimental group cells, compared to the control group, showed no significant difference.

Journal: Genes

Article Title: Identification of Two Potential Gene Insertion Sites for Gene Editing on the Chicken Z/W Chromosomes

doi: 10.3390/genes15070962

Figure Lengend Snippet: ( A ): EdU staining was used to detect the proliferative ability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out (200× magnification). ( B ): Bar graph showing the results of EdU staining for the proliferative ability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out. The ratio (%) was calculated as the number of Apollo643-stained cells divided by the number of Hoechst33342-stained cells. In comparison to the control group, there was no significant difference in the proliferative activity of the experimental group cells. ( C ): The CCK-8 assay was used to measure the viability of DF-1 cells with EE0.6 and NC_006127.4 loci knocked out. The proliferative activity of the experimental group cells, compared to the control group, showed no significant difference.

Article Snippet: The cells were pre-cultured for 24 h before adding 10 μL of CCK-8 Solution (A311-01, NovoPro, Shanghai, China) to each well.

Techniques: Staining, Comparison, Control, Activity Assay, CCK-8 Assay