How Does Comet Assay Work at Simon Cho blog

How Does Comet Assay Work. The comet assay is a versatile method for measuring dna strand breaks in individual cells. The comet assay (single cell gel electrophoresis) is the most common method for measuring dna damage in eukaryotic cells or disaggregated. It can also be applied to cells isolated from treated. Simply put, the amount of dna which leaves the nucleus is a measure of the amount of dna damage to the cell. The brighter and longer the dna tail, the higher the level of damage. The comet assay is used to follow the accumulation of dna breaks (repair intermediates) with time of incubation.

Representative images of comet assay and percentage damage Download
from www.researchgate.net

The brighter and longer the dna tail, the higher the level of damage. It can also be applied to cells isolated from treated. The comet assay is used to follow the accumulation of dna breaks (repair intermediates) with time of incubation. Simply put, the amount of dna which leaves the nucleus is a measure of the amount of dna damage to the cell. The comet assay (single cell gel electrophoresis) is the most common method for measuring dna damage in eukaryotic cells or disaggregated. The comet assay is a versatile method for measuring dna strand breaks in individual cells.

Representative images of comet assay and percentage damage Download

How Does Comet Assay Work The comet assay (single cell gel electrophoresis) is the most common method for measuring dna damage in eukaryotic cells or disaggregated. Simply put, the amount of dna which leaves the nucleus is a measure of the amount of dna damage to the cell. It can also be applied to cells isolated from treated. The comet assay is used to follow the accumulation of dna breaks (repair intermediates) with time of incubation. The brighter and longer the dna tail, the higher the level of damage. The comet assay is a versatile method for measuring dna strand breaks in individual cells. The comet assay (single cell gel electrophoresis) is the most common method for measuring dna damage in eukaryotic cells or disaggregated.

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