How to Perform Rate Asymmetry in Genomes
Things You'll Need
- Human fibroblast cell lines
- Maintenance medium
- Gamma and UV radiation source
- Centrifuge
- Incubator
- Phosphate-buffered saline
Instructions
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Incubate the human fibroblast cell lines in a medium containing chemicals such as thymidine, penicillin, glutamine and fetal bovine serum at 37 degrees Fahrenheit in an incubator chamber with 5 percent carbon dioxide.
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Expose the cell lines to light sources with gamma and ultraviolet radiation for 30 minutes. Place the cell lines back in the incubator for 18 to 24 hours.
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3
Make suspensions of the cell cultures in fresh growth medium and incubate again for one or two hours in the incubator.
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4
Use the alkaline sucrose sedimentation method to study the stability and structure of the DNA. Dilute the cells in 20 volumes of phosphate-buffered saline and centrifuge at 1,000 revolutions per minute for four minutes at an angle of 4 degrees. Mix the solution with sodium hydroxide and sodium chloride, then identify the DNA growth phase and structure for any changes.
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