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The frist part of DNA isolation involves separating the nucleic acids from other cellular components. A centrifuge is required to partition proteins from the nucleic acids
Its a centrifuge.
Phosphate Buffered Saline (PBS): a salty solution of constant pH to keep tissues, cells, and proteins intact during maceration
PCR
Its purpose is to isolate DNA from a protein mixture.
DNA is not soluble in isopropyl alcohol. It will precipitate out when you add this solvent. Once out of solution you can centrifuge it down and collect the pellet of DNA.
The frist part of DNA isolation involves separating the nucleic acids from other cellular components. A centrifuge is required to partition proteins from the nucleic acids
The two strands can not be separated mechanically.
Its a centrifuge.
Phosphate Buffered Saline (PBS): a salty solution of constant pH to keep tissues, cells, and proteins intact during maceration
PCR
Its purpose is to isolate DNA from a protein mixture.
To produce enough copies of a DNA sample, that identification can be made of the source of the DNA sample.
Supernatant liquid is the upper layer of fluid found after a mixture has been centrifuged. Because of its lower density, the fluid and the components in it have a lesser tendency to migrate to the bottom of a centrifuge tube.
Which of the DNA typing techniques do you think you would choose if you had to analyze a DNA sample? Why?
Sodium chloride was needed to ensure the proteins in the cell aren't separated from the rest of the solution with the DNA.
mitochondrial sample