Resuspension buffer (solution I) is used for the isolation of plasmid DNA by alkaline lysis method. Bacterial cells, obtained from the culture (liquid culture or colonies grown on agar plate), is resuspended in this buffer. The purpose of this buffer is to provide an optimal starting pH (pH 8.0) and an ideal condition for subsequent lysis.
Agarose is not used in DNA isolation. Agarose is used to prepare a gel in which DNA fragments can be separated based on size
LB medium
Several DNA isolation protocols recommend the use of either ethyl or isoamyl alcohol for the precipitation step
it is SDS like detergent added at to lyse cells
CTAB is a detergent used to denature proteins from samples. Once the protens have been denatures, the isolation of DNA from the non required waste materials can begin.
Good morning, the TEG contains TRIS to keep pH of solution constant, EDTA to capture ions Ca2+ and Mg2+ in solution (which may interfere in the isolation of DNA) and Glicose/Dextrose (+- 50 mM) is used to increase the osmolarity of solution and lysin the cell. the cell swells to bursting and the DNA remains in solution.
Agarose is not used in DNA isolation. Agarose is used to prepare a gel in which DNA fragments can be separated based on size
DNA isolation is a based on the principle of purification. DNA samples are isolated through the use of physical and chemical methods. Friedrich Miescher conducted the first isolation of DNA in 1869.
DNA is soluble in chloroform more than water. So we use it.
LB medium
helps in DNA ppt
Several DNA isolation protocols recommend the use of either ethyl or isoamyl alcohol for the precipitation step
Ethanol is used to precipitate the DNA. I.e. to bring the DNA out of solution. Precipitated DNA is then spun down and re suspended in the appropriate buffer that is suitable for sample storage
it is SDS like detergent added at to lyse cells
CTAB is a detergent used to denature proteins from samples. Once the protens have been denatures, the isolation of DNA from the non required waste materials can begin.
phenol,chloroform,isoamyl alcohol,ethanol,CTAB reagent,Na acetate etc.. but nowadays, they use kits for any kind of DNA isolation, which makes their job easier.
One can rinse the mouth with a solution and the solution is put back into the tube and add the required solution to it, then you will be able see a murky/jelly-white substances on the surface of the water, and that is the DNA which was extracted from your mouth.