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The PCR product are precipitated before sequencing to increase the concentration of tamplet DNA.
Yes this may be possible.
Yes it is possible to isolate DNA from bone.
The DNA is present inside the cell and the cell is encapsulated by the plasma membrane. In, eukaryotes, the DNA is further localized in the nucleus and that is also surrounded my nuclear membrane. If one would not rupture the membranes, the DNA will not come in the solution and could not be precipitated.
The protein histone, and attendant proteins, spool the DNA tightly around their complexes and then further wind these complexes into tighter and tighter shapes. About two meters worth of DNA per cell is held in these histone complexes.
The PCR product are precipitated before sequencing to increase the concentration of tamplet DNA.
Detergent denatures (breaks up) proteins, which can then be precipitated and the DNA can be isolated
In the process of DNA isolation, ethanol is used to preciputate the DNA or bring the DNA out of solution. Once precipitated, DNA appears as a white cottony mass that can be seen with the naked eye. This precipitated DNA is then spun down and re suspended in the appropriate buffer suitable for storage.
nucleosomes
cell cycle
If heated to a hundred degrees, chromosomal DNA would denature. Meaning the it would come apart and the complementary DNA strands would separate. One way to get DNA to spool (around a glass rod for example) is to remove it from the cell and precipitate it in solution. This can be done with with help of sodium chloride and isoamyl alcohol.
Such a structure is called a Nucleosome
dna has a comparatively long structure
According to me, we use alcohol because DNA is insoluble in alcohol, it aggregates together, giving a pellet in centrifugal and we can see a precipitated DNA with naked eyes (that we suppose to see in experiment i.e DNA extraction)....
Yes this may be possible.
Yes this may be possible.
1.2mm mig weighs 0.0087kg/meter therefore 1.724km per 15kg spool