0
Spooling out precipitated DNA is challenging because the DNA strands are often entangled and can be difficult to separate from the surrounding alcohol (usually ethanol or isopropanol) used in the precipitation process. Additionally, the viscosity of the precipitated mass can make it hard to manipulate without breaking the DNA strands. Moreover, if not enough salt is present, the DNA may not aggregate sufficiently to form a cohesive mass that can be spooled effectively.
What else can I help you with?
Why pcr products are precipitated before sequencing?
The PCR product are precipitated before sequencing to increase the concentration of tamplet DNA.
Can weak acids be precipitated from solutions of their salts by lowering the pH?
Yes this may be possible.
What is the role of proteins in allowing DNA to fit in a cell?
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.
Is it possible to do legal DNA testings in hospital?
Depending on where you live it is possible to do legal DNA testing in hospitals. In the USA it is legal. In Canada most hospitals do not perform DNA testing for paternity testing.
Why do you need to break down the membrane during DNA extraction?
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.
Why pcr products are precipitated before sequencing?
The PCR product are precipitated before sequencing to increase the concentration of tamplet DNA.
The proteins in the chromosomes provide spool-like support on which DNA is wound These structures are called?
nucleosomes
A portion of a DNA molecules wound around a spool of histone proyein is called?
cell cycle
Would chromosomal DNA spool if it was heated to 100 degrees?
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.
A portion of a DNA molecule wound around a spool of histone protein is called a?
Such a structure is called a Nucleosome
What is the purpose of alcohol when extracting DNA?
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)....
Can weak acids be precipitated from solutions of their salts by lowering the pH?
Yes this may be possible.
Can weak bases be precipitated from solutions of their salts by increasing the pH?
Yes this may be possible.
Is DNA soluble in ethanol?
DNA is not soluble in ethanol alone, but it can be precipitated out of solution by adding ethanol to a DNA-containing solution. This is often used in laboratory procedures to isolate DNA from other cellular components.
What is histon?
A Histone Core is a group of Histone Proteins, mainly used in eukaryotes to package DNA strands into Nucleosomes. (Think of it like a spool for the DNA to wrap around, to be easily stored on a shelf)
Is it possible for DNA to crossover?
no its not possible
What is a spool pin?
Spool pins are used on sewing machines to hold the spool of thread. Most or vertical, some that are horizontal use a spool cap to secure the spool of thread. Some machine come with spool nets to cover the spool to ensure the thread enter the machine evenly. Some machines come with an extra spool pin that fits into a small hole on the top of the machine to hold a second spool of thread.
