The two strands of DNA are held together by hydrogen bonds. Heat causes disruption of these bonds and therefore separation of the strands. This separation is called denaturation, or, rather strangely, melting. It has nothing to do with normal melting.
Boiling can allow for the extraction of DNA.
This step is used to danature DNA (separate two strands) by NaOH: Denature the DNA by adding freshly prepared NaOH (3 M) to a final concentration of 0.3 M. Incubate at 42°C for 30 min.
No, DNA is not soluble in ethanol. When the 2 are mixed, DNA can be spooled out by stirring the solution with a glass rod.
Native DNA precipitates as fibers when alcohol is added to a solution containing DNA. The DNA fibers can then be spooled onto a glass rod.
To precipitate the DNA out of solution. It is usually done in the presence of salt, such as sodium chloride or potassium sulfate. This process is called "salting out", meaning becoming out of solution (water), which also can be done with other electrically charged molecules (ionized), including proteins.
To denature the DNA
Not directly. Radiation can cause mutations in DNA. Excess heat (as in the case of a fever) can denature (destroy) the DNA sequence as well as other proteins which will usually result in cell death.
To denature DNA
Through the magic of hydrogen bonding
In the PCR, high temperatures are used in order to separate both strands of DNA readily. Normal DNA polymerases would "melt" (denature) under these conditions, whereas Taq DNA Polymerase does not (short from Thermus aquaticus, a bacteria that lives in very hot submarine springs).
Unlike Taq DNA polymerase, E.coli DNA polymerase is not heat-stable and will denature during the strand denaturation step of the PCR reaction.
by heating above certain temprature eg.90 or 100 degree celcius or by treting with strong alkali or strong acid you can denature your DNA *Actually, you can denature DNA in water if you wanted to. Basically any polar solvent will denature DNA because it has a negatively charged sugar-phosphate backbone. Mutagens can also influence DNA although it isn't exactly denaturing it. So can high energy light, like UV or all kinds of radiation. This, too, isn't denaturing though.
Simply put, heat will denature DNA. Technically speaking, DNA has something known as the the melting temperature (which is the temperature at which a strand of DNA is separated halfway). And melting temperature is itself dependent on several other factors (like G to C ratio, salt conent, and pH).
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.
DNA does not dissolve on Alcohols. It is better to store it in cold temp. for it not to denature
Chelex is there to simply denature the Double stranded DNA and convert it to single strand DNA so the primers can attatch to it during PCR.
Boiling can allow for the extraction of DNA.