Because the air freshener is being released out in to open, so it spreads everywhere.
Hope that helps :)
Genetic fingerprinting – the analysis of DNA in order to identify the individual from which the DNA was taken to establish the genetic relatedness of individuals. It is now commonly used in forensic science (for example to identify someone from a blood sample) and to determine whether individuals of endangered species in captivity have been bred or captured from the wild.
<span>•DNA sequencing – the determination of the precise sequence of nucleotides in a sample of DNA or even a whole genome e.g. the Human Genome Project. </span>
<span>The process of electrophoresis: </span>
<span>DNA is chopped, close to the VNTR regions, into fragments using restriction enzymes. The DNA fragments are placed on the agarose gel and a direct current is applied continuously to the gel. The DNA fragments are attracted to the anode. The shorter the fragment, the faster it moves. </span>
<span>The fragments are transferred onto an absorbent paper placed on top of the gel. The paper is heated to separate the 2 strands in each DNA molecule. Complementary probes which have a radioactive phosphorus isotope are and this pair up with the DNA strands. The paper is placed on an X-ray film and the film goes dark due to radiation emitted by the probes. Now we end up with a pattern of dark stripes on the film matching the positions reached by the fragments in the agarose gel.</span>
From nucleic acid to amino acid apex i think
Answer:
Enzymes are influenced by changes in pH. Enzymes are best dynamic at ideal pH. It is the most favorable pH value - where the compound is most dynamic. Above and beneath to this ideal pH influence enzyme action. Accordingly enzyme show catalytic action at ideal pH.
At the point when enzymes are st low or high pH. Hydrogen particles interface with amino corrosive present at dynamic site. In this way changes their state of amino acids, their legitimate direction and influence enzyme movement.
While estimating action of enolase . 2 phospho glyceraldehyde is a substrate for enolase included a response tube. After appropriate in hatching measure of item is estimated (PEP). Proportion of PEP to 2 phospho glyceraldehyde gives thought regarding enzyme action.
For negative control, we will take a response tube, without having any enzyme enolase in it. Along these lines we will ready to preclude any change of 2 phospho glyceraldehyde to PEP without enzyme.
All compound present in our body are adjusted to as per the earth where we are living. In this manner makes us effective in C. aurantiacus ideal temperature for enolase is 55 degrees. So this catalyst will consistently work best at 55 degrees than at 37 degree
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