Recombinant DNA is a type of artificial DNA which have genes that are taken from different organisms. During this process, a gene is take from one organism and putting the gene into another organism. Basically, the technology follows cut and paste scheme to form the new brand of DNA.
So to conclude this the technology cuts part of the DNA out to create a new DNA so you are cutting and pasting new DNA which is incredible.
Hope this helped.
Answer:
The answer to your question is: D. Binary fission
Explanation:
A. Mitosis This is the process by which somatic cell divide, from 1 cell the result is 2 cells.
B. Meiosis This is process by which reproductive cells divide, the product of this process is 4 daughter cells.
C. Conjugation is a process by which bacteria transfer DNA to another cell but is not a process of division.
D. Binary fission , this is the process by which Bacteria reproduce, the result of the mechanism is 2 identical daughter cells.
Answer:
The three main steps of PCR amplification are :
Denaturation
Annealing
Elongation
Explanation:
Polymerase Chain Reaction (PCR) can best be describes as a procedure to amplify or make copies of DNA fragments.
The basic steps involved for PCR are :
1. Denaturation
In this step, the two complementary strands of DNA are seperated by the usage of heat. The best temperature for this procedure is 95°C.
2. Annealing
After denaturation, each strand of DNA serves as a template foe building a new strand. During the process of annealing, the temperature is reduced so that the primers can attach to the DNA strands. The optimum for this depends on the nature of the primers but usually the most feasible temperature is 55°C.
3. Elongation
In this step, the DNA polymerase adds nucleotides to the primers attached to the templates. The optimum temperature For DNA polymerase to work is 72°C.
I wanna say it is <span>C.) fossilization </span>