I believe it is gel electrophoresis.
Gel electrophoresis is a techniwue used to separate DNA fragments or other macromolecules such as RNA and proteins based on their size and charge. It can also determine the actual size of a piece of DNA by examining it next to a standard "yardstick" made up of DNA fragments of known sizes.
how is bacillus pumils produce no se
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 think it brings to the warm places cold air and to cold places it brings warm air
