Answer:
b. Forward or reverse primers
Explanation:
Sanger sequencing is a technique of DNA sequencing based on the extension of DNA fragments with variable sizes terminated with dideoxynucleotides at the 3′ end. This technique was developed by Frederick Sanger in 1977. In Sanger sequencing, a short primer is added in order to bind by complementarity to the target DNA region of interest. Subsequently, a DNA polymerase adds nucleotides (A, T, C and G) in the 5'-3' direction. Finally, the extension of the DNA strand is stopped by adding dideoxynucleotides, which are nucleotide analogs (i.e., modified nucleotides) that act as DNA synthesis terminators.
Differences of chilopoda and diplopoda are above .
NADH and FADF2 are the reduced forms of the nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD) coenzymes.
<h3>What is nicotinamnde adenine dinucleotide?</h3>
The nicotinamnde adenine dinucleotide (NAD) is a coenzyme used in the transport electron chain of the cellular respiration.
The movement of electrons is coupled to a proton gradient in order to generate ATP, the energy coin of the cell.
In conclusion, NADH and FADF2 are the reduced forms of the nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD) coenzymes.
Learn more about NADH here:
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