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.
The difference is because there about different from one another, the reflexes will act different towards the speed
Answer: b - Chondroblasts within the cartilage divide and secrete new matrix
Explanation: Chondroblasts are derived from two sources; mesenchymal cells within the center of chondrification and chondrogenic cells of the inner cellular layer of the perichondrium (coverings that lie over most cartilage).
At the chondrification centers, the cartilage forming cells (Chondroblasts) begin to secrete the components of extracellular matrix of cartilage. As the amount of matrix increases, the Chondroblasts become separated from each other and they are located in small cavity within the matrix called lacunae.
Concurrently, the cells differentiate into matured cartilage cells called chondrocytes.
Calm waters <span>theory of organizational change</span>
iconic bond -> sharing of many electrons
metallic bond -> sharing of electrons
covalent -> transferring of electrons
hope this helps...
