The two pigments are chlorophyll A and B
Answer:
Changes in allele frequencies over time can indicate that genetic drift is occurring or that new mutations have been introduced into the population.
Answer:
An antisense sequence with complementary to the target mRNA encoded by the gene of interest
Explanation:
An antisense sequence is usually a short RNA sequence specifically designed in the laboratory to bind by complementary to the DNA/RNA sequence of interest (usually a target mRNA) whose expression is desired to be inhibited. When an antisense bind to its target mRNA, the antisense sequence acts to block translation, thereby inhibiting protein synthesis. Moreover, it has been shown that the double-stranded antisense-RNA complexes may also increase the susceptibility of the target sequence to RNase H digestion.
Answer:
(e)
Explanation:
Transmembrane protein are proteins that are firmly associated with membranes because it is integrated along the length of bilayer lipid membrane. This kind of protein is made up of two kinds of amino acid, hydrophilic or polar amino acid and hydrophobic or non polar amino acid. while peripheral protein loosely associated with membrane, they are present on the surface which means they are not integrated in to the cell membrane and facing intercellular fluid. this is why it contains only hydrophilic amino acid.
The primary amino acid sequence contains hydrophobic amino acid which identifies the protein as transmembrane protein. These amino acid are methionine (Met), leucine(Leu), valine(Val), glycine(Gly), tryptophan(Trp), isoleucine(Ile), phenylalanine(Phe), proline(Pro) and alanine(Ala)
These three factors affect how variations in genotype arise in a population:
<span>1) Sexual recombination- one-half of the parent 1 and one-half of parent 2’s genes are combined to form a brand new gene for the offspring resulting to a new type of combination that is not existing before.
2) Gene crossover- this is the trade-in of genetic material from two cells that each contains a pair or 1 maternal strand and 1 paternal strand of the parents chromosomes (Homologous).
</span>3) Chromosome aberration- it is a mutation in the chromosome wherein there is an extra or missing part of the DNA. <span> </span>
