The first step of the energy usage for growth is the breakdown process. In order the animal cells can use the food, the food they eat must be broken down into smaller molecules. Step 2 is the process glycosis which converts each molecule of glucose<span> into two smaller molecules of Acetyl CoA. Step 3 is the complete oxydation of acetyl, CoA to H2O.</span>
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A method by which you could separate mRNA from the other types of RNA in a eukaryotic cell is oligo (dT) chromatography.
<h3>What do you mean by mRNA?</h3>
mRNA may be defined as a molecule in cells that holds codes from the DNA in the nucleus to the sites of protein synthesis in the cytoplasm.
The mRNA can be easily isolated from other types of RNA by the most reliable and convincing method of oligo (dT) chromatography which is the magnetic separation method that bounds oligo (dT) molecules on the surface of paramagnetic beads.
Therefore, a method by which you could separate mRNA from the other types of RNA in a eukaryotic cell is oligo (dT) chromatography.
To learn more about mRNA, refer to the link:
brainly.com/question/884041
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Answer:
(a) 1/2; (b) no
Explanation:
Glucose-6-phosphate dehydrogenase deficiency (G6PD) is an X-linked recessive disorder and the woman's father was diseased so it means that woman is a carrier of the allele but has normal phenotype. It means that she will have XXᵇ genotype.
In contrast to this, her husband is diseased so his genotype will be XᵇY.
The Punnett square diagram related to the cross is attached.
(a) Proportion of their sons expected to be G6PD is 1/2:
They both may give birth to 4 progeny with genotypes XXᵇ, XᵇXᵇ, XY and XᵇY. It means they both may have 2 sons out of which one with genotype XᵇY will be diseased while the one with genotype XY will be healthy. So the proportion of their sons having G6PD is 1/2 or 50%.
(b) If the husband were G6PD deficient, the answer will not change.
The reason behind this is that this disease is caused by an allele located in X chromosome. But father contributes only Y chromosome to his son not X chromosome. The X chromosome will affect the genotype of his daughter not son that is why answer will not change. It means they will still have 1/2 of their sons diseased.