Answer:
Explanat}
there is long term storage for nuclear waste
Caliceal
Pertaining to a calyx (cup-shaped collecting chamber in the central portion of the kidney).
The mass of an atom is contained primarily in its NUCLEUS.
An atom is made up of three sub particles, which are proton, neutrons and electrons. The proton and the neutrons are located in the nucleus of the atom while the electron are located outside the nucleus where they move about in continuous motion around the nucleus. The proton and the neutrons, which are located in the nucleus have the same relative mass of 1, which has been estimated to be about 2,000 times bigger than that of the electron, which has a relative mass of 0.0005. This shows that, the mass of an atom is located primarily in its nucleus. <span />
Answer:
Hydrogen bonding
Explanation:
The newly synthesised proteins as a result of the process of translation are linear structures formed by linear arrangement of amino acids.
The linear structure of a protein is known as the primary structure which changes its conformation and take the shape of either the helix or the pleated sheet. This helical or pleated sheet structure is known as a secondary structure.
The secondary structure is formed due to the bond formed between the hydrogen of the carbonyl group and the amino group which form the backbone of the protein structure. The hydrogen bond causes the linear polypeptide to form spiral helical or bend pleated sheet.
Thus, Hydrogen bonding is the correct answer.
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.
