Photosynthesis is
6 CO2 + 6H2O---> C6H12O6 + 6 O2. So unless I understand the question wrong, none is needed to do, but glucose and oxygen are products after the photosynthesis
Answer:
I think it would be B: Our brains add details and general knowledge to childhood memories.
Sorry if its not correct
Explanation:
Answer:
mRNA must start membrane protein in the cytoplasm and, after that, continue it in the rough ER.
Explanation:
Protein synthesis is initiated when mRNA meets a free ribosome, the primary structure for protein synthesis. Ribosomes can be found in the r<em>ough endoplasmic reticulum</em> or floating in the cytosol. They read the mRNA code and add the correct amino acid using transference RNA to build the protein.
The <u>rough endoplasmic reticulum</u> is in charge of the synthesis and transport of the membrane proteins. It is also in charge of the latest protein modifications after transduction. Synthesis of membrane proteins <u>starts in the cytoplasm</u> with the production of a molecule portion known as a signal sequence. This portion leads the synthesizing protein and associated ribosome to a specific region in the Rough endoplasmic reticulum where it continues the protein building.
Membrane proteins are synthesized in the endoplasmic reticulum and <em>sent to the Golgi complex in vesicles</em>, where it happens the final association of carbohydrates with proteins. Finally, protein is transported <em>from the Golgi complex to its final destiny, the membrane. </em>
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.
Answer:
The correct answer would be - Characteristics can be lost in evolution.
Explanation:
The new evidence helps in developing a new hypothesis. In this case, new evidence proved that the Chondrichthyes diverged after the evolution of bone had started instead of before the evolution started. This process called atavism where an ancestral genetic trait reappears after having lost. This leads to loss of the traits in the evolution
This can take place by knocking the mutation out to overriding the gene by the old gene or overriding the new trait by the old trait during the evolution period.
