Answer:
G-banding or Giemsa banding is a technique used to study the chromosomes by staining then at condensed stage. The visible karyotype can be used by this technique. The genetic diseases can be easily identified by this G banding technique.
The base composition of the genes (nucleotide) are stained by the dye known as Giemsa stain. The nitrogenous base adenine and thymine of the heterochromatic region of chromosome stained darkly in this technique. The darkly stained area is generally gene poor area.
Answer:
The answer is 25%.
Explanation:
Hemophilia is a recessive illness that is x-linked.
If the husband has normal clotting ability, that means he has the dominant gene since he has only one X chromosome.
Since there is a probability that their child will have hemophilia, this means that the woman, who has 2 X chromosomes but has normal blood clotting abilities, has one dominant and one recessive hemophilia gene.
The probability that their first child will be a male is 50% and the probability that he will have hemophilia is also 50% since he will only get the Y chromosome from the father and the mother has one dominant and one recessive.
So the probability that their first child will be a son with hemophilia is 25%.
I hope this answer helps.
Answer:
They are ATP and ADP. ....
Became increasingly greek
Answer:
True
Explanation:
The arteries (red) carry oxygen and nutrients away from your heart, to your body's tissues. The veins (blue) take oxygen-poor blood back to the heart. Arteries begin with the aorta, the large artery leaving the heart. They carry oxygen-rich blood away from the heart to all of the body's tissues.
I hope this was helpfull
