It seems that you have missed the necessary options for us to answer this question so I had to look for it. Anyway, here is the answer. If one parent is homozygous for a recessive allele and one parent is heterozygous for a recessive allele in an autosomal dominant genetic disorder, the chance that <span>a child of those two parents will have the disorder is 75%. Hope this helps.</span>
Answer:
14 chromosomes
Explanation:
Each gamete will get half of the number of the original chromosomes
Solution:
People that born with hemophilia lack or have a low amount of a clotting factor.
Coagulation factors are proteins necessary for normal blood clotting.
Coagulation factors are found in blood plasma. These factors act with Thrombocytes to clot blood.
However, hemophilia is not a decrease in Thrombocytes but a decrease in coagulation factors due to genetic causes.
Diagnosis includes screening tests and clotting factor analysis. Screening tests are blood tests that show whether the blood is clotting properly. Clotting factor tests can reveal a deficiency of clotting factors in the blood plasma and determine the level of severity of hemophilia.
As the coagulation factors are in Blood plasma, we can conclude that the correct answer is:
BLOOD PLASMA
Some arteries carry oxygenated blood just as some capillaries do.
Some veins carry deoxygenated blood just like some capillaries do.
If the temperature is too low, enzyme molecules don’t have enough kinetic energy to collide and combine with other substrate molecules. So the enzyme activity/ reaction rate will be very low. The rate will rise again once the temperature increases to its optimum temperature.
But if the temperature is too high, enzyme will be denatured, which means the shape of the active site of the enzyme is changed. It can no long combine with other substrate molecules. The rate will drop significantly. Yet, lowering the temperature won’t help because denaturation is permanent and irreversible.
