Answer:
Hemophilia is a sex-linked recessive disorder in which a person's blood do not clots and he can bleed to death even after minor injuries because blood will keep running due to a small cut.
It is a recessive trait which means that even if one normal gene is present along with Hemophiliac gene, the person will not have the disease and he will be the carrier.
Question: What will be their children’s possible phenotypes?
If a woman who is a carrier for hemophilia marries a hemophiliac man, their genotypes can be denotes as :
Here H, indicate normal gene and small h indicate defected (hemophilia) gene.
Parents: XHXh X XhY
Offspring: XHXh : XHY: XhXh: XhY
Phenotype of offspring:
XHXh: The child will be daughter and normal (25 % chances)
XHY: The child will be son and normal (25 % chances)
XhXh: The child will be girl and Hemophiliac (25 % chances)
XhY: The child will be son and Hemophiliac (25 % chances)
Hope it helps!
Answer:
i believe that the answer is sedimentation
The right answer is B.
Insulin is a hormone naturally secreted by the pancreas, specifically by specialized cells located in the islets of Langerhans. It allows glucose (sugar) to pass blood into the cells of the body. These will use glucose as energy or store it for future use.
In healthy subjects, insulin is secreted continuously. The body produces insulin according to the needs and foods consumed. For example, after a meal, the pancreas secretes additional insulin, allowing blood glucose to stay within normal limits.
Answer:
Insulin regulates blood glucose levels
Catalyst. A catalyst is a substance that increases the rate of a reaction without being consumed the rate of a reaction without being consumed in process, or being chemically altered. There are many enzymes present in cells, proteases, lipases, that speed up metabolism, and catalysts .
hOpe this has helped you any . >)
