Answer:
I am assuming that the mutant cells have mutated beta galactosidase activity hence the relative levels of enzymatic activity would be reduced.
Answer:
The options are
a.cooling of the power plant
b.mining of uranium
c.storage of radioactive waste
d.monitoring the reactor
The answer is b.mining of uranium
Explanation:
Uranium is known as a radioactive element which is used as a fuel to power a nuclear energy plant. Mining of uranium could cause it to mix with air and water which results in contamination.
When contamination occurs and it gets into the body of humans or animals by inhalation or ingestion it poses a high risk of cancer and kidney damage.
DNA helicase is the enzyme that unwinds the DNA double helix by breaking the hydrogen bonds down the center of the strand. It begins at a site called the origin of replication, and it creates a replication fork by separating the two sides of the parental DNA.
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Please give brainliest!
Answer:
The answer is 50
Explanation:
Hemophilia is a X-linked disease. That means the recesive allele which causes the disease is not in Y chromosome, but only in X chromosome. If we denote:
X⁺ : dominant allele
X⁻: recesive allele
Then, in a woman there are three posibilities:
X⁺X⁻: is a carrier woman (without hemophilia)
X⁺X⁺: healthy woman
X⁻X⁻: woman with hemophilia
But in a man there are two posibilities:
X⁺Y: healthy man
X⁻Y: man with hemophilia
A man with hemophilia is X⁻Y, and a healthy woman whose mother had hemophilia is a carrier woman (X⁺X⁻). If they have a child, there are 4 posibilities, and each one has 1/4 of occurrence probability:
X⁻Y x X⁺X⁻ = X⁻X⁺, X⁻X⁻, X⁺Y, YX⁻
Posibilities with hemophilia are X⁻X⁻ and YX⁻ (1/4 + 1/4= 1/2= 0.5= 50%)
In each filial, there is a 50 percent of probability of having a child (man or woman) with hemophilia.
Answer:
Taxonomy allows a better understanding of relationships among species.
Explanation:
