We know that Hardy-Weinberg conditions include the following equations:

where 
And where p = dominant, and q = recessive; this means that
is equal to the homozygous dominant,
is the heterozygous, and
is the homozygous recessive .
So we have 100 total cats, with 4 having the recessive white coat color. That means we have a ratio of
or 0.04. Let that equal our
value.
So when we solve for q, we get:


Now that we have our q value, we can use the other equation to find p:



So then we can solve for our heterozygous population:

This is the ratio of the population. So we then multiply this number by 100 to get the number of cats that are heterozygous:

So now we know that there are 32 heterozygous cats in the population.
The chemical formula would be
CTGA or any of the combinations of the four nitrogenous bases
The nucleotide is made up of four bases which makes it a tetranucleotide and the arrangement of each bases create a linear geometry.
Answer: The mother of the man can be either XHXH or XHXh and pass her normal allele to the son and his father can be either XHY or XhY, he only passes his Y chromosome. The mother of the woman can be XHXH or XHXh and the father could be XhY, then she could have inherited the normal allele from the mother and the affected allele from the father. But also, the mother of the woman could be XHXh or XhXh and the father could be XHY, so in this case she could have inherited the normal alele from the father and the affected allele from the mother.
Explanation:
Hemophilia is an inherited bleeding disorder in which the blood does not clot properly. This can cause bleeding either spontaneously or after an injury.
<u>It is related to the X chromosome and it is recessive for females</u>, this mean they need both affected alleles to develop the trait. <u>Males only need one recessive allele because they only have one X chromosome</u>. This means that females need both parents to be at least carriers (although one or both can also have the disease or both recessive alleles). While males inherit it only from the mother, either she is a carrier (one recessive allele) or she has the disease (both recessive alleles). Then the mother passes the X chromosome with the affected allele to the son, and that son only receives the Y chromosome from the father, which does not have the gene that determines this disease.
If the mother is a carrier, her genotype is XHXh, being XH the normal allele and Xh the affected allele. She does not have hemophilia because she has a dominant allele. The father is XHY, so he does not have the disease because his only allele is normal (dominant)
The mother of the man can be either XHXH (she can only pass a normal allele) or XHXh and pass her normal allele to the son (in this case, the recessive allele is not inherited by chance.) His father can be either XHY or XhY, he only passes his Y chromosome which is not related to the disease. The mother of the woman can be XHXH or XHXh and the father could be XhY, then she could have inherited the normal allele from the mother and the affected allele from the father. But also, the mother of the woman could be XHXh or XhXh and the father could be XHY, so in this case she could have inherited the normal alele from the father and the affected allele from the mother.
Answer:
NAD is a coenzyme found in all cells. It consists of two nucleotides linked through their phosphate groups with a nucleotide that contains an adenosine ring and another that contains nicotinamide.
Explanation:
In metabolism, NAD participates in oxidation reduction reactions. This coenzyme is found in two forms in the cells: NAD and NADH. NAD accepts electrons from other molecules and is reduced, forming NADH, which you can use as a reducing agent to donate electrons. These electron transfer reactions are the main function of the NAD.
In living organisms, NAD can be synthesized from scratch from the amino acids tryptophan or aspartic acid. Some NADs are found in nicotinamide adenine dinucleotide phosphate (NADP), whose chemistry is similar to NAD, although it has different functions in metabolism.