Answer:
The correct answer is (C) A flexible lipid double layer. The cell membrane is often referred to as a "fluid mosaic," a flexible structure
Explanation:
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Answer:
1) By selecting the genetic information that is passed on to future generations, genetic engineering is similar to natural selection.
3) By selecting the genetic information that is passed on to future generations, genetic engineering can happen at a different rate than natural selection.
4) Like natural selection, genetic engineering may be used on all organisms, including humans.
Explanation: In natural selection there is overtime selection for one particular trait and is mostly based on phenotype, whilst genetic engineering uses genotype of an organism and it is the deliberate modification of an organism by manipulating the genetic material
The human Y chromosome is about 50 million base pairs long. One would expect to find 250,000 nucleosomes associated with this chromosome.
A nucleosome typically contains 200 base pairs. On dividing 50 million by 200, one would get 250,000 which would tell about the number of nucleosomes associated with the human Y chromosome.
A nucleosome is a segment of DNA that is wrapped around a core of proteins. A nucleosomes constitutes the repeating unit of a structure in nucleus known as chromatin (thread-like stained bodies present in nucleus).
The nucleosomes in chromatin appear as 'beads-on-string' when viewed under an electron microscope.
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Answer:
Because she raised me and my dad walked out and she has been the only person there for me in my life and she has helped me through all the struggles in my like so that’s why I love my mom!
Explanation:
Answer:
Waldemar carried the recessive allele.
Explanation:
The carrier is the individual that has the affected allele or mutation but does not express the trait, or might express it in different levels. Although, as the person carries the mutation, she or he might transmit the genetic mutation associated with a disease to the progeny. In general, these diseases are inherited as recessive traits.
So, in the exposed example we know that:
- hemophilia is a sex-linked disorder
- hemophilia is determined by a recessive allele on the X chromosome.
- Irene is a carrier.
- Her husband is not a carrier.
- Her children Waldemar and Henry have hemophilia.
If Irene is a carrier, this means that she is heterozygous and that her genotype is X⁺X⁻ (Being the symbol + the dominant allele, and - the recessive one for that expresses the trait)
The fact that Irene´s husband is not a carrier means that his genotype is X⁺Y
Their boys Waldemar and Henry have hemophilia, so both their genotypes are X⁻Y
The best evidence to prove that Irene was heterozygous for hemophilia is that Alice carried the recessive allele.
- Alice is Irene´s Mother, and she is a carrier as well. Irene´s father, Louis, is not a carrier, so she could have inherited a dominant allele from her father and a recessive allele from her mother, X⁺X⁻, or she could have inherited two dominant alleles from both her parents X⁺X⁺. This is not proof enough of Irene being heterozygous.
- The fact that Alexandra, Irene´s sister, was also a carrier does not say anything about Irene´s genotype, because they could both share the same genotype or not. This is not proof of Irene being heterozygous.
- Frederick (her brother) was hemophilic. He received a recessive allele from Alice, but this does not say anything about Irene´s genotype.
- The fact that Waldemar (her son) was hemophilic, is the best evidence to prove that Irene was heterozygous for hemophilia. Walderman received the Y chromosome from his father and an X chromosome from his mother. The X chromosome that he received from his mother carried the recessive allele for the trait, and this is why he had hemophilia. This means that there is no best evidence for Irene´s genotype than her son´s genotype.