Answer:
Explanation:
cystic fibrosis is an autosomal recessive disorder. When the child receives the defective gene from both of his parents, he suffers from cystic fibrosis. Because his parents are carriers. In recessive genetic disorder, the genes will be expressed when both recessive genes are present in one person. The person suffering from this disease have a lung infection and pancreatic dysfunction.
In this cystic fibrosis, genes are located in chromosome 7. The effective gene is the CFTR gene. The CFTR gene is present in the DNA and by transcription, this forms CFTR protein. This is a channel protein and transports chloride ion.
This CFTR protein transports chloride ions and it makes a balance in the cell membrane. These genes are commonly present in the epithelial cells. Outside the epithelial mucus is present to keep the cells moist.
The epithelium gets a lack of water and chloride due to the defect. Therefore cells need CFTR proteins also. This causes lung infection and pancreatic disorder.
Hello. You forgot to mention that this question is about the poem "Icarus's Flight". it is necessary that you always provide all the necessary information for your question to be answered as you deserve.
Answer:
The poem states that Icarus did the right thing because he used his skills to try to achieve his desire, instead of just wondering if "would it have worked?"
Explanation:
In short, we can say that the poem states that Icarus did the right thing, because he allowed himself to try. He had a desire, which he knew was risky, but he preferred to use his skills, rather than just theorizing about what might or might not happen. Icarus had a desire and he challenged himself and went after it, instead of just whining and questioning.
The poem shows, in the eighteenth line, that even in the face of possible failure, Icarus' experience would allow him to know himself better, knowing his weaknesses and strengths.
Answer:One EcoRI site can be found in 4096 bp.As EcoRI can not cut a sequence if it is not complete, so 732421 recognition sites in human genome can be found. As you know human genome is linear genome, and when you digest it with Restriction Endonuclease having one recognition site, it always gives two fragments.
Explanation: (Idek how to explain it tbh..sorry :C )
D. 99% of all living things that have ever existed are now extinct
The scenario will be Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son
<h3>What is color blindness?</h3>
The condition is frequently inherited. Certain eye diseases and medications are also possible causes. Men are more affected than women.
Color blindness is characterized by the inability to distinguish between red and green shades.
A colorblind man's genotype is XcY, and a heterozygous carrier female's genotype is XcX. A cross between XcY and XcX would result in progeny with the following ratio=
Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son.
Thus, the couple is likely to have a son who is half normal and half affected. Similarly, the couple is likely to have 50% normal daughters and 50% colorblind daughters.
For more details regarding color blindness, visit:
brainly.com/question/25621649
#SPJ1
