For B. It is CAC
For the rest there needs to be a codon table for us to see
A parent with one non-functional copy of the gene is a carrier. Carriers for Cystic fibrosis will have no symptoms but they can pass the non-functioning gene on to their children.
<h3>What is cystic fibrosis?</h3>
Cystic fibrosis is a genetic disease and individual must inherit two non-functioning CF genes that is one from each parent to have CF. Both parents must have at least one copy of the defective gene and people who have only one copy of the defective CF gene are called carriers but they do not have the disease. Many couples who have a child with CF have no family history of cystic fibrosis
Cystic fibrosis affects cells that produce mucus, sweat, and digestive juices and also it causes these fluids to become thick and sticky. They block tubes, ducts, and passageways.
Symptoms include cough, repeated lung infections, inability to gain weight, and fatty stools. Treatments for this disease may ease symptoms and reduce complications.
To know more about cystic fibrosis, refer
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Answer:
To turn sugars into energy
Explanation:
- Mitochondria are main sites of aerobic respiration. They are miniature biochemical factories where food stuffs are completely oxidised to carbon dioxide and water.
- The energy (ATP) produced in the mitochondria helps to perform various energy requiring processes.
- Because of the formation of ATP in mitochondria it is called power house of the cell.
- Photosynthesis: Light reaction (in thylakoids), Dark reaction (in stroma).
- Storage of starch.
Phospholipid is the answer
