The answer for this question is C.
<u>Answer</u>: Cystic fibrosis is a genetic disorder that causes thick mucus secretions.
<u>Explanation</u>:
- <em>Cystic fibrosis</em> is a genetic disorder caused by mutations in a gene that makes a protein called CFTR (cystic fibrosis transmembrane regulator).
- The CFTR protein normally functions as a channel for transport of chloride ions in cells responsible for mucus production.
- A person suffering from cystic fibrosis produces abnormal CFTR protein or no CFTR protein at all.
- This is the reason that thick, sticky mucus is produced instead of the thin, watery kind.
The answer is; endocytosis
This is a form of active transport that enable cells to import large particles that cannot pass across the membrane. It is a bulk transport system. The opposite of endocytosis s exocytosis where the cell expels large particles to the outside of the cell.
Proteins are polymers of amino acids. There are a fixed set of amino acids that are involved in the making of a protein. These amino acids are varied in number and type to give rise to different combinations in a polymer. This creates a diversity of protein molecules.
The amino acids link to other amino acid in the polymer through the formation of a peptide bond between them. It forms when the carboxylic group of one amino acid molecule reacts and binds to the amino group of the other molecule.
Answer:
i gave u the link
Explanation:
https://docs.go ogle.com/document/d/16wFmesDrlt5C9kG3Zs mYXz8 cvEQiOYQvEZifbfgIUQM/edit#
