Answer:
It has oppistely charged ends
Answer:
The correct answer is - option C.
Explanation:
CFTR is a short form of cystic fibrosis transmembrane conductance regulator protein which is caused by a recessive mutation in this protein. This mutation results in the accumulation of mucus in secretory organs.
As the disease is a recessive disease, for the mutant phenotype to expressed both copies of the allele required to be recessive.
The mother is negative for the CFTR. Hence, she will not transfer the mutant allele to her child So, the child would have a wild-type phenotype even if the father having two copies of recessive allele.
Thus, the correct answer is - option C.
Humans get amino acids from protiens in the food we eat. As we digest the food, the enzymes in our stomach and small intestines break down proteins into small amino acids. So technically, we do not make amino acids, we get amino acids from eating food high in protiens.
Answer:Muscle cells are able to produce ATP with oxygen, which is called aerobic respiration, or without oxygen, an anaerobic process called anaerobic glycolysis or fermentation. The process in which ATP is made is dependent on the availability of oxygen (see the Cellular Respiration concepts).
Explanation:
