The cellular respiration happens in the mitochondria. During the cellular respiration, glucose and oxygen are the reactants during this process and the main product of this process is ATP, with waste products carbon dioxide and water. Therefore, the correct answer would be option B. O2 (oxygen) and C6H1206 (glucose).
3 examples of proteins in living organisms:
1. Collagen - maintains firmness and structure to body cells and tissues, keeping them together.
2. Keratin - creates the protective barrier for living organisms like skin, nails, and hair.
3. Globular and trans-membrane - supports the regulation of the flow of small ions and molecules such as sodium and glucose.
Answer:
The zebra mussels also outcompete the natives for food and space, and because of their fast reproduction can quickly overwhelm a water system.
Explanation:
The feeding habits of zebra mussels can also have a drastic impact on an infested lake. Zebra mussels are filter feeders that siphon particles of plankton from the water.
To first dive into your question, here are some vocabulary terms that I will be using and will be helpful to you as well.
- Homozygous dominant (BB): <em>Is not affected by cystic fibrosis</em>.
- Homozygous recessive (bb):<em> Is affected by cystic fibrosis</em>.
- Heterozygous (Bb):<em> A carrier for cystic fibrosis</em>.
- Phenotype (Ex: Having cystic fibrosis): <em>The appearance of an allele pair</em>.
- Genotype (Ex: bb): <em>The genetic makeup of an allele pair</em>.
We know that if both of the parents are phenotypically normal, there is no way that they can be homozygous recessive (bb), or have cystic fibrosis. We also know that since they have a child with this disease, they can't be homozygous dominant (BB) either. This means that <u>both parents have to be carriers (Bb)</u> in order for them to have a child with cystic fibrosis.
Below I have attached a Punnett square with both of the heterozygous parents.
<em>Each child they have will have a </em><u><em>1/4</em></u><em> or </em><u><em>25%</em></u><em> chance of having cystic fibrosis.</em>
Answer:
food and physical activity choices, some medications, and skipping or not taking enough glucose-lowering medication