Answer:
digestion
Explanation:
breaking down of food particles into smaller substance is known as digestion.
The molecules doesn't need energy to cross through.
The diffusion doesn't need protien, the molecules pass between phospholipids by passes protien. It moves smaller molecules. Facilitated need protien also hormone, and larger molecules.
I wish it makes sense.
Answer:
yes
Explanation:
It depends upon the fertility of the bird.When a poultry bird is raised the farmer provides the bird with food supplement with other vitamins and some leafy vegetables.This enables the good growth and fertility rate and capability is increased through it.Hence,A poultry bird can lay more eggs in a day.
<em>Keep</em><em> </em><em>smiling </em><em>and</em><em> </em><em>hope</em><em> </em><em>u</em><em> </em><em>r</em><em> </em><em>satisfied </em><em>with</em><em> </em><em>my</em><em> </em><em>answer</em><em>.</em><em>Have</em><em> </em><em>a</em><em> </em><em>nice</em><em> </em><em>day</em><em> </em><em>:</em><em>)</em>
Answer:
1. At the end of S phase- 20 pg DNA
2. At the end of G2 phase- 20 Pg DNA
Explanation:
The cell before undergoing M phase undergoes the steps of interphase that is G₁, S and G₂ phase.
During S phase, the process of cell replication takes place which replicates the DNA as a result of which the amount of DNA doubles. This DNA amount is reduced to half during the anaphase stage of M phase.
In the question since the amount of DNA is 10pg therefore the amount will be double during S phase and becomes 20 pg and will remain 20 pg until the DNA is distributed therefore at the end of G₂ phase Will remain the 20 pg.
Answer: The receptor site is the location that a drug binds to, altering the function of a biomolecule.
Explanation:
The drug receptors site, are the sites where the sites where the drug molecules bind. Basically, a low number of receptors exists and the extent to which the molecules occupy their sites differ with the concentration of drug. The receptor site changes the conformation and function of the binding molecule of the drug.
