The right answer is B.
Starch is, along with cellulose, the most common polysaccharide in the plant world. It constitutes the essential energy reserves of plants and is a component of the diet of humans. It is part of the group of slow sugars. Its consumption is particularly recommended to those who practice a sport.
Glycogen, which is a polysaccharide, is the form in which carbohydrates are stored in the body (animals and fungi). Glycogen is broken down into glucose molecules when the body needs energy.
Answer:
The answer is: Receptor A because the ligand concentration is greater than the Kd.
Explanation:
Receptor A because the ligand concentration is greater than the Kd., because the conformation of a receptor protein composes the functional state. Ligands include substrates, inhibitors, activators, and neurotransmitters. So, Affinity is a measure of the strength of attraction between a receptor and its ligand.
Answer:
the answer is b.The model should show the original stem cell dividing to become a differentiated cell and another stem cell.
Explanation:
Answer:
If the shape of an enzyme changes then the enzyme will no longer be able to perform its function.
Enzymes can be described as bio-catalysts which usually speed up a chemical reaction. Each enzyme has a particular substrate which fits into the active site of the enzyme. Every enzyme needs a particular temperature and pH for its functioning. If the shape of an enzyme changes, then it will no longer be able to perform its function and will become denatured.
Mitosis is used for almost all of your body’s cell division needs. It adds new cells during development and replaces old and worn-out cells throughout your life. The goal of mitosis is to produce daughter cells that are genetically identical to their mothers, with not a single chromosome more or less. Meiosis, on the other hand, is used for just one purpose in the human body: the production of gametes—sex cells, or sperm and eggs. Its goal is to make daughter cells with exactly half as many chromosomes as the starting cell. To put that another way, meiosis in humans is a division process that takes us from a diploid cell—one with two sets of chromosomes—to haploid cells—ones with a single set of chromosomes. In humans, the haploid cells made in meiosis are sperm and eggs. When a sperm and an egg join in fertilization, the two haploid sets of chromosomes from a complete diploid set: a new genome.In many ways, meiosis is a lot like mitosis. The cell goes through similar stages and uses similar strategies to organize and separate chromosomes. In meiosis, however, the cell has a more complex task. It still needs to separate sister chromatids (the two halves of a duplicated chromosome), as in mitosis. But it must also separate homologous chromosomes, the similar but nonidentical chromosome pairs an organism receives from its two parents. These goals are accomplished in meiosis using a two-step division process. Homolog pairs separate during the first round of cell division, called meiosis I. Sister chromatids separate during a second round, called meiosis II. Since cell division occurs twice during meiosis, one starting cell can produce four gametes (eggs or sperm). In each round of division, cells go through four stages: prophase, metaphase, anaphase, and telophase.Before entering meiosis I, a cell must first go through interphase. As in mitosis, the cell grows during G_1 1 start subscript, 1, end subscript phase, copies all of its chromosomes during S phase and prepares for the division during G_2 2 start subscript, 2, end subscript phase. During prophase, I, differences from mitosis begin to appear. As in mitosis, the chromosomes begin to condense, but in meiosis I, they also pair up. Each chromosome carefully aligns with its homolog partner so that the two match up at corresponding positions along their full length. For instance, in the image below, the letters A, B, and C represent genes found at particular spots on the chromosome, with capital and lowercase letters for different forms, or alleles, of each gene. The DNA is broken at the same spot on each homologue—here, between genes B and C—and reconnected in a criss-cross pattern so that the homologs exchange part of their DNA.This process, in which homologous chromosomes trade parts, is called crossing over. It's helped along by a protein structure called the synaptonemal complex that holds the homologues together. The chromosomes would actually be positioned one on top of the other—as in the image below—throughout crossing over; they're only shown side-by-side in the image above so that it's easier to see the exchange of genetic material.
