Answer:
1. 80 chromosomes are found in each of the daughter cells. 2. Two daughter cells are produced. 3. The daughter cells are identical to each other.
Explanation:
Mitosis is simply a process of cell division whereby two daughter cells that are genetically identical are produced from a single parent cell. A cell having 80 chromosomes would undergo Mitosis through these various stages:
Interphase: This can be referred to as the rest phase between cell division when mature enough for reproduction. This is a preparatory stage where DNA is duplicated and ready for the division of chromosomes
Prophase: This stage marks the beginning mitosis of the cell with 80 chromosomes. The chromatin threads start a coiling process in which the chromosomes become condensed to enable easy distribution to daughter cells without tangling.
Prometaphase: This phase commences toward the end of the prophase, where the nuclear envelop breaks down. The chromosomes move toward to the center of the cell.
Metaphase: At this stage, the duplicated chromosomes line up on the mid plane or equator of the cell. During this stage, each chromatid is condensed completely and appears thick and distinct.
Anaphase: At this stage, the chromosomes move toward the poles as each replicated copies of the DNA of the cell ends up on either side of the cell. What we would have here at this stage is an entirely two new sister chromatid having 80 chromosomes. Cytokinesis begins towards the end of this stage as the parent cell cytoplasm divides which also continues at telophase.
Telophase: This is the final phase of Mitosis where two separate nuclei are formed and Cytokinesis takes place to complete the division of the cell to form two daughter cells having the same number of chromosomes. These cells are genetically identical to the original parent cell.
Answer:
Cells are the basic unit of matter is the correct answer.
Explanation:
The other answers are all a part of the cell theory, but that one is NOT and since the question is asking for the incorrect one, that's the answer. :)
Answer:
In strict mode, the narrow-sense heritability is the proportion of the additive genetic variance that contributes to the total of the phenotypic variance. This value can be associated with the inheritance of the a-thalassemia
.
Explanation:
A-thalassemia is a genetic disorder caused by mutations affecting four different genes that encode alpha-globin, thus affecting the hemoglobin production process and, consequently, oxygen transport. The mode of inheritance of the a-thalassemia may be associated with narrow sense heritability since the phenotype is manifested by gradation, i.e., each allele might contribute in similar mode to this genetic condition.
True is the correct answer
Answer:Cells are the basic building blocks of all living things. ... Cells also contain the body's hereditary material and can make copies of themselves. Cells have many parts, each with a different function. Some of these parts, called organelles, are specialized structures that perform certain tasks within the cell.
Explanation:look it up
