TCATGAC that would be the other half of the dna strand
Answer:
they are not affected by earth atmosphere
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: A specific chemical binding to nociceptors
Explanation:
Answer:
One-half of the daughters of an affected man would have this condition.
Explanation:
Each daughter born to a woman that is positive for a dystrophin mutation on one of her two X chromosomes possess a 50 percent likelihood of possessing the mutation and also becoming a carrier. Carriers at times do not show the disease symptoms but may give birth to a child that has the mutation or the disease condition. DMD carriers do have a higher chance of cardiomyopathy.
A man with DMD cannot transfer the affected gene to his sons since he passes to his son a Y chromosome, not the X chromosome. But he will definately transfer it to his daughters, since each daughter possess her father’s only X chromosome resulting in the daughters being carriers.
Hence, One-half of the daughters of an affected father and a carrier mother could have this condition.
