Answer:
Tropomyosin
Explanation:
The calcium binding to troponin and induces the muscle contraction. The active binding site gets exposed due to the calcium binding.
The calcium ions then attaches with troponin molecule. This changes the shape of troponin and removes the tropomyosin protein from the binding site. No ATP is available during this process.
Thus, the correct answer is option (d).
The correct answer is: daughter cells will have abnormal chromosome numbers and this condition is called aneuploidy.
Nondisjunction is the failure of homologous chromosomes (or sister chromatids) to separate during the process of cell division and consequently lead to aneuploidy. There are three forms of nondisjunction:
• Nondisjunction in meiosis I (pair of homologous chromosomes unable to separate in meiosis I),
• Nondisjunction in meiosis I (sister chromatids unable to separate during meiosis II), and
• Nondisjunction in mitosis (failure of sister chromatids to separate during mitosis)
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This would depend on if the other parents has it or not. If they do not, they have a 50/50 chance that the trait will become recessive. That said, it could still be passed on to the child's kids in later generations.
Yes, when the egg and a sperm cell meet fertilization has taken place
