Answer:
Alloy is a mixture made up of iron &nickel.
Answer:
Part A....B
Part B....C
Explanation:
It should be understood that Mice are always first used to clinical test especially for drugs or other things that are supposed to be for human use, this is because Mice and human genetic disorders have arisen from conserved and related evolutionary processes. Therefore, when the clinical trial or test produces a positive result in the Mice, it is almost certain that the result will be the same in human.
Now in part B. When the result result is different, it might be because of the differences in anatomy and physiology might hide or change development and symptoms of disease. And that is the reason why, the result of a particular drug differs from person to person.
Answer:
When a muscle cell contracts, the myosin heads each produce a single power stroke.
Explanation:
In rest, attraction strengths between myosin and actin filaments are inhibited by the tropomyosin. When the muscle fiber membrane depolarizes, the action potential caused by this depolarization enters the t-tubules depolarizing the inner portion of the muscle fiber. This activates calcium channels in the T tubules membrane and releases calcium into the sarcolemma. At this point, <em>tropomyosin is obstructing binding sites for myosin on the thin filament</em>. When calcium binds to the troponin C, the troponin T alters the tropomyosin by moving it and then unblocks the binding sites. Myosin heads bind to the uncovered actin-binding sites forming cross-bridges, and while doing it ATP is transformed into ADP and inorganic phosphate which is liberated. Myofilaments slide impulsed by chemical energy collected in myosin heads, <u>producing a power stroke</u>. The power stroke initiates when the myosin cross-bridge binds to actin. As they slide, ADP molecules are released. A new ATP links to myosin heads and breaks the bindings to the actin filament. Then ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, which starts a new binding cycle to actin. Z-bands are then pulled toward each other, thus shortening the sarcomere and the I-band, and producing muscle fiber contraction.
