Answer:
The one with A is 35%
Explanation:
there is usually a 50 50 of cg and at so a would add with 15% to make 50%
Answer:
A gene mutation can be described as errors in the nucleotide sequence of a gene due to errors in the DNA replication process or due to any mutagen. On the other hand, a chromosomal mutation can be described as a change in the structure of a DNA or changes in the number of chromosomes.
A gene mutation occurs in a single gene whereas a chromosomal mutation will affect many genes. Hence, gene mutations will be comparatively less lethal than chromosomal mutations.
Example of gene mutation: Sickle cell anemia
Example of chromosomal mutation: Down's Syndrome
Answer:
what is black death clear it first
C. <span>The more greenhouse gases that are in the atmosphere, the more heat will be trapped. That means earth’s energy budget could be disturbed because the amount of heat radiating toward the surface is greater than the amount of heat escaping from the earth</span>
Answer:
- Calcium binds to troponin C
- Troponin T moves tropomyosin and unblocks the binding sites
- Myosin heads join to the actin forming cross-bridges
- ATP turns into ADP and inorganic phosphate and releases energy
- The energy is used to impulse myofilaments slide producing a power stroke
- ADP is released and a new ATP joins the myosin heads and breaks the bindings to the actin filament
- ATP splits into ADP and phosphate, and the energy produced is accumulated in the myosin heads, starting a new cycle
- Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.
Explanation:
In rest, the tropomyosin inhibits the attraction strengths between myosin and actin filaments. Contraction initiates when an action potential depolarizes the inner portion of the muscle fiber. Calcium channels activate in the T tubules membrane, releasing <u>calcium into the sarcolemma.</u> At this point, tropomyosin is obstructing binding sites for myosin on the thin filament. When calcium binds to troponin C, troponin T alters the tropomyosin position by moving it and unblocking the binding sites. Myosin heads join to the uncovered actin-binding points forming cross-bridges, and while doing so, ATP turns into ADP and inorganic phosphate, which is released. Myofilaments slide impulsed by chemical energy collected in myosin heads, producing a power stroke. 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. Finally, Z-bands are pulled toward each other, shortening the sarcomere and the I-band, producing muscle fiber contraction.
