The answer is c steroids.
Answer:
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.
1. The C. elegans embryo as a system to study cell division
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.
Explanation:
There’s one hundred centimeters in one meter, and one thousand millimeters per meter.
that being said, 3000 mm are in 1 meter
Answer: B and D
Explanation: We can break down why the correct answers are choices B and D by understanding why A and C are incorrect.
Option A states that active transport utilizes channel proteins, and facilitated diffusion utilizes carrier proteins. This is incorrect. Active transport involves carrier proteins, and facilitated diffusion involves channel proteins. Carrier proteins are different from channel proteins in that, while channel proteins can only facilitate the passive diffusion of ions into or out of the cell along their concentration gradient, carrier proteins can also use ATP to move ions in or out of the cell against their concentration gradient.
This brings us to why option C is also incorrect. Option C states that both processes require the input of energy in the form of ATP. While active transport requires the use of ATP to transport ions with or against their concentration gradient, facilitated diffusion does not. This is easily remembered when we consider that active transport is called *active* transport because the cell is *actively* using energy to transport ions.
Hope this helped.
Answer:
The answer is c because A and B are not really giving off an imporant feeling to why carbon is important and D if you read the question carefully it says abundant which means to be a lot of, so C would be your answer
and plus i did the test
Explanation:
