Answer:
The physical stimulus is the only part of the test that is measureable, and therefore, knowable. The stimulus is our anchor for our estimate of the listener's perception.
D. the floodplain shrinks
Answer:
<u>Structure G</u> is Option (c) : Vacuole
<h3><u>Connective tissue:</u></h3>
It is the layer under the epithelial tissue in the body. It is stronger than epithelial tissue and is found in many organs. It provides protection.
<h3><u>Epithelial tissue:</u></h3>
It covers the outside of the body like a veil. located in the outermost part of the body. Protects the body against microbes and infections.
<h3><u>Muscle tissue:</u></h3>
It is located in the joint areas and forms the support and movement system. It allows us to make bodily movements.
<h3><u>Nervous tissue:</u></h3>
It is the fastest communication tissue. It allows us to feel pain and the sense of touch. It is impossible to repair this tissue after it is damaged. It causes paralysis. It is very important as it plays a role in the activity of neural transmission.
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: