The relationship is, the owl is the predator, and the mouse is prey.
Vomiting is a common symptom of the stomach flu - it starts a few hours after you're exposed to the virus so there isn't a certain amount of times you will vomit but drinking plenty of fresh, clean water will help you keep hydrated! :)
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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.
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The answer is 46 chromosomes.
Before mitosis, cell duplicates its DNA material so there are 46 chromosomes in duplicates and in total there are 46 x 2 = 92 sister chromatids. During mitosis, sister chromatids first join in the middle of the cell and then separate towards the opposite sides of the cell. After they separate, there are 46 sister chromatids on the one side and 46 sister chromatids on the other side. Each sister chromatid at the end of cytokinesis actually represents the chromosome of the newly formed daughter cell.
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