Because bacterial life cycle is very short it complete in 20 minutes to produce copies. secomdly bacterial genome is simple to be handle.
<span>The energy which we are using in today's world for our needs is fossil fuel, we used to power our home by burning coal and run our vehicle through the oil or fossil fuel, but we should know that it is limited in quantity and cannot use it once it releases energy or burned, it is created by the dead organic materials like trees and animals etc. which slowly buried in the ground as the time goes and after 1000's of years it get pressurised and rise in temperature make that organic material into fossil fuel, so that's how the fossil fuel comes in existence, which we extract from the ground by drilling deep into the ground.</span>
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Yes
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Because they are being helpful so that te other wolfs don't get attacked over the food.
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If it is tested in a controlled setting with repeated results
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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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