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dmitriy555 [2]
3 years ago
15

The more particles that are hitting each other in a fluid, the less pressure is created.

Biology
2 answers:
Kazeer [188]3 years ago
7 0

Answer:

False

Hope this helps!

Kipish [7]3 years ago
6 0

Answer:

The person above is correct, this is false.

Explanation:

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In a sample population of people, 36% have the recessive trait of "free" earlobes (q2). What is the frequency of the dominant al
ICE Princess25 [194]

Answer:

Explanation

Given that 36% are recessive in traits

100-36 = 64% for dominant traits considering a whole population to be 100%

P=dominant allele

q= recessive allele

P2= dominant genotype

q2= recessive genotype

according to hardyweinberg principle, p+q=1

64/100= 0.64 frequency for dominant traits or genotype, therefore

p2=0.64

then

P=√0.64

p= 0.8

Therefore, dominant allele frequency (p) for the population is 0.8

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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:

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