the answer would be B because that were percipitation starts at
The advantage gained by staining cells are the following:
- provides a better and clear image of the cell's structure
- staining will help in differentiating the different parts of the cell
- this will enhance its view under the microscope.
A substitution is a mutation that exchanges one base for another (i.e., a change in a single "chemical letter" such as switching an A to a G). Such a substitution could: change a codon to one that encodes a different amino acid and cause a small change in the protein produced. ... These are called silent mutations.
784109 People per sq. mi land would its people need if the population density is 3,826 people/km2.
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What is population density?</h3>
The density of individuals within a species in a given geographic location is referred to as population density. Data on population density can be used to calculate demographics and examine interactions with ecosystems, human health, and infrastructure.
The population density equation below can be used to calculate the population density of a piece of land:
Population Density = Population/ Area
The residential density is important in determining the people's thinking and culture. Engineers find it vital to forecast population growth in order to develop infrastructure that can support a large population. It is practically impossible to develop a perfect 3D model of any structure that allows the largest number of people to live without this understanding.
For more information regarding population density, visit:
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Answer:
Alfred Hershey and Martha Chase
Explanation:
In 1952 Alfred Hershey and Martha Chase were working with bacteriophages or phages, which are viruses that infect bacteria. They knew that a phage had an outer shell of protein and an inner core of DNA. In addition, from the electron microscope observations, they also knew that during infection the virus attacks the bacterium by its tails and introduces its genetic material into the bacterium to multiply using its metabolic machinery. They radioactively labeled two sets of phages: one with 32P (which marks only DNA) and another with 35S (which marks only proteins). In two parallel experiments, they infected bacteria with viruses marked on their DNA and with viruses marked on their proteins. The cultures were shaken with a mixer to separate the virus particles from the bacterial coatings. They then performed a centrifugation to separate the phages from the bacteria, so that the larger and heavier bacteria remain in the pellet, while the phages remain in the supernatant. They found that the radioactivity of 35S appeared in the supernatant while that of 32P appeared in the sediment, from which new radioactively labeled virus particles appeared, demonstrating that DNA was the genetic material.
