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Damm [24]
1 year ago
10

The table below shows two conclusions about atoms based on experiments by Thompson and Bohr.

Biology
1 answer:
lilavasa [31]1 year ago
3 0

Researchers accept proposing speculations that negate current hypotheses. So, the proper alternative is D i.e., Scientists with varied experimental processes and interests perceive things differently.

As of late, the structure of molecules has been found. Sometime recently the perfect demonstration of a molecule was found, and a few others were proposed and abandoned.

In J.J. Thomson's theory, Thomson compared the definition of an iota to that of a Christmas pudding. He claimed that atoms are made up of an emphatically charged circle with inserted electrons.

Additionally, he claimed that since the sizes of positive and negative charges break even, an iota as an entirety is electrically impartial.

Rutherford tested with α-particle diffusing on a gold sheet. He took note that the lion's share of the negative particles did not divert when they voyage through the gold foil.

Learn more about atom theories at

brainly.com/question/13654549

#SPJ1

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Why does physarum polycephalum branch out like a plant or fungus?
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Answer:

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6 0
3 years ago
The CRISPR/Cas9 system can cleave genomic DNA at sequences other than the desired target, a phenomenon referred to as off target
Deffense [45]

Answer:

The minimum length of a sgRNA sequence to avoid off target cleavage by the CRISPR/Cas system in the fly fruit genome is 14 bases

Explanation:

We are trying to use the CRISPR/Cas system to cleavage the genome of the fruit fly (which is 1.4x10^8 bp long). Also we desire the cleavage to be unique. That means we need a target sequence long enough to be able to assume it will only appear once in the genome.

First, we should think that in every position, we can find one out of four different nucleotide (A, C, T, G). So, the probability of getting a sequence of a given length "n" will be (1/4)^n (We are assuming that the probability of finding a nucleotide in the position "i", it's independent of the nucleotide we find in any other position "j").

Also, to know how many times a sequence will appear in a genome (the expected value of occurrence), we must multiply the probability of that sequence to randomly occur by the length of the genome. For our specific example, the number of occurence of a sequence of length "n" is:

nºoccurence=[(1/4)^n]*1.4*10^8

But in this case, what we want is the expected number of times the sequence will appear to be 1, and we want to obtain the length of the target sequence (n).

Given the information above, we know that:

[(1/4)^n]*1.4*10^8 =1

[(1/4)^n]=(1/1.4*10^8)=1.4*10^-8

Then, if we want to calculate n, we can use logarithms and its properties to get:

log[(1/4)^n]=log[1.4*10^-8]

n*log[(1/4)]=log[1.4*10^-8]

n=log[1.4*10^-8]/log[(1/4)] => n=13.29 approximately.

As the sequence needs to have a natural number of elements, <u>we can conclude that using a target sequence of a minimum of 14 bases with the CRISPR/Cas system in the fly fruit genome should be enough to avoid off target cleavage.</u>

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4 years ago
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Explanation:

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