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levacccp [35]
3 years ago
11

Need help with these questions answer what you can

Biology
1 answer:
OlgaM077 [116]3 years ago
7 0

Answer 1:

The mutation shown is point mutation.

A point mutation can be described as a type of mutation in which only a single nucleotide of a sequence is either:

  • changed
  • added
  • deleted

The addition of the single nucleotide will cause the entire open reading frame to be changed. The amino acid sequence will change entirely from the position where the insertion mutation occurs. This is because the code for making amino acids works on a three base pattern. The reading of the three bases will be altered completely by the addition of just a single nucleotide.

Answer 2:

No, the resulting protein will not be altered.

The genetic code occurs in a linear sequence with triplet format. The change in a single base will cause the wrong amino acids to be formed. However, if the different code is common for the same amino acid then there will be no effect on the amino acid being formed.

<em>For example, the code GUA makes the amino acid Valine. If a mutation occurs and the code becomes GUU instead of GUA, then the resulting amino acid formed will also be Valine. Hence, there will be no alternation in the formation of the protein.</em>

Answer 3:

Melanoma cancer is the type of skin cancer which is associated with cancer from sun light. It is mainly caused due to the harmful ultraviolet rays which act as a mutagen.

<em>The mutations might keep coming back because although the growth have been removed, the other skin cells of the body might still have the mutation in them. As a result, growth will be seen again in the skin cells which might occur again and again. </em>

<em />

Explanation:

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A. True

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A colorimeter is an instrument used for chemical analysis by comparing a liquid’s color with standard colors. In an experiment,
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Answer:

The correct statements are that the first calorimeter is reliable but not valid, and the second calorimeter is valid and reliable.

Explanation:

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3 years ago
The human MN blood type is determined by two codominant alleles, L(M) and L(N). The frequency of L(M) in Eskimos on a small Arct
tatiyna

Answer:

(a) Frequency of M = 0.64

    Frequency of N = 0.04

    Frequency of MN= 0.32

(b)  Expected frequencies of M = 0.648

     Expected frequencies of MN = 0.304

     Expected frequencies of N =  0.048

Explanation:

(a) If random mating takes place in the population, then  the expected frequencies are

f(L(M)) = p = 0.8

F(L(N)) = q

q= 1 - p

= 1 - 0.8

= 0.2

Frequency of M = p^2 = ( 0.8)^2 = 0.64

Frequency of N = q^2 = (1-p)^2 = (1 - 0.8)^2 = (0.2)^2 = 0.04

Frequency of MN = 2pq = 2 * 0.8 * 0.2 = 0.32

(b)

F = inbreeding coefficient = 0.05

f(L(M)L(M)) = p^2 + Fpq = (0.8)^2 + 0.05 * 0.8 * 0.2 = 0.648

f(L(M)L(N)) = 2 pq - 2Fpq = 2 * 0.8 * 0.2 - ( 2 * 0.05 * 0.8 * 0.2) = 0.304

f(L(N)L(N)) = q^2 + Fpq = (0.2)^2 + ( 0.05 * 0.8 * 0.2) = 0.048

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Why human cell is consider as eukaryotic cell where as bacteria cell as prokaryotic cell?​
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They do not have a nucleus or membrane organelles
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