Answer: I believe you need to examine the layers, the color, texture.
<span>DNA contains the code for all an organism's protein. Since many of the organism's structures, processes, and growth depend on protein the DNA is central to the well being of all organisms. In eukaryotes, the DNA is locked up in the nucleus. The area of the cell where proteins are made is in the cytosol (ribosomes). In order for the protein to be made the DNA has to produce a copy of the blueprint m-RNA. This messenger RNA will take the code to the ribosome. The process by which m-RNA is made is called transcription. A-U, C-G base pairing rules. Once on the ribosome another RNA comes into play t-RNA. This is called transfer RNA. Here it will take an amino acid and place it in the correct order to produce the desired protein. This is called translation. It begins with a start co don AUG. and ends with a stop codon. The protein will then go to the Golgi apparatus and be formed into its final shape.
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The probability that they both were planted alone is 0.3325.
<h3>What is genetic probability?</h3>
Probability serves to mathematically estimate the possibility of events that happen by chance, that is, as a matter of luck.
In this case:
- Number of plants planted alone = 134
- P(both plants were planted alone) = 134/232 x 133/231 = 0.3325
So the probability that both were planted alone is 0.3325.
See more about genetic probability at brainly.com/question/851793
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Answer:
In strict mode, the narrow-sense heritability is the proportion of the additive genetic variance that contributes to the total of the phenotypic variance. This value can be associated with the inheritance of the a-thalassemia
.
Explanation:
A-thalassemia is a genetic disorder caused by mutations affecting four different genes that encode alpha-globin, thus affecting the hemoglobin production process and, consequently, oxygen transport. The mode of inheritance of the a-thalassemia may be associated with narrow sense heritability since the phenotype is manifested by gradation, i.e., each allele might contribute in similar mode to this genetic condition.
