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Because RNA is composed of four parts of nucleotides, there are 43 = 64 possible codons, which is 64 possible triplets of nucleotides with several sequences. Furthermore, only 20 amino acids are commonly found in proteins so which, in most cases, a one amino acid is coded for through various dissimilar codons described in the figure. The genetic code is thus said to be degenerate. In reality, only methionine and tryptophan are shown by a single codon. As a conclusion of the genetic code's degeneracy, a mutation which changes only a single nucleotide in
Figure: The genetic code.
DNA point mutation, and thus changes only a single nucleotide in the corresponding mRNA, frequently has no effect on the amino acid sequence of the encoded polypeptide.
Define Technique of Paper chromatography? Paper chromatography is used as 1. Ascending, 2. Descending or 3. Horizontal technique (circular paper chromatography) It is De
Reducing Cost of Accident One clear way to control the cost of accident would be to follow all the rules of book for safety. All the methods of safety which were described ear
brief account on classification and general characters of protozoa
What is the mechanism of lipolysis?
Distribution of Stomata There are two parameters normally used for expressing the distribution of stomata. Stomatal frequency: The number of stomata per unit area
Q. Show the parameters which are of interest in CHD? Total Cholesterol: Serum totnl cholesterol equals the sum of HDL-cholesterol (HDL-c), VLDL-cholesterol (VLDL-c) and LDL-cho
What is a biosphere? A biosphere is a set of all of the ecosystems of the planet.
Q. Describe the effects of insulin on carbohydrate metabolism? Insulin promotes muscle glucose uptake and metabolism. In presence of insulin muscle cells take up glucose and us
Give three ways in which a polar bear is adapted to its environment. A polar bear is adapted to its environment by its high ratio of bulk to surface area, a thick water-repelle
How is the early diagnosis of genetic diseases usually done? Genetic disease might be diagnosed in the prenatal period by karyotype analysis, in case of aneuploidies, or by DNA
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