Answer:
48 amino acids
Explanation:
The wild type gene codes for a protein with 100 amino acids. One amino acid is encoded by one triplet code of the gene. This means that the wild type gene has a total 100 triplets or 300 nucleotides to code for a protein of 100 amino acid. Mutation in this protein has introduced the code "UAA" at the 49th codon. The code "UAA" is a stop codon. Therefore, the mRNA transcribed from the mutant allele would code for a protein having 48 amino acids as the protein synthesis will be stopped once the stop codon at the 49th position is read.
"Prophase I" is the stage of meiosis that synapsis and the formation of tetrads occur.
Answer:
The nucleus
Explanation:
Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA). Mitochondria are structures within cells that convert the energy from food into a form that cells can use.
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Answer:
Lysosomes.
Explanation:
HEXA (Hexosaminidase A) is the functional enzyme and encoded by the HEXA gene. The main function of this enzyme is the hydroxylation of the gangliosides.
The mutation in this gene leads to the lysosomal storage disease. The GM2 starts accumulating in the lysosomes and causes Tay Sach's disease. This is a genetic disorder that leads to the breakdown of the cells of the spinal cord and the brain.
Thus, the answer is lysosomes.
Cycloalkanes
are saturated hydrocarbons with monocyclic structure.
<span>This
means that cycloalkanes contain hydrogen and carbon atoms arranged in a
structure containing a single ring (sometimes with side chains), with all of
the carbon-carbon bonds single. The examples of cycloalkanes are cyclopropane,
cyclobutane, cyclopentane, cyclohexane…</span>
