Answer:
because if they dident stop it would malfunction
Explanation:
An individual having two different alleles of a specific gene is described as being Heterozygous for that specific trait.
You have a heterozygous genotype for that gene if the two versions differ. Being heterozygous for hair color, for example, means you have one allele for red hair and one allele for brown hair. The interaction of the two alleles influences which traits are expressed.
Being homozygous for a gene means you inherited two identical copies. It is the inverse of a heterozygous genotype, in which the alleles differ. People with recessive characteristics, such as blue eyes or red hair, are always homozygous for that gene. In genetics, heterozygous means having inherited different versions (alleles) of a genomic marker from each biological parent. As a result, a person who is heterozygous for a genomic marker has two distinct versions of that marker.
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Answer:
A
Explanation:
i guessed ona quiz and got it right.
The correct sequence of these events (origin of mitochondria, origin of multicellular eukaryotes, origin of chloroplasts, origin of cyanobacteria, origin of fungal-plant symbioses), from earliest to most recent, in the evolution of life on earth is 4, 3, 1, 2, 5.
The transition to eukaryotic cells seems to have taken place in the Proterozoic Era, around 1.2 to 1.5 billion years ago. Nevertheless, the latest genetic studies propose the divergence of eukaryotes from prokaryotes nearer to 2 billion years ago.
Margulis suggested the mechanism of endosymbiosis, to describe the origin of mitochondria as well as chloroplasts from persistent living prokaryotes. In accordance with this idea, a bigger prokaryote engulfed or enveloped a smaller prokaryote around 1.5 billion to 700 million years ago.
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Answer:
Sample A: 21.3%A, 28.7% G and 28.7% C
Sample B: 27.7% A, 22.3% G and 22.3% C
Explanation:
According to Chargaff's rules of base pairing, the amount of adenine in a DNA molecule equals the amount of thymine, and the amount of G=C.
<u>Sample A</u>
Contains 21.3% T, so it also contains 21.3% A. Therefore A+T= 42.6%
100% - (A+T) = (G+C)
100% - 42.6% = 57.4%
G+C add up to 57.4% of the DNA in sample A. And because G=C, there's 28.7% G and 28.7% C.
<u>Sample B</u>
Contains 27.7% T, so it also contains 27.7% A. Therefore A+T= 55.4%
100% - 55.4% = 44.6%
G+C add up to 44.6% of the DNA in sample B.
And G=C, so there's 22.3% G and 22.3% C.
