She will need A. Bean seed that gets no fertilizer.
I hope this helps! :D
Answer:
Sickle cell anemia is an inherited condition in which there aren't enough healthy red blood cells to carry oxygen through an individual's body. The red blood cells of a healthy individual are flexible and round, and they move through blood vessels with no problem, transporting oxygen successfully. However, a person with sickle cell anemia has rigid, sticky red blood shaped like sickles or crescent moons. These cells often get stuck in small blood vessels, which can slow or block blood flow and oxygen delivery to different parts of the body.
The sickle cell anemia trait is found on a recessive allele of the hemoglobin gene, while the regular red blood cell trait is found on the dominant allele. This means that a person must have two copies of the recessive allele (one from their mother and the other from their father) to be born with this condition. People who have one dominant and one recessive allele or both dominant alleles will have healthy red blood cells.
Answer:
The change in time for the first quarter is 2.07 seconds.
The change in time for the second quarter is 1.09 seconds.
The change in time for the third quarter is 0.95 seconds.
The change in time for the fourth quarter is 0.81 seconds.
Explanation:
This is for table C
Answer:
With respect to the differences in the DNA sequence of six species, including the human one, it is true that the DNA sequences may vary but the aminoacid sequences are identical.
Explanation:
Options for this question:
- <em>The DNA sequences may vary but the amino acid sequences are identical.
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The nitrogen bases in the nucleotides must also be different in each.
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The process in producing additional DNA, replication, is identical in all six.
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The process of producing DNA, or replication, varies due to the differences in the DNA codes.
The different species that exist have specific genomes for each of them, this is the <u>genetic information contained in the DNA varies from one species to another</u>, as can be seen in the scheme (see image). However, the genetic code is universal, and does not vary from one species to another.
The genetic code is found in the RNA molecule and is a sequence of nucleotides that, organized in triplets (codons), are responsible for the synthesis of specific amino acids. An RNA molecule contains the information necessary for protein synthesis.
The scheme shows the differences of five species with respect to the human, based on the respective DNA sequences. But what it does not show is a universally accepted truth, that the nucleotide sequence encoding an amino acid is the same for each of these species.
Learn more:
Genetic code brainly.com/question/15338
<span>Disaccharides need to be broken down into their component subunits (monosaccharides) before their absorption. The reaction that breaks them up is hydrolysis and it is done by enzymes- <span>glucosidases. Glucosidases are located on the brush border of the small intestine, attached to the surface of the epithelial cells. After the catalyzation of these disaccharides, the epithelial cells take up the monosaccharides and transport them inside using ATP energy. From there they are transported into the bloodstream.</span></span>
