The average height of the oceans surface between high and low tides is called the sea level. It is important to know this measurement because with this it is possible that we can calculate the height of anything on the land. Also, we can <span> calculate the height of anything on the land. Also, we can be able to determine whether the oceans are falling or rising through time.
So the answer is </span><span>Sea level </span>
People who advertises items or things to put there ideas out there.
The answer is "<span> It has all cell types found in other forms of connective tissue."
The areolar tissue situated in the skin ties the external layers of the skin to the muscles underneath. Areolar tissue is additionally found in or on mucous layers, and around veins, nerves, and the organs of the body.
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I’m pretty sure males are ZZ. Let me know if I’m right and have a good rest of your day!
Answer:
1. The difference between the normal hemoglobin protein DNA sequence and the sickle cell hemoglobin DNA sequence is a base to base shift, in this case adenine (GAG) to thymine (GTG).
2. The difference affects the amino acid sequence of the protein by replacing glutamic acid (Glu) with valine (Val).
Explanation:
In sickle cell anemia, a change in the DNA nucleotide sequence is observed, where adenine is substituted by thymine, whose expression is the change in the amino acid sequence of globine β, incorporating valine instead of glutamic acid. This represents a molecular mutation - point mutation - by subtitution, which corresponds to missense mutation.
<u>Normal hemoglobin protein in a RBC</u>
DNA CTG ACT CCT GAG GAG AAG TCT
Amino acids Leu Thr Pro Glu Glu Lys Ser
<u>Sickle cell hemoglobin protein in a RBC</u>
DNA CTG ACT CCT <em>GTG</em> GAG AAG TCT
Amino acids Leu Thr Pro <em>Val</em> Glu Lys Ser
When GAG is transcribed to mRNA, the CUC codon is obtained, which codes for glutamic acid. Thymine substitution causes the DNA sequence to change to GTG, which is transcribed as CAC, the codon that encodes the amino acid valine. The <u>change from glutamic acid to valine in β-globin causes an altered hemoglobin, giving the abnormal erythrocytes observed in sickle cell disease</u>.
