Answer:
Animal Waste and Fertilizers
Explanation:
Animals, like humans, obtain nitrogen from consuming foods. The foods that the animals consume get digested and with time, the animals release the extra undigested foods and nutrients in forms of urine and feces. Like wise, fertilizers are typically made with animal waste.
The parent plant produced asexually because offspring from asexual reproduction are genetically identical to the parent.
Answer:
The inputs can be material, such as the silicon used in the computer chips in a phone, or energy, which is used, for example, to manufacture and operate a phone. Outputs can be usable products or wastes, which must be disposed or recycled. A life cycle analysis of a cell phone also includes an analysis of its individual parts.
Explanation:
Hope this helps!!!
-BB
Answer:Yes
Explanation:
Only if someone down their bloodline has had 3 eyes. It would be possible, but highly unlikely.
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>.
