Answer:
Explanation:
DNA is deoxyribose nucleic acid. It is a double helical structure. It remains in the coiled form so as to make the information stored in the small region within the cell. The sequence of bases allows the information to be stored in the coded form so as to promote the synthesis of proteins. Complementary base pairing allows the DNA molecule to replicate itself.
<h2>Down Syndrome</h2>
Explanation:
Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
- Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
- Down syndrome is usually caused by an error in cell division called nondisjunction which results in an embryo with three copies of chromosome 21 instead of the usual two
- Prior to or at conception, a pair of 21st chromosomes in either the sperm or the egg fails to separates
- With development in embryo the extra chromosome is replicated in every cell of the body;this type of Down syndrome which accounts for 95% of cases is called trisomy 21
- Maternal age is the only factor that has been linked to an increased chance of having a baby with Down syndrome resulting from nondisjunction;here environmental agents such as drugs, chemicals, and radiation act as mutagens which induce mutation in the fetus
I believe the answer you're looking for is cellular respiration.
Answer:
Explanation:
Mendel's law of independent assortment state that two different genes assort independently in gamete formation.
To reach this conclusion, one has to do a dihybrid cross. This means that two genes responsible for different traits need to be analyzed at the same time.
1) Starting with a <u>parental generation of a cross between two pure lines</u> (homozygous for both genes) <u>with different traits</u>, a plant with yellow and round seeds (YYRR) and another with green and wrinkled seeds (yyrr). <u>The F1 will be phenotypically homogeneous (</u>yellow and round)<u>, and genotypically heterozygous (</u><u>YyRr</u><u>)</u>.
2) If the individuals from the F1 are crossed with one another, we have to do a Punnett Square to determine the phenotypic ratio of the F2.
- If the genes assort independently, the F1 individuals will produce their different gametes with the same probability. Each possible gamete will appear in a 1/4 proportion: YR, Yr, yR, yr.
- The 9:3:3:1 ratio is a result of analyzing the possible phenotypes that result from the dihybrid cross.
See the attached image for an illustration of the crosses in each generation and the Punnett Square.
There are several specific characteristics for procaryote and eucaryote:
- Procaryotes has a cell wall, in addition to the cell membrane.
- procaryotes has chromatin in the cytoplasm, they do not have a nucleus.
- Procaryotes are small cells visible only at the microscope with x100 objective.
About the eucaryotic cells:
- Eucaryotes have mitochondria,
- Eucaryotes have endoplasmic reticulum
- Eucaryotes have a nucleus with DNA chromatin and nucleoli inside it.
- Eucaryotes are visible in the microscope x40