The answer is 46 chromosomes.
Before mitosis, cell duplicates its DNA material so there are 46 chromosomes in duplicates and in total there are 46 x 2 = 92 sister chromatids. During mitosis, sister chromatids first join in the middle of the cell and then separate towards the opposite sides of the cell. After they separate, there are 46 sister chromatids on the one side and 46 sister chromatids on the other side. Each sister chromatid at the end of cytokinesis actually represents the chromosome of the newly formed daughter cell.
The fetus can be screened for abnormalities using karyotyping and biochemical analysis using amniocentesis and chorionic villus sample.
<h3>What data can we glean from CVS and amniocentesis?</h3>
In at-risk fetuses, these tests can detect genetic illnesses such cystic fibrosis, Tay-Sachs disease, and sickle cell disease. The main benefit of CVS over amniocentesis is that it is done considerably earlier in pregnancy—at 10 to 13 weeks as opposed to 15 to 20 weeks—thus saving more time for the mother.
<h3>What can a couple learn about their growing fetus from amniocentesis and chorionic villus sampling?</h3>
Amniocentesis and chorionic villus sampling (CVS) are prenatal diagnostic techniques used to identify certain fetal genetic disorders. The likelihood of miscarriage rises with both procedures.
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The cleanliness of a ecosystem or how healthy it is. It determines how clean an environment/ecosystem is. You need all types of animals living there, therefore making it more healthy. The more healthy, the more we can say that it is biodiverse.
Answer:
Ribosomes are found 'free' in the cytoplasm or bound to the endoplasmic reticulum (ER) to form rough ER. In a mammalian cell there can be as many as 10 million ribosomes. Several ribosomes can be attached to the same mRNA strand, this structure is called a polysome.
Explanation:
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