Answer:
in eukaryotic cells, the cytoplasm includes all of the material inside the cell and outside of the nucleus. All of the organelles in eukaryotic cells, such as the nucleus, endoplasmic reticulum, and mitochondria, are located in the cytoplasm.
Explanation:
"Waste" -- in the form of urine and feces -- how the body removes the parts of food we ingest that is not used for nutrition and also is a way to rid the body of toxins. The kidneys filter the blood, removing "waste" products such as excess vitamins or drugs (this is why your urine can have a bright color if you take high doses of vitamin c) and liquid waste is held in the bladder before being released. Food travels through the gut to be digested -- broken down into usable bits and waste. After breaking down in the stomach, the material travels through the small and large intestines. The small intestine is lined with villi -- tiny protrusions that add surface area so nutrients can be absorbed into the bloodstream. In the large intestine and colon, water is pulled from the mass so it becomes more solid. Eventually the solidified waste passed through the rectum and out the anus as feces. The build-up of waste in the body can itself be toxic -- if the kidneys do not function properly to clean the waste out, the buildup can be fatal. When the body goes into emergency mode to eliminate a toxic substance -- such as e. Coli in the case of food poisoning -- the intestines don't both absorbing water and the result is the liquid fecal matter being quickly passed through and ejected as diarrhea.
Answer:
Testcrosses clarify linkage because each phenotypic class of progeny corresponds to each gamete type produced by the dihybrid parent.
Explanation:
- A test cross involves the crossing of an individual with another phenotypically recessive individual so as to determine the zygosity of the former by analyses of the proportions of offspring phenotypes.
- In order to determine linkage, the test cross shows that if the parentals are more than the recombinants, we can say that the two genes such as b and c are genetically linked and therefore, they must be on the same chromosome.
- Also, the test-crosses help to find out which alleles came from which parent.
- By setting up testcrosses in which one parent is homozygous for the recessive alleles of both genes,we can analyze the gene combinations received in the gametes from the other, doubly heterozygous parent.
For most genes on the human X chromosome, 100% of XY males with mutant allele on the X chromosome will express the mutant phenotype.
50 % of human sperm cells that carry an X chromosome. There is 50 % chances that daughter of any male will not carry the gene and can't pass it on and 50 % chance that sons do not have the gene and it will be healthy. 50% chance that son have inherited the gene and express the trait or disorder.
If a Egg is fertilizes by sperm with X chromosome then zygote will be a female ' XX'. If the Egg is fertilizes by sperm with Y chromosome , then zygote will be male 'XY'.
To learn more about human sperm cells here
brainly.com/question/276208
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They both envole the earth
