<h2>Answer is option "C"</h2>
Explanation:
- To clone a plant means to create an identical copy of an adult plant. These identical copies become young plants that in turn become adult plants that can be cloned again. This process can go on indefinitely
- The most common method of cloning plants and the one that has been used for a very long time is that of taking cuttings from an adult plant. A cutting is a stem or leaf that is cut from an adult plant. The cutting is then planted into moist soil or other moist growing media. The cutting will produce roots of its own and then become a whole new plant identical to the original adult plant. Not all plants can be cloned via cuttings, though
- Vegetative proliferation works in light of the fact that the finish of the cutting structures a mass of non-particular cells called a callus. With karma, the callus will develop, gap and structure different specific cells (roots, and so on.), in the end framing another plant
- Hence, the right answer is option C "Clone the plant"
The best answer is C
One of the jobs or functions of the Golgi apparatus is to process and bundle macromolecules like proteins as they are synthesized within the cell. The Golgi apparatus is sometimes compared to a post office inside the cell since one major function is to modify, sort, and package proteins to be secreted.
Golgi apparatus is an organelle present in most eukaryotic cells and is made up of membrane bound sacs . It is also referred to a Golgi body, Golgi complex or dictyosome.
I don’t understand your question.
It stabilizes ocean temperatures, creating a favorable environment for marine life
Answer:
The correct answer is A. autosomal recessive
Explanation:
In an autosomal disease, the mutation occurs in the autosomal chromosome, not in the sex chromosome. In autosomal recessive disease if both the defected allele from parent comes in the child then only the child would be affected by the disease. If the offspring have single defected allele than he is said to be a carrier.
So as the defect is not in sex chromosome the disease will occur in the same frequency in both the sexes and if parents are carriers which means they are not affected by disease than 25% offspring can have the disease because out of four offspring one can get both the defected allele, one from each parent. So the correct answer is A.
