Answer:
B
Explanation:
Wall cell has to be strong to bring protection to the cell. In general it is made of beta-glycosidic bonds.
Storage polysaccharides, are a source of available energy for the cell in any moment. Therefore, the bonds of storage polysaccharides need to be weak. In that way, when the cell needs energy from carbohydrates, it is not going to spend so much energy trying to break the bond.
Answer:
It has incomparable advantages over other gene editing tools.
Explanation:
For example, the CRISPR-Cas9 system has more target sites than ZFNs and TALENs, and Cas9 has many variants that can be used in a variety of studies. Moreover, the system is extremely easy to use and can be executed in almost any laboratory.
The most important advantages of CRISPR/Cas9 over other genome editing technologies is its simplicity and efficiency. Since it can be applied directly in embryo, CRISPR/Cas9 reduces the time required to modify target genes compared to gene targeting technologies based on the use of embryonic stem (ES) cells.
Disadvantages of CRISPR technology: CRISPR-Cas9 off-target; The effect of off-target can alter the function of a gene and may result in genomic instability, hindering it prospective and application in clinical procedure.
this the best i got, hope it helps :)
Okay so there are two types of ERs, smooth and rough.
Rough endoplasmic reticulum contain ribosomes on the outer surface. It provides large surface area for proteinsynthesis and the synthesis of glycoproteins and also provides a pathway for the transport of materials.
Smooth ER synthesises, stores and transports lipids and carbohydrates.
Hope this helps
The correct answer for the question that is being presented above is this one: "B. extra chromosome 21." Karyotypes can be studied to determine an organism’s chromosomal makeup and to detect genetic defects. Down syndrome is a genetic disorder that is also called trisomy 21. Trisomy 21 look like in a karyotype with <span>extra chromosome 21</span>
The answer is A "the first four steps of meiosis" because in mitosis the first stage is Prophase in which the chromsomes condense and centrioles move to opposite poles. And in Meiosis, the first stage is Prophase I in which the same thing occurs
