Answer:
a. water into root hair cells
Explanation:
Osmosis can be defined as a process which typically involves the movement of a solvent molecule such as water through a semi-permeable from a region of high concentration to a region of lower concentration.
Hence, the process of osmosis is best illustrated by the movement of water into root hair cells because they are used by the plants to absorb water from the soil.
Answer:
im not suuuuureeeeeeeee but i think its a
Answer: False
Explanation: The COMPLEMENT SYSTEM consists of proteins synthesized in the liver. They are activated by inespecific harmful substance (antigen) and begins a cascade of proteins that finally forms an attack complex against bacteria.
The COMPLEMENT is part of the INNATE IMMUNITY, because it is an inherent response, something all humans born with, and it is part of the first defense barrier against any antigen. Part of the innate immunity are too: natural killer cells, neutrophils, monocytes, dendritic cells and macrophages.
On the other hand, the ADAPTATIVE IMMUNITY, is the response that the body develops after being exposed to an antigen before. It is like something that the body recognizes, and then "learns" how to act against it. Part of the adaptative immunity are: lymphocyte T and B, and the antibodies (substances called Immunoglobulins). The immunoglobulins (Ig) are glycoproteins present in the blood.
Answer:
It will determine the number of molecules of the particular chemical in the compound.
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
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