Mitosis is nuclear division. During Mitosis, chromosomes that have already been duplicated, attach to spindle fibers that pull a copy of each chromosome to the opposite side of the cell.
Pretty much creating 2 daughter nuclei
Answer:
b. Sufficient concentration and correct orientation of particles
Explanation:
Collision theory states that when two suitable particles states that when suitable particles of the reactant collide with other and causes any noticeable chemical change, these successful changes are called collisions.
<em>Two factors that responsible for collision are reactant concentration and correct orientation of particles. </em>
<u>Reactant concentration:</u><u> </u>higher concentration of reaction will increase the rate of reaction as, it will provide more reactant to collide in a specific time period.
<u>Orientation of particles:</u> the correct orientation of particles facilitate the forming and breaking of bonds and arrange the atoms to form product molecules.
Hence, the correct option is "Sufficient concentration and correct orientation of particles "
Answer:
False
Explanation:
Toxoplasma is a congenital disease that is characterized by mild muscle aches, tender lymph nodes, etc. and in some immuno-compromised individuals, seizures and coordination loss may occur. I
The disease is caused by a protozoan known as <em>Toxoplasma gondii </em>and its infection is usually by eating foods (usually meats) that contain the cyst of the organism or making contact with cats that are infected in addition to infected mother-baby transmission, especially during pregnancy.
<em>Hence, humans can contract the organism not just by exposure to an infected cat but also by eating meats that contain the cysts of the organism.</em>
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
.
Answer #1: instinctual trait
Answer#2: learned trait
