Answer:
d. this is one part of the cell cycle.
Explanation:
Answer:
The options are missing, the options are:
A) prevents the duplication of centrosomes. B) prevents nuclear envelope fragmentation C) prevents shortening of microtubules. D) prevents attachment of the microtubules to the kinetochore. E) prevents nucleosome formation
The answer is C
Explanation:
Cell division is a characteristics of all living cells. Whether meiosis or mitosis, the chromosomes separate in the Anaphase stage. Prior to the anaphase stage is the metaphase, where spindle microtubules attach to the kinetochores of each chromosome and aligns them at the centre of the cell called METAPHASE PLATE.
Thus, since the aligning of chromosomes at the metaphase plate has to do with attachment of microtubules to chromosomes' kinetochores, the drug that will hinder movement of chromosomes to opposite poles will not stop formation of microtubules. Instead, it will prevent the formed microtubules attached to each chromosome from shortening, as it is the shortening of microtubules that facilitates the pulling apart of the chromosomes they are attached to.
Answer:
Having considered how an appropriate primary immune response is mounted to pathogens in both the peripheral lymphoid system and the mucosa-associated lymphoid tissues, we now turn to immunological memory, which is a feature of both compartments. Perhaps the most important consequence of an adaptive immune response is the establishment of a state of immunological memory. Immunological memory is the ability of the immune system to respond more rapidly and effectively to pathogens that have been encountered previously, and reflects the preexistence of a clonally expanded population of antigen-specific lymphocytes. Memory responses, which are called secondary, tertiary, and so on, depending on the number of exposures to antigen, also differ qualitatively from primary responses. This is particularly clear in the case of the antibody response, where the characteristics of antibodies produced in secondary and subsequent responses are distinct from those produced in the primary response to the same antigen. Memory T-cell responses have been harder to study, but can also be distinguished from the responses of naive or effector T cells. The principal focus of this section will be the altered character of memory responses, although we will also discuss emerging explanations of how immunological memory persists after exposure to antigen. A long-standing debate about whether specific memory is maintained by distinct populations of long-lived memory cells that can persist without residual antigen, or by lymphocytes that are under perpetual stimulation by residual antigen, appears to have been settled in favor of the former hypothesis.
A quadrant streak is the answer
