Answer:
The correct answer is option (C) "After splitting ATP, a protein changes shape to pump ions across a membrane".
Explanation:
Adenosine triphosphate (ATP) is an organic chemical molecule considered the "molecular unit of currency" of intracellular energy transfer, for the high level of energy that is released when ATP is breakdown into adenosine diphosphate (ADP). ATP provides energy to drive many processes in living cells. One example of how the chemical potential energy of this molecule is turned into work is that after splitting ATP, a protein changes shape to pump ions across a membrane. The energy of the splitting of ATP into ADP will provide energy for the protein being able to change shape, resulting in pumping ions across a membrane.
the region of a chromosome to which the microtubules of the spindle attach, via the kinetochore, during cell division.
Brainliest Please :)
Compare and contrast two mechanisms for transcriptional termination in bacteria.
(rho)p-dependent termination: requires rut (rho utilization site), rho protein binds, moves towards 3' end, DNA encodes GC rich for stem loop, RNApoly pauses, rho protein catches up and separates RNA-DNA hybrid
(rho)p-independent termination: Uracil-rich sequence causes RNApoly to pause, stabilized by NusA near open complex RNA exit, UA bonds to weak to hold, DNA-RNA hybrid dissociates AKA intrinsic termination
hope this help
Answer: Option A.
Transverse tubules rapidly move the action potential to the interior of the muscle potential.
Explanation:
Transverse tubules are cylindrical pockets found in the plasma membrane of muscle cells. They are formed from phospholipid bilayer or sarcolemma of skeletal or cardiac muscle cells. They have membrane that have large concentration of ion channels,transporters and pump. They permit action potention into the cell and also to a particular structure sarcuplasmic reticulum. They play a role in regulating cellular calcium concentration.
Answer:
C.The added epitope disrupts the function of the tagged protein
Explanation:
When an additional sequence is tagged to a protein to use comercial antibodies, there are several reasons why this procedure wouldn't work as expected (note that we're assuming the protein is being expressed but it's not possible to detect it).
For example, the sequence of nucleotide added to codify for the tagged epitope are removed during the RNA processing. In that case, the protein would be expressed without the epitope, so it would be impossible to localize it with the antibodies.
Also, it could be that the new epitope is affecting some way the protein folding, making it not functional. This way, it would be degraded by the cell so it wouldn't be detected.
Another possibility is that the epitope doesn't affects the protein folding nor its function, but during the folding ends up in a conformation that makes it inaccesible for the antibody.
In summary, the way as the possible answers to this question are shown, the correct option seems to be C:<em> The added epitope disrupts the function of the target protein.</em>
