I believe that the most common antibody switch is from IgM to IgG.
Class switching occurs by a mechanism called the class switch recombination binding. It is a biological mechanism that allows the class of antibody produced by an activated B cell to change during a process known as isotype or class switching. The mechanism changes a B cell's production of antibodies from one form to another, such as from the isotype IgM to the isotype IgG.
The answer is B. Digestive and cardiovascular
<span>It will have little impact in the long run. Muscular dystrophy tends to interfere with the formation of muscular tissue, specifically it causes problems with the manufacturing of proteins necessary to maintain muscular tissue. This procedure would mean a temporary improvement in the subjects condition, but does not seem to provide a true permanent solution. Repetitive stem cell therapy may be able to slow down the conditions progression though.</span>
It would grow about 3-5 inches per year.
Answer:
PFFT this might help? sorry if not mate
Explanation:
Cell cycle checkpoint controls play a major role in preventing the development of cancer [see Sherr, 1994, for a more detailed discussion]. Major checkpoints occur at the G1 to S phase transition and at the G2 to M phase transitions. Cancer is a genetic disease that arises from defects in growth-promoting oncogenes and growth-suppressing tumor suppressor genes. The p53 tumor suppressor protein plays a role in both the G1/S phase and G2/M phase checkpoints. The mechanism for this activity at the G1/S phase checkpoint is well understood, but its mechanism of action at the G2/M phase checkpoint remains to be elucidated. The p53 protein is thought to prevent chromosomal replication specifically during the cell cycle if DNA damage is present. In addition, p53 can induce a type of programmed cell death, or apoptosis, under certain circumstances. The general goal of p53 appears to be the prevention of cell propagation if mutations are present. The p53 protein acts as a transcription factor by binding to certain specific genes and regulating their expression. One of these, WAF1 or Cip1, is activated by p53 and is an essential downstream mediator of p53-dependent G1/S phase checkpoint control. The function of p53 can be suppressed by another gene, MDM2, which is overexpressed in certain tumorigenic mouse cells and binds to p53 protein, thus inhibiting its transcriptional activation function. Other cellular proteins have been found to bind to p53, but the significance of the associations is not completely understood in all cases. The large number of human cancers in which the p53 gene is altered makes this gene a good candidate for cancer screening approaches.
