Answer:
No
Explanation:
Mitosis is the process in cell division where the nucleus divides into two nuclei, each with an identical set of chromosomes. Mitosis is divided into four phases: prophase, metaphase, anaphase, and telophase. The shortest stage of the cell cycle is called cytokinesis (division of the cytoplasm).
There should be options for this question.
They are:
A. By plan type
B. By determining the last plan inactivated
C. By the order they were entered
D. By the BIN.
The correct answer is A. By plan type.
The computer system groups together multiple plans for one patient and organizes them by plan type. Therefore when a medical professional goes to look at the patient pharmacy record they can see each specific plan type for the patient in order.
Answer:
Studies have been conducted on synthetic products, including DDT and estrogen. The use of these synthetic products has been discontinued due to increased risk of cancer and other health concerns. Genetic engineering has increasingly been used in cattle, crops, and pharmaceuticals.
Explanation:
Answer/Explanation:
(1) a mutation in the coding region, resulting in an inactive protein
To check to see if there is a mutation, you could extract the DNA from the cancer cells and then perform PCR to amplify the gene of interest. You could then perform sanger sequencing and compare the sequence to the normal gene to see if a mutation is present. To test the effect of the mutation, you would want to see if an active protein has been formed.
To see if a normal sized protein has been formed, you could perform a western blot, comparing the protein band to the WT protein band. If the protein is absent or much smaller, it is likely not a functional protein.
(2) epigenetic silencing at the promoter of the gene, resulting in reduced transcription.
To check for changes in the epigenetic landscape of the promoter, you could perform chromatin immunoprecipitation by extracting the chromatin from the tumour cells and using antibodies for different chromatin marks to see what has changed between the normal cells and the tumor cells. E.g. H3K9me3, H3K27me3. You would perform a pull down with the antibody of interest and then PCR for your promoter to specifically look at changes at that gene compared to normal cells. To test DNA methylation, you could perform bisulfite sequencing.
To see how transcription is affected, you could extract RNA from the tumor and normal cells, and compare the levels of RNA between the two samples by qRT-PCR
