From what I remember it's called a substrate
I believe using gel electrophoresis to separate and identify plasmids and short linear pieces of DNA would be important if one is making a recombinant plasmid and has to verify that he/she has been successful. Gel electrophoresis is a technique that is used to separate mixtures of DNA, RNA, or proteins according to molecular size. The molecules being separated are pushed by an electrical field through a gel that contains small pores.
B. Bacteria and Archaea, both are Prokaryote cells
Answer:
D. The methyl group of acetyl CoA becomes radio-labeled
Explanation:
During the steps in glycolysis, the carbon at position 1, becomes C-1 in dihydroxyacetone phosphate during the cleavage of fructose-1,6-bisphosphate to dihydroxyacetone phosphate and glyceraldehyde-3-phosphate. Subsequently on isomerization of dihydroxyacetone phosphate to glyceraldehyde-3-phosphate, C-1 of dihydroxyacetone phosphate becomes C-3 of glyceraldehyde-3-phosphate.
Furthermore, in pyruvate, the end product of glycolysis, C-3 is converted to a methyl group which then becomes the methyl group in the acetyl-CoA molecule produced from the oxidative decarboxylation of pyruvate.
Since the radioactive 14-C of radio-labeled glucose occupies position 1, it will become the methyl group of acetyl-CoA.
Acidosis probably has something to do with acid in the blood, and the injection will probably balance out the acidosis.
