The process of dissolving two organic molecules in a polymer and recombining the water molecules to create new monomers is known as hydrolysis.
<h3>What is hydrolysis?</h3>
The molecule is broken in a hydrolysis reaction involving an ester bond, such as the one between two amino acids in a protein. As a result, the water molecule (H₂O) splits into two groups: one that forms a hydroxyl (OH) group with the remaining hydrogen proton (H+) and another that transforms into a carboxylic acid.
Practically speaking, hydrolysis refers to the process of separating compounds when water is present.
Condensation, which is the process by which two molecules combine to produce one bigger molecule, can also be thought of as the opposite reaction to hydrolysis. The outcome of this reaction is that a water molecule is ejected by the larger molecule.
The three primary hydrolysis processes are
- Acid hydrolysis.
- Base hydrolysis.
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I believe it is idiopathic.
Performing a cut (also known as earthmoving)
Answer:
4 ul Loading Buffer + 19.70 ul dH2O + 0.30 ul DNA Ladder
Load 12 ul on the gel.
Explanation:
DNA Ladder concentration = 1000 ug/ml
1000 ug DNA in 1 ml DNA Ladder solution → 150 ng DNA = 0.15 ug DNA in..... 0.00015 ml = 0.15 ul DNA Ladder solution
6x DNA Loading Buffer → it has to be diluted by an equal volume 6 times (1 ul LB + 1 ul distilled H2O)
An appropriate volume to load on an average agarose gel is 12 ul, so:
2 ul Loading Buffer + 9.85 ul dH2O + 0.15 ul DNA Ladder = 12 ul
But since 0.15 ul is a very small volume and mistakes could be made while measuring it, let's make double:
4 ul Loading Buffer + 19.70 ul dH2O + 0.30 ul DNA Ladder = 24 ul
And load half of that solution (12 ul) on the gel.
Answer:
Nucleic acids have the most control of traits and inheritance.
