Answer:
B.) Carbon and Hydrogen
Explanation:
Lactose is a carbohydrate, and carbohydrates are primarily made of carbon and hydrogen chains.
Hey all I gotta say is look up the definition and you’ll find the answers it’s not that complicated
<span>The balanced equation for ammonia (NH3) is 3H2 + N2 ď 2NH3. This equation starts from H2 + N2 ď NH3. We have 1 N and 3 H on the right side (the product side) of the equation, so we multiply each by 2 to get 2 N and 6 H. We do this so that we don’t have an odd number of H atoms. We then balance the left side (the reactant side) of the equation with the right side, N is already balanced, but we have to multiply H by 3 to get 6 H atoms (to match the right side of the equation.</span>
Answer:
After this treatment, the investigators should expect to get a mixture of the desired enzyme, plus fragments of the peptide used to desorb the enzyme in question.
This would be the result of using a peptide as a desorption solution when the desired protein is a protease,
Assuming that the protease retains its activity in the medium in question, and that the peptide can act as a substrate (which would make sense), as the peptide solution is added, it will interact with and bind to the antibody, but some molecules will also interact with the active site of the enzyme as it desorbs and passes through, culminating on the elution of the hydrolized part of the peptide along with the enzyme.
Answer and explanation;
The hydrophobic effect is the observed tendency of non-polar substances to aggregate in an aqueous solution and exclude water molecules. Hydrophobic interaction is mostly an entropic effect originating from the disruption of highly dynamic hydrogen bonds between molecules of liquid water by the non-polar solute.
Introduction of such a non-hydrogen bonding surface into water causes disruption of the hydrogen bonding network between water molecules.
Water dissolves molecules (proteins and nucleic acids) that display on their solvent-accessible surfaces groups that can h-bond [hydroxyl, carbonyl, ester groups; they're polar uncharged...also charged groups; protonated amines, carboxylates and phosphate ethers.
Molecules with internal h-bonds dissolve in water, some/all internal h-bonds may be in dynamic exchange with h-bonds in water
.
Polar nature of water contributes to ability to dissolve non-ionic polar organic molecules, such as phenols, esters, amides; have large dipole moments and interaction with water dipole promotes solubility in water.
