Energy is not created or destroyed due to the law of Conservation of Energy. Hope this helps!
Answer:
The same instrument must be used to measure the unknown solution as was used to measure the known (standard) solutions that were used to create the calibration curve.
The analyte in the unknown solution must be the same analyte (or type of analyte) that is present in the known (standard) solutions that were used to create the calibration curve.
Domain and range restrictions must be observed.
Explanation:
Calibration curves are tools necessary in understanding the instrumental response for any analyte.
A calibration curve is obtained by preparing a set of standard solutions with known concentrations of the analyte. The instrument response for each concentration is measured and plotted against the concentration of the standard solution. The linear portion of this plot may be used to determine the unknown concentration of a sample of the analyte.
The equation of the best-fit line is used to determine the concentration of the unknown sample.
Answer:
The α‑helix is held together by hydrogen bonds between the amide N−H and C=O groups.
Disulfide bonds stabilize secondary structure.
Explanation:
Proteins have primary, secondary, tertiary and quartinary structures.
The secondary structure of a protein is the regular, recurring sequence of amino acid in a polypeptide chain. Secondary structure of proteins give rise to the folding observed in the structure of a protein.
The major secondary structures of a protein are α-helices and β-structures.
Answer: Another name for beta-minus particle is electron.
Explanation: Beta-minus particle is released during the beta-minus decay nuclear reaction.
In this nuclear reaction, a neutron gets converted into proton and electron. The electron released is the beta-minus particle.
The charge on these particles is -1 and mass of these particles is negligible.
When a cell uses chemical energy to perform work it couples exergonic reaction with endergonic reaction.