More than one of the species may contribute to the absorbance.

It is necessary to know how quickly the absorbance changes with concentration.

In this case, the greater the absorbance, the higher the protein concentration.

In many cases, an absorbance band is present in only one form.

Absorbance readings were measured at 405nm after 20 minutes.

These often possess many absorbance bands and are unique for each ring structure.

This amount is based on the progress, outcome and absorbance of LA2.

Detailed photographic data of each towel structure and its comparison to absorbance is important information.

Any real measuring instrument has a limited range over which it can accurately measure absorbance.

The deviations will be most noticeable under conditions of low concentration and high absorbance.

The graph normalizes the degree of absorbance on a hundred point scale.

The detergents will cause a swelling effect which could be measured by an absorbance change.

This positive absorbance difference is indicative of O intermediate formation.

This shift in absorbance is apparent to the human eye as a slightly more greenish colour.

Plot the absorbance of the standards vs. their concentration.

Instrument - deviations which occur due to how the absorbance measurements are made.

Then, using a spectrophotometer, they were able to measure the light absorbance of the pigments.

The absorbance of the filtrate was measured at 600 nm.

This causes an increase in the absorbance at 595 nm independent of protein presence.

It measures the absorbance of different wavelengths of light in a solution.

MMP activity was represented by the change of absorbance over time.

Stop solution was added after blue colour development, and the absorbance was read at 450 nm.

Absorbance measurements are often carried out in analytical chemistry.

The concentration is determined by measuring the absorbance of this gas at 253.7 nm.

The opposite, a decrease of absorbance is called hypochromicity.