elution's Usage Examples:

In analytical and organic chemistry, elution is the process of extracting one material from another by washing with a solvent; as in washing of loaded.

constant ("isocratic elution mode") or varied ("gradient elution mode") during the chromatographic analysis.

Isocratic elution is typically effective.

desorbed by an elution buffer.

The mode used for elution (expanded-bed versus settled-bed) depends on the characteristics of the feed.

After elution, the adsorbent.

who in 1943 first classified the modes of chromatography as frontal, elution, and displacement.

This type of elution is called gradient elution.

On the other hand, step elution can be used in which the concentration of.

developed between 24 hours and 28 days after cessation of transfusion Positive elution test with alloantibodies present on the transfused red blood cells OR newly.

incomplete recovery of the analytes by SPE caused by incomplete extraction or elution.

Target biomolecules may then be removed by applying a so-called elution buffer, which disrupts interactions between the bound target biomolecules.

To determine approximate molecular weight, the elution volumes of compounds with their corresponding molecular weights are obtained.

elutes very late in the elution sequence, after fermium.

Another method to isolate mendelevium exploits the distinct elution properties of Md2+ from those.

by gradient elution.

In MEKC, however, techniques must be used to extend the elution range to separate strongly retained analytes.

the result of the first application of rate theory to the chromatography elution process.

Kleihauer–Betke ("KB") test, Kleihauer–Betke ("KB") stain, Kleihauer test or acid elution test, is a blood test used to measure the amount of fetal hemoglobin transferred.

In place of solvent gradient elution, thermoresponsive polymers allow the use of temperature gradients under.

prepare for subsequent rounds of selection in which the stringency of the elution conditions can be increased to identify the tightest-binding sequences.

The filter paper based lysis and elution method features high throughput capacity.

An elution with a low pH buffer or a more gentle, high salt elution buffer is then used to recover purified antibody.

imidazole enables elution from Ni-NTA, whereas for proteins with two hexahistidine tags, 100 mM imidazole is required for elution.

EGTA is used as a compound in elution buffer in the protein purification technique known as tandem affinity purification.

buffer) but become dissociated and return to solution in buffer B (the elution buffer).

Synonyms:

extraction;