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The process of passing the solvent through the column is called elution.
A chemical identification was made on the basis of its elution position just before Fm.
A Birch reduction of naphthalene takes 5 minutes elution time.
The time taken for a component to pass through the column is called its elution time.
Usually a gradient (to increasing amounts of water) is enough to promote elution.
For elution, a buffer with increasing phosphate concentration is typically used.
The larger the particles, the faster the elution.
The same buffer was used for protein elution and fractions of 0.5 ml were collected.
There are distinct differences between displacement and elution chromatography.
The speed at which any component of a mixture travels down the column in elution mode depends on many factors.
In conventional chromatography, separation of similar compounds can be improved by gradient elution.
First results were disappointing as no alpha-particle emission signature could be detected from the elution product.
Ga is a positron emitter, with a 68 minute half life, produced by elution from germanium-68 in a gallium-68 generator.
This resulted in successful and resolved elution of angiotensin peptides.
The final result was approximately 50 μl of nucleic acid in elution buffer.
Predicting and controlling the order of elution is a key aspect of column chromatographic methods.
Under a particular set of conditions, the amino acids will elute in the same order and at the same elution volume.
The gold can be removed from the carbon by using a strong solution of caustic soda and cyanide, a process known as elution.
The actinide elution sequence is reversed from that of the cation-exchange resin column.
Nonetheless, it has drawbacks such as low resolution, low capacity and low elution times.
In many cases, baseline separation of the peaks can be achieved only with gradient elution and low column loadings.
Any interaction leads to a later elution time and thus mimics a smaller analyte size.
During elution, excess glutathione is used to displace the tagged protein.
This is the established elution behavior of *AroQ [ 18].
They also quantified levels of Aβ-degrading activity using elution from column chromatography.