chromatographic
chromatographical

Then a purification in one chromatographic step is not possible.

There is little if any sample preparation and no chromatographic separation.

Both chromatographic methods thus consist essentially of two steps: 1.

Relative to chromatographic methods, large amounts of material are required.

The distribution is used as a theoretical model for the shape of chromatographic peaks.

The gas chromatographic determinative steps are found in Methods 8015 and 8021.

However, chromatographic techniques can easily distinguish and measure each of these substances.

The real chromatographic analysis starts with the introduction of the sample onto the column.

However, chromatographic methods for separation started being adopted in the early 1980s.

If two values are not separated, it still indicates some uniformity of chromatographic system.

The particles are detected at the outlet with a standard chromatographic detector.

Usually a protein purification protocol contains one or more chromatographic steps.

Chromatographic processes began to take shape in 1983.

Its large size and planarity have also shown promise as a chromatographic separation material.

All of the chromatographic techniques require a calibration step prior to sample analysis.

Production is chiefly through chromatographic separation, using techniques such as the "simulated moving bed".

A common application for the material is in chromatographic separations of biomolecules.

Another approach to study particle deposition is to investigate their transport in a chromatographic column.

Chromatographic techniques have been used in blood processing and purification since the 1980s.

Although it was hard to make chromatographic processing methods widely adopted, global expansion is a work in progress.

Monitoring of the drug in plasma or serum is generally accomplished using chromatographic methods.

More conventionally, the detectors are coupled to a variety of different chromatographic separation systems.

The width of the injected plug should be small compared to the spreading due to the chromatographic process.

Since that time, chromatographic techniques have advanced significantly.

After one hour samples of the bile were taken for nucleation studies and chromatographic separation.

Ion exchange chromatography is a chromatographical method that is widely used for chemical analysis and separation of ions.

However, a more recent study in bovine brain suggested the existence of multiple N-SMase isoforms with different biochemical and chromatographical properties.

Chromatographical separation, in addition to the antibiotics pyrromycin and cinerubin A and B, reveals several individual components of bohemic acid, including alcindoromycin, bohemamine, collinemycin, marcellomycin, mimimycin, musettamycin, rudolphomycin and schaunardimycin.