Examples of 'sepharose' in a sentence
Meaning of "sepharose"
Sepharose is a verb that does not have a widely recognized definition in the English language. It may be a specialized term in a specific field or a typo
Show more definitions
- A cross-linked polysaccharide bead-formed gel based on agarose.
- Alternative form of Sepharose
How to use "sepharose" in a sentence
Basic
Advanced
sepharose
In one embodiment the solid support is sepharose.
Sepharose has been found to be suitable for this purpose.
Enzyme was purified by means of a glutathione sepharose column.
Sepharose beads were removed from the supernatants by centrifugation.
The chromatography columns may be sepharose based.
Q sepharose chromatography was then used to remove short saccharide fragments.
Biotinylated product is bound streptavidin sepharose beads.
Control samples containing sepharose beads not conjugated to novobiocin are done in parallel.
Said solid support may be sepharose.
Sepharose may be used.
An example of such a preferred material is cysteine or glutathione immobilised to sepharose.
Sepharose beads are added at a concentration at which essentially all antibodies are captured.
The mixture was applied onto the phenyl sepharose column.
The sepharose gel was washed with distilled water until neutral on a glass filter.
The library may be immobilized on for example sepharose or agarose beads.
See also
Sepharose beads can be used when the assay is performed with a washing step.
Receptors were purified from the supernatant by affinity chromatography on glutathione sepharose.
It was surprising that linking the ligand to sepharose leads to superior results.
Concentration of staphylococcal enterotoxin from food extract using copper chelate sepharose.
The sophorolipidis are biosurfactants composed of a sepharose linked to a chain hydroxy fatty acid.
The domains were separated from each other by affinity chromatography on heparin sepharose.
Amount of sepharose.
The proteins were purified by affinity chromatography using glutathione sepharose beads.
Further fractionation was carried out on a sepharose column which separates according to molecular size.
In an even more preferred embodiment of the present invention said solid support is sepharose.
The anx sepharose ff column and the citrate buffer showed better protein separation profile.
The hydrophobic interaction chromatography of step b is preferably using a butyl sepharose chromatography resin.
The regenerated Sepharose was much lighter in colour.
The fusión protein from the culture media was purified to homogeneity on IgG sepharose chromatography.
TEA immobilized on sepharose gel was used as the inhibitor.
Lactoferrin is removed using a heparin Sepharose support.
On phenyl Sepharose chromatography the hydrogenase exhibited hydrophobic properties.
The appropriate hydrophobic substance preferably comprises phenyl Sepharose.
Phenyl sepharose HP has a strong hydrophobic property and excellent purification capability.
A convenient chromatographic procedure includes chromatography on lactose Sepharose gels.
The Sepharose resin with attached human IgA is poured into a column.
The protein of the invention is digested by trypsin bound to Sepharose.
Methidium dyes have been attached to sepharose particles to provide a DNA isolation product.
The AB antigen used in these affinity measurements was attached to sepharose beads.
The Sepharose resin with attached human IgG is poured into a column.
Any size exclusion matrix such as Sepharose may be used.
Before regeneration the Sepharose has a brown colour indicating deposited material on the gel.
The resulting lectin was purified by affinity on lactose Sepharose or asialofetuin columns.
The Phenyl Sepharose step was performed at room temperature.
The elastase digestion mixture was applied onto a lysine Sepharose column.
The supernatant is filtered through Sepharose which allows proteins termed soluble to be isolated.
Recombinant human PPAR receptors were purified by affinity chromatography on glutathione sepharose.
Pure mAbs are prepared by protein A sepharose purification of IgG from hybridoma culture supernatants.
Then the Dynal bead mixture was added to the resuspended sepharose beads.
Phenyl sepharose HP is preferred.
