Examples of 'superdex' in a sentence
Meaning of "superdex"
superdex (noun): A brand name for a range of size-exclusion chromatography resins used for protein purification and biomolecule analysis in biochemistry and biotechnology laboratories
How to use "superdex" in a sentence
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superdex
It was further purified by gel filtration on a Superdex peptide column.
Superdex separation was carried out in PBS.
By means of size chromatography Superdex 75 a small portion of the xylanase has been highly purified.
Coli western blot indicated HCP contamination below 1 % in the Q eluate and in the Superdex eluate.
A step of size exclusion chromatography using Superdex 75 was therefore added to the purification process.
A size exclusion chromatography resin such as Superdex 75.
The technical details of the Superdex 75 pg matrix are as follows,.
Preferably the packing material employed is Superdex 75pg.
All VHs were subjected to Superdex 75 gel filtration chromatography.
The extract is then fractionated by exclusion chromatography on a Superdex 75 column ( Pharmacia ).
In some embodiments, Superdex 75 size exclusion chromatography is used in the purification of DsbC.
The concentrate was divided into two separate loads for the Superdex 75.
Further purification was completed by Superdex 200 prep grade size exclusion column.
The composition of matter of claim 1 wherein the size exlusion chromatography resin is Superdex 200pg.
Final purification was completed by Superdex 200 prep grade size exclusion column.
See also
Figure 5 shows a graph of purification of human placental bikunin from placental tissue after Superdex 75 Gel-Filtration.
The fraction was then loaded onto a Superdex 75 ( size exclusion chromatography ) column equilibrated in PBS.
The Superdex 200 column separated the smaller starting materials from the conjugates based on molecular size.
As the final step, gel filtration is carried out through Superdex 75 under alkaline conditions.
Calibration curve of the Superdex 200 column based on retention volumes of the indicated proteins.
The inhibition of the various fractions eluted from the superdex column as shown in Fig . 19.
Superdex The pooled Phenyl Sepharose fractions are then subjected to size exclusion chromatography, using Superdex 75.
The KLH-IFNa preparation is passed on a superdex S200 column following the above described conditions.
An aliquot of the purified material was analysed on a Superdex 200HR column.
Proteins were then loaded onto a Superdex 75 ( GE Healthcare ) column for final purification.
The molecular weight distribution was measured by GPC on Superdex 200.
Detection by UV 214 nm absorbance and the Superdex column calibrated by dextran Mw standards.
Superdex 75 is especially preferred.
The fractions containing LPP < srSHe were loaded on a Superdex 75 column.
A preferred column is a Superdex 200 size exclusion medium.
Chromatographic separation of the concanavalin A using a Superdex 200 column.
VIs were subjected to Superdex 75 gel filtration chromatography at a concentration of 0.6 mg / ml.
The size exclusion chromatography was performed using Superdex 75 pg, available from GE Healthcare.
Lane 3 depicts the electrophoretic pattern of the SERP-1 protein further purified to homogeneity by Superdex 75.
The SH2 domain was further purified to homogeneity using Superdex 75 gel filtration chromatography.
Superdex 200 ( Pharmacia ) was used for this, and a conventional process of gel filtration in a HPLC equipment.
Peptide size analysis was carried out by chromatography over a Superdex Peptide HR 1030 column.
Superdex Peptide chromatogram of 2-AB derivatized saccharide fraction analyzed at 336 nm.
The eluted integrase protein solution was applied to a Superdex 75 ( Pharmacia Corporation ) column for gel filtration.
A method according to claim 8, wherein said stationary phase is Superdex 75.
The reaction solution was treated with a Superdex peptide column 16 mm ID x 30 cm, mfd.
The Superdex 75 column fractions were tested for binding to KIT225 cells by FACS analysis.
The sample was applied to a Superdex 200 column.
SEC was performed on a Superdex 200 column using an Äkta chromatography system ( GE-Healthcare ).
A size exlusion chromatography resin such as Superdex 200pg.
Size exclusion chromatography on Superdex 200 ™ ( GE Healthcare ) was used as second purification step.
The fractions containing SHe-tGCN4 were loaded on a Superdex 75 column.
HPLC chromatography of the Superdex 200 pool indicated that indeed His34 was the major PEGylation site.
Caspase-14 was subjected to final purification using Superdex 75 gel chromatography.
Figure 5 is a graph of a Superdex G75 gel filtration of recombinant KAAG1 sample.
