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Merck

S6657

Sigma-Aldrich

Superdex®

Superdex®75 Prep Grade

Synonym(e):

Superdex Resin

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About This Item

MDL-Nummer:
UNSPSC-Code:
23151817
NACRES:
NA.56

Form

suspension (20% aqueous ethanol)

Methode(n)

protein array: suitable

Matrix

cross-linked agarose

Partikelgröße

24-44 μm

Porengröße

3-70 kDa MW range (proteins)
500-30,000 Da MW range (dextrans)

operating pH range

1-14(short term)
3-12(long term)

Lagertemp.

2-8°C

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Allgemeine Beschreibung

Vereint die hohe Selektivität einer Sephadex-Matrix mit der chemischen und physikalischen Stabilität der vernetzten Agarose.

Anwendung

Superdex® is used for protein chromatography, gel filtration chromatography, gel filtration media, resins and separation media. Superdex® has been used for the purification and characterization of a novel laccase from the edible mushroom Hericium coralloides. Superdex® has also been used for the purification and mechanism exploration of a potential human hepatocellular carcinoma inhibitor from Bauhinia purpurea L. seeds.
Optimiert für hochauflösende präparative Trennungen.

Rechtliche Hinweise

Superdex is a registered trademark of Cytiva

Piktogramme

Flame

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

104.0 °F

Flammpunkt (°C)

40 °C


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Toshiro Matsunaga et al.
Plant physiology, 134(1), 339-351 (2003-12-13)
Borate ester cross-linking of the cell wall pectic polysaccharide rhamnogalacturonan II (RG-II) is required for the growth and development of angiosperms and gymnosperms. Here, we report that the amounts of borate cross-linked RG-II present in the sporophyte primary walls of
M Belew et al.
Journal of chromatography. A, 679(1), 67-83 (1994-09-09)
Recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF), produced as inclusion bodies in genetically transformed Escherichia coli cells was purified to homogeneity by a three-step chromatographic procedure involving hydrophobic interaction, ion exchange and gel filtration. Each purification step is reproducible and well
Cornelia Steinhauer et al.
Proteomics, 6(15), 4227-4234 (2006-07-11)
Antibody-based microarray is a novel technology with great promise in biomedicine that will provide unique means to perform global proteome analysis. In the process of designing the high-density antibody microarrays required, several critical key issues have been identified that remain
Xindu Geng et al.
Journal of biotechnology, 113(1-3), 137-149 (2004-09-24)
A new technology for renaturation with simultaneous purification of the recombinant human interferon-gamma (rhIFN-gamma) in downstream of biotechnology is presented. The strategies to develop the new technology in industry scale were suggested. Based on chemical equilibrium and molecular interactions, the
S Gibert et al.
Journal of chromatography. B, Biomedical sciences and applications, 737(1-2), 143-150 (2000-02-19)
A kinesin gene has been cloned by RT-PCR (reverse transcription polymerase chain reaction) from Trypanosoma brucei and the corresponding protein overexpressed as a recombinant His-tag (histidine-tag) kinesin in E. coli in order to study its biochemical properties and to determine

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