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Merck
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Key Documents

S6657

Sigma-Aldrich

Superdex®

Superdex®75 Prep Grade

Sinónimos:

Superdex Resin

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About This Item

MDL number:
UNSPSC Code:
23151817
NACRES:
NA.56

form

suspension (20% aqueous ethanol)

technique(s)

protein array: suitable

matrix

cross-linked agarose

particle size

24-44 μm

pore size

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

operating pH range

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

storage temp.

2-8°C

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General description

Combina la elevada selectividad de una matriz Sefadex con la estabilidad física y química de la agarosa reticulada.

Application

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.
Optimizada para separaciones preparativas para alta resolución.

Legal Information

Superdex is a registered trademark of Cytiva

Pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

104.0 °F

flash_point_c

40 °C


Certificados de análisis (COA)

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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
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
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
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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