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Key Documents

DCL6B100

Sigma-Aldrich

DEAE–Sepharose

CL-6B

Synonym(s):

Diethylaminoethyl–Sepharose

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
47101511
NACRES:
NA.56

Quality Level

form

suspension

technique(s)

affinity chromatography: suitable

matrix

6% cross-linked agarose

bead size

45-165 μm

pore size

~4,000,000 Da exclusion limit

pH

3—12

capacity

130-170 μeq/mL binding capacity (gel volume)(gel volume)

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General description

DCL6B100-500ML′s updated product number is GE17-0710-01

Application

DEAE-Sepharose® is used in affinity chromatography, protein chromatography and ion exchange chromatography. DEAE-Sepharose has been used to study pathogenesis of human disease and to develop a new assay for detecting the toxins of pathogenic strains of Clostridium difficile.

Legal Information

DEAE-Sepharose is a registered trademark of Cytiva
Sepharose is a trademark of Cytiva

replaced by

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

100.4 - 109.4 °F

flash_point_c

38 - 43 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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J J Wheeler et al.
Gene therapy, 6(2), 271-281 (1999-08-06)
A detergent dialysis procedure is described which allows encapsulation of plasmid DNA within a lipid envelope, where the resulting particle is stabilized in aqueous media by the presence of a poly(ethyleneglycol) (PEG) coating. These 'stabilized plasmid-lipid particles' (SPLP) exhibit an
M A Heine et al.
Molecular biology of the cell, 4(11), 1189-1204 (1993-11-01)
Epitope-tagged Xenopus nucleolin was expressed in Escherichia coli cells and in Xenopus oocytes either as a full-length wild-type protein or as a truncation that lacked the distinctive carboxy glycine/arginine-rich (GAR) domain. Both full-length and truncated versions of nucleolin were tagged
R K Sinha et al.
Vaccine, 15(6-7), 689-699 (1997-04-01)
Six different secretory proteins of molecular weights (15, 26, 30, 41, 55 and 70 kDa) were isolated from 8-day-old culture filtrate of Mycobacterium tuberculosis H37Ra using different column chromatography techniques. These proteins were further examined for their ability to induce
I Yu Bakunina et al.
Biochemistry. Biokhimiia, 67(6), 689-695 (2002-07-20)
An alpha-N-acetylgalactosaminidase IV able to remove blood type specificity of human A(II)-erythrocytes and not effecting B(III)-erythrocytes was isolated from the marine bacterium Arenibacter latericius KMM 426T. The alpha-N-acetylgalactosaminidase IV preparation exhibits high activity during inhibition of hemagglutination with blood group
M L Zapp et al.
Proceedings of the National Academy of Sciences of the United States of America, 88(17), 7734-7738 (1991-09-01)
The Rev protein of human immunodeficiency virus type 1 is a sequence-specific RNA binding protein that is essential for viral replication. Here we present evidence that Rev is a stable oligomer both in vitro and in vivo. Analysis of Rev

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