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S4027

Sigma-Aldrich

Sulfoxyethyl cellulose Fast Flow

fibers

Synonym(s):

Sulfoxyethyl cellulose

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About This Item

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

form

fibers

Quality Level

Application

Sulfoxyethyl cellulose is used in protein chromatography, ion exchange chromatography and cation exchange media. Sulfoxyethyl cellulose has been used to purify and characterize a phosphatidylinositol transfer protein from human platelets and to purify an acid DNase (DNase II) from porcine spleen.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The Arabidopsis genome contains 17 predicted beta-galactosidase genes, all of which belong to glycosyl hydrolase (GH) Family 35. These genes have been further grouped into seven subfamilies based on sequence similarity. The largest of these, subfamily a1, consists of six
D Wong et al.
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Previous studies have shown that sulfate-reduction activity occurs in a heterogeneous manner throughout the terrestrial subsurface. Low-activity regions are often observed in the presence of clay minerals. Here we report that clays inhibit sulfate reduction activity in sediments and in
X Zeng et al.
Biotechnology progress, 15(6), 1003-1019 (1999-12-10)
As a result of the convective flow of solutes through porous membranes, membrane chromatography has a higher capture efficiency and a higher productivity than column chromatography and shows most promising industrial applications for the recovery, isolation, and purification of proteins
J Hall et al.
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The reaction of Rhodobacter sphaeroides cytochrome c2 with the Rb. sphaeroides cytochrome bc1 complex was studied by using singly labeled cytochrome c2 derivatives. Cytochrome c2 was treated with chlorodinitrobenzoic acid to modify lysine amino groups to negatively charged carboxydinitrophenyllysines and

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