推荐产品
形式
fibers
质量水平
应用
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.
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
D Wong et al.
Microbial ecology, 47(1), 80-86 (2004-07-21)
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
Dashzeveg Gantulga et al.
Phytochemistry, 70(17-18), 1999-2009 (2009-09-22)
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
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
P Y George et al.
Biochimica et biophysica acta, 836(2), 176-184 (1985-09-11)
We report the purification of a phospholipid transfer protein from human platelets. This protein preferentially transfers phosphatidylinositol, with phosphatidylcholine and phosphatidylglycerol being transferred to a lesser extent. Phosphatidylethanolamine is not transferred. Transfer activity is detected by measuring the transfer of
J Hall et al.
Biochemistry, 28(6), 2568-2571 (1989-03-21)
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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