推荐产品
质量水平
表单
suspension
技术
affinity chromatography: suitable
基质
6% cross-linked agarose
珠子尺寸
45-165 μm
孔径
~4,000,000 Da exclusion limit
pH值（酸碱度）
3—12
容量
130-170 μeq/mL binding capacity (gel volume)(gel volume)
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一般描述
DCL6B100-500 mL 更新后的产品编号为 GE17-0710-01
应用
DEAE-Sepharose ® 用于亲和层析、蛋白层析和离子交换层析。DEAE-Sepharose ™ 已被用于研究人类疾病的发病机制和开发检测艰难梭菌致病菌株毒素的新方法 。
法律信息
DEAE-Sepharose is a registered trademark of Cytiva
Sepharose is a trademark of Cytiva
警示用语：
Warning
危险声明
危险分类
Flam. Liq. 3
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
100.4 - 109.4 °F
闪点(°C)
38 - 43 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
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
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
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
Preparative affinity precipitation of L-lactate dehydrogenase.
Pearson, J.C., et al.
Journal of Biotechnology, 11(2-3), 267-274 (1989)
I A Oussenko et al.
Journal of bacteriology, 182(9), 2639-2642 (2000-04-13)
Studies of Bacillus subtilis RNases that are involved in mRNA degradation reveal a different pattern from that of Escherichia coli. A strain lacking polynucleotide phosphorylase, the major 3'-to-5' exoribonuclease activity in cell extracts, is viable. Here, we show that the
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