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Merck
CN

DFF100

Sigma-Aldrich

DEAE - 琼脂糖凝胶

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别名:

二乙氨乙基 - 琼脂糖凝胶

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About This Item

CAS号:
MDL编号:
UNSPSC代码:
47101511
NACRES:
NA.56

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 (wet)

孔径

~4,000,000 Da exclusion limit

pH值(酸碱度)

2—12

容量

110-160 μeq/mL binding capacity(gel volume)

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一般描述

DFF100-500Ml′ 的更新产品编号为 GE17-0709-01

应用

DEAE - 琼脂糖凝胶用于亲和层析、蛋白质层析和离子交换层析。 DEAE - 琼脂糖凝胶已被用于研究人类疾病的发病机制,并开发了一种新的检测方法,用于检测艰难梭菌致病菌株的毒素。
DEAE-琼脂糖凝胶用于:
  • 阴离子交换色谱
  • 筛选聚异戊二烯磷酸磷酸酶活性
  • 纯化同工抑制剂
  • 纯化人类免疫缺陷病毒(HIV)
  • 糖蛋白包膜(gp140 env)

生化/生理作用

二乙氨乙基-琼脂糖凝胶(DEAE-琼脂糖凝胶)是强阴离子交换柱,其中DEAE与琼脂糖共价结合。

法律信息

Sepharose is a trademark of Cytiva

替代产品

象形图

Flame

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

法规信息

危险化学品

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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Effective Purification Procedure of <I>Aspergillus oryzae</I> α−Amylase from Solid State Fermentation Cultures Including Concanavalin-A Sepharose
Terebiznik, M.R., et al.
Journal of Food Biochemistry, 19(5), 341-354 (1995)
Rapid high-level production of functional HIV broadly neutralizing monoclonal antibodies in transient plant expression systems
Rosenberg Y, et al.
Testing, 8(3), e58724-e58724 (2013)
Valérie Molinier-Frenkel et al.
Journal of virology, 76(1), 127-135 (2001-12-12)
The capacity of recombinant adenoviruses (rAd) to induce immunization against their transgene products has been well documented. In the present study, we evaluated the vaccinal adjuvant role of rAd independently of its vector function. BALB/c mice received one subcutaneous injection
Growth cone collapse and neurite retraction from cultured <I>Helisoma</I> neurons in response to antibody Fab fragments against an extracellular matrix protein.
Miller, J.D., et al.
Dev. Brain Res., 79(2), 203-218 (1994)
T M Schmidt et al.
Applied and environmental microbiology, 55(10), 2607-2612 (1989-10-01)
Luminescence of batch cultures of Xenorhabdus luminescens was maximal when cultures approached stationary phase; the onset of in vivo luminescence coincided with a burst of synthesis of bacterial luciferase, the enzyme responsible for luminescence. Expression of luciferase was aldehyde limited

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