产品名称
DEAE - 琼脂糖凝胶™, Fast Flow
form
suspension
technique(s)
affinity chromatography: suitable
matrix
6% cross-linked agarose
bead size
45-165 μm (wet)
pore size
~4,000,000 Da exclusion limit
pH
2—12
capacity
110-160 μeq/mL binding capacity(gel volume)
Quality Level
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Application
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)
Biochem/physiol Actions
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。
General description
DFF100-500Ml′ 的更新产品编号为 GE17-0709-01
Legal Information
Sepharose is a trademark of Cytiva
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
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
法规信息
危险化学品
此项目有
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)
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)
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)
Ahmet Mavi et al.
Journal of enzyme inhibition and medicinal chemistry, 21(2), 235-239 (2006-06-23)
The inhibition and activation effects of some drugs on the activities of superoxide dismutase enzymes (SOD) in human erythrocyte and leukocyte cells was investigated. Firstly, CuZnSOD enzyme was purified 837-fold and 12% efficiency from human erythrocytes by ethanol-chloroform treatment to
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