表单
aqueous ethanol suspension
基质
Sepharose 6B Fast Flow
基质活化
epoxy
基质附着
amino
基质隔离区
7 atoms
容量
22-30 μmol/mL binding capacity (Zn2+)
储存温度
2-8°C
SMILES字符串
[X]N(CC(=O)O)CC(=O)O
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一般描述
I4510-50ML′s updated product number is GE17-0575-01
Iminodiacetic acid Sepharose™ is a chelating resin used for the purification of proteins.
Iminodiacetic acid Sepharose™ is a chelating resin used for the purification of proteins.
应用
Iminodiacetic acid Sepharose™ has been slurry-packed into a tared polypropylene column for immobilized metal-ion affinity chromatography (IMAC) and for the preparation of the chelating sepharose column. It is an important component of metal affinity chromatography which immobilizes transition metal ions.
Iminodiacetic acid Sepharose™ is used is affinity chromatography, protein chromatography and chelating resins. Iminodiacetic acid Sepharose™ has been used to report a new procedure for the purification of two human monoclonal anti-HIV (human immunodeficiency virus) antibodies (mAbs 2G12 and 4E10).
外形
Suspension in 20% ethanol
法律信息
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)
96.8 °F
闪点(°C)
36 °C
法规信息
危险化学品
此项目有
Isolation of isoelectric species of phosphorylated rhodopsin.
J H McDowell et al.
Methods in enzymology, 315, 70-76 (2000-03-29)
D Platis et al.
Journal of chromatography. A, 1211(1-2), 80-89 (2008-10-24)
Affinity chromatography on immobilized Protein A is the current method of choice for the purification of monoclonal antibodies (mAbs). Despite its widespread use it presents certain drawbacks, such as ligand instability, leaching, toxicity and high cost. In the present work
Formation of anhydrotetracycline during a high-temperature treatment of animal-derived feed contaminated with tetracycline.
Kuhne, M., et al.
Food Chemistry, 75(4), 423-429 (2001)
Identification and quantification of histidine-rich glycoprotein (HRG) in the blood plasma of six marine bivalves
Abebe AT, et al.
Comparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology, 147(1) (2007)
Purification of native proteins from the cytoplasm and periplasm of Escherichia coli using IMAC and histidine tails: a comparison of proteins and protocols
Lindner P, et al.
Methods, 4(1), 41-56 (1992)
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