产品名称
亚氨基二乙酸琼脂糖, aqueous ethanol suspension
SMILES string
[X]N(CC(=O)O)CC(=O)O
form
aqueous ethanol suspension
matrix
Sepharose 6B Fast Flow
matrix activation
epoxy
matrix attachment
amino
matrix spacer
7 atoms
capacity
22-30 μmol/mL binding capacity (Zn2+)
storage temp.
2-8°C
Quality Level
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Application
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).
General description
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.
Physical form
Suspension in 20% ethanol
Legal Information
Sepharose is a trademark of Cytiva
hcodes
signalword
Warning
Hazard Classifications
Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
96.8 °F
flash_point_c
36 °C
法规信息
危险化学品
此项目有
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)
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
Histidine-rich glycoprotein from the hemolymph of the marine mussel Mytilus edulis L. binds Class A, Class B, and borderline metals
Devoid SJ, et al.
Environmental Toxicology and Chemistry / Setac, 26(5), 872-877 (2007)
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