I4510
Iminodiacetic acid Sepharose™
aqueous ethanol suspension
Synonym(s):
Iminodiacetic acid Agarose, IDA Resin
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
form
aqueous ethanol suspension
Quality Level
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
SMILES string
[X]N(CC(=O)O)CC(=O)O
Looking for similar products? Visit Product Comparison Guide
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.
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).
Physical form
Suspension in 20% ethanol
Legal Information
Sepharose is a trademark of Cytiva
related product
Product No.
Description
Pricing
replaced by
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
96.8 °F
Flash Point(C)
36 °C
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
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)
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)
Isolation of isoelectric species of phosphorylated rhodopsin.
J H McDowell et al.
Methods in enzymology, 315, 70-76 (2000-03-29)
B Sutter et al.
Protein expression and purification, 19(1), 53-56 (2000-06-02)
The superoxide dismutases (EC 1.15.1.1) are a family of enzymes that catalyze the dismutation of superoxide radical anion to dioxygen and hydrogen peroxide. The active site contains a critical metal ion such as manganese, iron, or copper. The copper-containing protein
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service