I4510
Iminodiacetic acid Sepharose™
aqueous ethanol suspension
Synonym(s):
Iminodiacetic acid Agarose, IDA Resin
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
form
aqueous ethanol suspension
Quality Segment
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
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
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
96.8 °F
flash_point_c
36 °C
Regulatory Information
危险化学品
This item has
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.
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)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I4510-25ML | 04061833856888 |
| I4510-10ML | 04061837766060 |