I4510
Iminodiacetic acid Sepharose™
aqueous ethanol suspension
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Synonym(s):
Iminodiacetic acid Agarose, IDA Resin
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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
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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
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3
WGK
WGK 1
Flash Point(F)
96.8 °F
Flash Point(C)
36 °C
Regulatory Information
危险化学品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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)
Isolation of isoelectric species of phosphorylated rhodopsin.
J H McDowell et al.
Methods in enzymology, 315, 70-76 (2000-03-29)
Pierluigi Pilla et al.
Biosensors & bioelectronics, 31(1), 486-491 (2011-12-06)
We present a fast and effective method for anchoring bioreceptors to optical waveguides exhibiting a poorly reactive polymer interface and that have to be minimally perturbed with respect to their design. The study originated from the need to biofunctionalize a
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