IMAC HyperCel™ Sorbent for Immobilized Metal Affinity Chromatography (IMAC)
Ideal for Tagged Biomolecule
Purification Using IMAC
- Metal-chelate affinity chromatography exploits the affinity of proteins or other molecules for metal ions.
- Can be used in combination with standard chromatography columns, disposable gravity flow columns, disposable Nanosep® centrifugal filters and AcroPrep™ multi-well filter plates.
- Uses tridentate IDA (iminodiacetic acid) as a chelating ligand agent. This ligand is immobilized on the HyperCel base sorbent, a stable, robust and well-known sorbent used for both research and industrial-scale protein separations.
- Prior to use, metal ions can be immobilized on the IMAC HyperCel resin.
- Purification of His-tagged proteins
- Purification of phosphoproteins and phosphopeptides
- Purification of antibodies
- Fractionation of complex protein mixtures
Particle Size
- 80-100 µm
Typical Working Pressure
- < 1 bar (100 kPa, 14 psi)
Capacity for Metal Ions
- 40-70 µmol Cu2 per mL of sorbent
Ionic Capacity
- 90-140 µeq/mL
Regeneration
- 0.5-1.0 M NaOH
Pressure Resistance
- < 3 bar (300 kPa, 44 psi)
Working pH
- 3 - 12
Storage Temperature
- 2-8 °C (36-46 °F)
High Purity Protein in a Single Step Using Native Conditions

M: Protein molecular weight marker
L: Sample loaded on the column
FT: Unbound/flow through
W: Wash fraction
E: Eluate
Marked area on gel demonstrates single-step affinity purification of His-tagged protein purified under native conditions.
High Purity Protein in a Single Step Using Denaturing Conditions

M: Protein molecular weight marker
L: Sample loaded on the column
FT: Unbound/flow through
W: Wash fraction
E: Eluate
Marked area on gel demonstrates single-step affinity purification of His-tagged protein purified under denaturing conditions.
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