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 Location: Home > Products > Protein Purification > Chromatography Columns and Media > Affinity, Metal Chelate > IMAC Sepharose High Performance Media/HiTrap IMAC HP Columns
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Last updated:09/02/2010

IMAC Sepharose High Performance Media/HiTrap IMAC HP Columns

  • For optimizing purification of histidine-tagged* proteins when Ni2+ is not the best choice of metal ion.
  • Conveniently charge with your metal of choice.
  • Small bead size for high performance purification.
  • High binding capacity.
  • Prepacked HiTrap columns for convenient purification.
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IMAC Sepharose High Performance Media/HiTrap IMAC HP Columns

Technical Information


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* For licensing information, see Legal Info.

TECHNICAL SPECIFICATIONS
Matrix Highly cross-linked agarose, 6% 
Average particle size 34 μm 
Binding capacity At least 40 mg histidine-tagged protein/ml medium when charged with Ni2+ 
Compatibility Stable in all commonly used buffers 
Chemical stability* For one week at 40°C: 0.01 M HCl, 0.1 M NaOH
For 12 h: 1M NaOH, 70% acetic acid
30 min tested 30% 2-propanol
1 h tested 2% SDS 
pH stability* 3-12 (long term), 2-14 (short term) 
HiTrap™ prepacked columns
Column volume 1 ml and 5 ml 
Column dimensions 0.7 × 2.5 cm (1 ml), 1.6 × 2.5 cm (5 ml) 
Recommended flow rate 1 ml/min (1 ml), 5 ml/min (5 ml) 
Max. pressure 3 bar (0.3 MPa, 42 psi) 
Storage 20% ethanol 
Storage temperature 4°C to 30°C 
* Medium uncharged with metal ions.
H2O at room temperature.
Protein- and metal-ion dependent.

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Purification of GFP-(His)6 from E. coli lysate using HiTrap IMAC HP column charged with different metal ions.

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SDS-PAGE of GFP-(His)6 fractions purified with different metal ions according to the chromatogram above.



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