Ni Sepharose™ excel Immobilised Metal Ion Affinity Chromatography (IMAC) Media, Cytiva

Supplier: Cytiva
Sepharose™
17371202 17-3712-02 17371203 17-3712-01 17371203 17371201 17371202 17371203 17371202 17-3712-03
CA89234-478EA 12865.08 CAD
CA89234-478 89234-476 89234-478 CA89234-476 CA89233-410 CA11022-612 89233-410 CA89233-408 89233-408 89428-612
Ni Sepharose™ excel Immobilised Metal Ion Affinity Chromatography (IMAC) Media, Cytiva
Protein Purification Protein Purification Resins
Ni Sepharose™ excel is an IMAC medium pre-charged with nickel ions very strongly bound to a chelating ligand. Samples that usually cause stripping of metal ions can, therefore, be loaded to the medium. Ni Sepharose™ excel is designed primarily for capture and purification of histidine-tagged proteins secreted into cell culture supernatants from eukaryotic cells such as insect cells or CHO cells.

  • Load eukaryotic cell culture samples containing secreted histidine-tagged proteins directly with retained binding capacity
  • Increase target protein yield and decrease degradation through reduced and simplified sample handling
  • Choose between several formats for screening and preparative purification of histidine-tagged proteins

Ni Sepharose excel enables direct loading of samples without having to perform extensive and time-consuming pretreatment procedures. The flow properties of the medium make it excellent for purifications in a wide range of scales and allow loading of large sample volumes, enabling purification of low concentrations of target proteins at large volumes. Dynamic binding capacity was tested with 0.5 mg/ml (histidine)6-tagged pure protein (Mr 43 000) in EX-CELL™ 420 Insect serum-free medium (capacity at 10% breakthrough) or (histidine)6-tagged protein (Mr 28 000). Column volume was 1 ml and flow rate 1 ml/min. Binding capacity is sample-dependent.

Samples that usually cause stripping of metal ions can therefore be loaded to the medium. The nickel ions have been shown to remain bound to the chelating ligand even after incubation for 24 hours in 10 mM EDTA. Ni Sepharose excel is designed primarily for capture and purification of histidine-tagged proteins secreted into cell culture supernatants from eukaryotic cells such as insect cells or CHO cells.
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