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G-Sep™ Co IDA Agarose Fast Flow

G-Sep™ Co IDA Agarose Fast Flow
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G-Sep™ Co IDA Agarose Fast Flow
G-Sep™ Co IDA Agarose Fast Flow
Catalog Description Size Price (USD) Qty
786-977G-Sep™ Co IDA Agarose Fast Flow5ml$93.00
786-978G-Sep™ Co IDA Agarose Fast Flow25ml$380.00
786-979G-Sep™ Co IDA Agarose Fast Flow100ml$1,264.00
786-980G-Sep™ Co IDA Agarose Fast Flow500ml$5,427.00
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  • Description
    Immobilized Metal Ion Affinity Chromatography (IMAC), developed by Porath (1975), is based on the interaction of certain protein residues (histidines, cysteines, and to some extent tryptophans) with cations of transition metals.  G-Sep™ Co IDA Agarose Fast Flow is specifically designed for the purification of recombinant proteins fused to the 6x histidine (6XHis) tag.  Both nickel and cobalt IDA are offered as nickel has a higher binding affinity, but lower specificity compared to cobalt.  This means that although cobalt IDA has a slightly lower efficiency compared to nickel IDA resin there is a significant reduction in non-specific binding.
     
    The resin is  specifically designed for the purification of recombinant proteins fused to the 6x histidine (6XHis) tag expressed in bacteria, insects, and mammalian cells.  The resin is high affinity and selectivity for recombinant fusion proteins that are tagged with six tandem histidine residues.  
     
    G-Sep™ Co IDA Agarose Fast Flow (FF) resin is cobalt ions immobilized onto highly cross-linked 6% agarose beads using iminodiacetic acid groups (IDA). The G-Sep™ IDA Agarose Fast Flow (FF) resins have high chemical stability, allowing well proven cleaning-in-place (CIP) and sanitization protocols. G-Sep™ Ni IDA Agarose Fast Flow (FF) resin using nickel is also available
     
     


    Features

    • Matrix: Cross-linked agarose beads, 6%
    • Bead form: Spherical, diameter 50-160μm
    • Spacer: Epichlorohydrin
    • Chelating Agent: Iminodiacetic acid
    • Active group: Co2+
    • Co2+ density: 20-40μmol /ml
    • Binding Capacity: 5-10mg His-tagged protein/ml medium
    • pH stability Working Range: 3-12
    • pH stability Cleaning-in-Place (CIP): 2-14
    • Maximum Flow Velocity: 450cm/h
    • Exclusion limit(globular proteins): 4 x 106
    • Physical Stability: Negligible volume variation due to changes in pH or ionic strength
    • Chemical Stability: Stable to all commonly used aqueous buffers: 6M urea, 8M guanidine hydrochloride,
    • Autoclavable: 121°C, pH 7, for 30 min
    • Storage Conditions: 2 to 8°C, 20% Ethanol

     


    Applications

    • Immobilized meatl affinity chromatography (IMAC)
    • Purification of 6X His tagged proteins
    • Purification of cobalt binding proteins

     

     

  • Reviews
Immobilized Metal Ion Affinity Chromatography (IMAC), developed by Porath (1975), is based on the interaction of certain protein residues (histidines, cysteines, and to some extent tryptophans) with cations of transition metals.  G-Sep™ Co IDA Agarose Fast Flow is specifically designed for the purification of recombinant proteins fused to the 6x histidine (6XHis) tag.  Both nickel and cobalt IDA are offered as nickel has a higher binding affinity, but lower specificity compared to cobalt.  This means that although cobalt IDA has a slightly lower efficiency compared to nickel IDA resin there is a significant reduction in non-specific binding.
 
The resin is  specifically designed for the purification of recombinant proteins fused to the 6x histidine (6XHis) tag expressed in bacteria, insects, and mammalian cells.  The resin is high affinity and selectivity for recombinant fusion proteins that are tagged with six tandem histidine residues.  
 
G-Sep™ Co IDA Agarose Fast Flow (FF) resin is cobalt ions immobilized onto highly cross-linked 6% agarose beads using iminodiacetic acid groups (IDA). The G-Sep™ IDA Agarose Fast Flow (FF) resins have high chemical stability, allowing well proven cleaning-in-place (CIP) and sanitization protocols. G-Sep™ Ni IDA Agarose Fast Flow (FF) resin using nickel is also available
 
 


Features

  • Matrix: Cross-linked agarose beads, 6%
  • Bead form: Spherical, diameter 50-160μm
  • Spacer: Epichlorohydrin
  • Chelating Agent: Iminodiacetic acid
  • Active group: Co2+
  • Co2+ density: 20-40μmol /ml
  • Binding Capacity: 5-10mg His-tagged protein/ml medium
  • pH stability Working Range: 3-12
  • pH stability Cleaning-in-Place (CIP): 2-14
  • Maximum Flow Velocity: 450cm/h
  • Exclusion limit(globular proteins): 4 x 106
  • Physical Stability: Negligible volume variation due to changes in pH or ionic strength
  • Chemical Stability: Stable to all commonly used aqueous buffers: 6M urea, 8M guanidine hydrochloride,
  • Autoclavable: 121°C, pH 7, for 30 min
  • Storage Conditions: 2 to 8°C, 20% Ethanol

 


Applications

  • Immobilized meatl affinity chromatography (IMAC)
  • Purification of 6X His tagged proteins
  • Purification of cobalt binding proteins

 

 

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