menu
Your Cart

Cobalt Chelating Resin (3 Citations)







Immobilized Metal Ion Affinity Chromatography (IMAC), developed by Porath (1), is based on the interaction of certain protein residues (histidines, cysteines, and to some extent tryptophans) with cations of transition metals. 
 
The Cobalt Chelating Resin is specifically designed for the purification of proteins that associate with Cobalt ions, including 6x histidine tagged proteins. Although 6 X His tagged proteins bind with a slightly lower efficiency compared to Nickel Chelating Resin there is a significant reduction in non-specific binding. Cobalt resins have a higher selectivity for poly-His sequences, however have a low loading capacity, therefore Cobalt Chelating Resin should be used for valuable recombinant proteins in limited quantities.
 
Immobilized metal affinity chromatography (IMAC) resin utilizing cobalt (Co2+) for the purification of 6x histidine tagged proteins.
 
This resin binds to six histidine residues (6x His), a common tag used in protein purification. The resin consists of iminodiacetate coupled to 6% cross-linked agarose beads. The iminodiacetate binds divalent cobalt ion with a capacity of 20-40μmoles Co2+/ml resin.  The protein binding capacity is >50mg protein per ml resin.  We have demonstrated binding of >100mg of a 50kDa 6XHis tagged proteins to a ml of resin.
 
The spin columns are supplied with a resin bed volume of 0.2, 1 and 3ml with total column volumes of 1, 8 and 22ml respectively. Columns can be used as a spin format of gravity flow columns.
 
Immobilized Nickel, Copper and Zinc Chelating Resins are also available.  Cobalt has the highest selectivity followed by Zinc, Nickel then Copper, but has the lowest loading capacity.  Copper has the highest loading capacity, followed by Nickel then Zinc.
 
Specific binding/wash and elution buffers are available.
 
Our new HOOK™ 6X His Protein Purification kits are now available and include everything required for purification of 6X His tagged proteins from yeast or bacteria, including lysis buffers, lytic enzymes, resin, columns and binding, wash and elution buffers. Each kit is available with nickel or cobalt chelating resins. Kits available are:
HOOK™ 6X His Protein Purification (Bacteria): Isolation from bacteria; optimized to yield up to 10mg/250ml culture of soluble 6X His tagged protein.
HOOK™ 6X His Protein Spin Purification (Bacteria): Isolation from bacteria;optimized to yield ~1mg/50ml culture of soluble 6X His tagged protein
HOOK™ 6X His Protein Purification (Yeast): Isolation from yeast; optimized to yield up to 10mg of soluble 6X His tagged protein.
HOOK™ 6X His Protein Spin Purification (Yeast): Isolation from yeast; optimized to yield up to 1mg of soluble 6X His tagged protein.
 

 


Features

  • For the purification of Cobalt Binding proteins, including 6x His proteins
  • High capacity: >50mg/ml
  • Ligand density: 20-40μmoles Co2+ /ml resin
  • Bead Structure: 6% cross-linked agarose

 


Applications

  • Affinity purification of cobalt binding proteins
  • Affinity purification of proteins with a 6x His tag.

 

 

Protocol
786-286
786-402
786-403
786-454
786-455
786-456
786-600
Material Safety Data Sheet
786-286
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
786-402
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
786-403
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
786-454
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
786-455
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
786-456
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
786-600
English_US
Danish
Dutch
English_UK
French
German
Spanish
Norwegian
Portuguese
Finnish
Swedish
Polish
Technical Literature
Plant Proteomics Handbook
Protein Purification Handbook

Write a review

Note: HTML is not translated!
Bad Good
Captcha

CONNECT WITH US