Cobalt Chelating Resin (8 Citations)

Catalog
Description
Size
Price(USD)
Qty
Catalog
786-286
786-286
Description
Cobalt Chelating Resin
Cobalt Chelating Resin
Size
10ml Resin
10ml Resin
$127.00
$127.00
Catalog
786-402
786-402
Description
Cobalt Chelating Resin
Cobalt Chelating Resin
Size
100ml Resin
100ml Resin
$895.00
$895.00
Catalog
786-403
786-403
Description
Cobalt Chelating Resin
Cobalt Chelating Resin
Size
500ml Resin
500ml Resin
$3,061.00
$3,061.00
Catalog
786-454
786-454
Description
Cobalt Chelating Resin, 0.2ml Spin Column
Cobalt Chelating Resin, 0.2ml Spin Column
Size
25 columns
25 columns
$227.00
$227.00
Catalog
786-455
786-455
Description
Cobalt Chelating Resin, 1ml Spin Column
Cobalt Chelating Resin, 1ml Spin Column
Size
5 columns
5 columns
$146.00
$146.00
Catalog
786-456
786-456
Description
Cobalt Chelating Resin, 3ml Spin Column
Cobalt Chelating Resin, 3ml Spin Column
Size
5 columns
5 columns
$211.00
$211.00
Catalog
786-600
786-600
Description
Cobalt Chelating Resin
Cobalt Chelating Resin
Size
2 x 500ml Resin
2 x 500ml Resin
$5,623.00
$5,623.00
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 | |
786-402 | |
786-403 | |
786-454 | |
786-455 | |
786-456 | |
786-600 |
Technical Literature | |
Plant Proteomics Handbook | |
Protein Purification Handbook |
- Jia, Chen et al (2023) Odorant-binding proteins and chemosensory proteins in Spodoptera frugiperda: from genome-wide identification and developmental stage-related expression analysis to the perception of host plant odors, sex pheromones, and insecticides. INT J MOL SCI. https://doi.org/10.3390/ijms24065595
- Mount, J. et al (2022) Structural basis for mechanotransduction in a potassium-dependent mechanosensitive ion channel. NAT COMMUN. https://doi.org/10.1038/s41467-022-34737-0
- Pedersen, Jannie et al (2022) An adaptable platform for in-house hepatitis C serology. J VIROL METHODS. https://doi.org/10.1016/j.jviromet.2022.114586
- Zhang, Wei et al (2022) An odorant binding protein is involved in counteracting detection-avoidance and Toll-pathway innate immunity. J ADV RES. https://doi.org/10.1016/j.jare.2022.08.013
- Zimmerman, Ofer et al (2022) mRNA vaccine boosting enhances antibody responses against SARS-CoV-2 Omicron variant in individuals with antibody deficiency syndromes. CELL REP MED. https://doi.org/10.1016/j.xcrm.2022.100653
- Blais, N et al, (2020) FUSION PROTEINS AND COMBINATION VACCINES COMPRISING. Doi: freepatentsonline.com/y2020/0331972.html
- Sharma, A. et al (2017) Crystallization and Preliminary X-ray Diffraction Analysis of CsaA from P. torridus: A Chaperone Rarely Found in Archaea . Current Chemical Biology 11:63
- Ma, H. and O'Kennedy, R. (2013) Recombinant antibody fragment production, Methods. doi.org/10.1016/j.ymeth.2016.11.008
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Immobilized Metal Ion Affinity Chromatography (IMAC), developed by Porath (1), is based on the interaction of certain protein residues (histidines, cy..
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