His-tag Protein Purification Beads (IDA-Co)
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His-tag Protein Purification Beads (IDA-Co)

Cat.No: SM-HMM-0059 Datasheet

Specification Quantities

5 mL:
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2×50 mL:
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4×250 mL:
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Product Details Product Overview Related Products
Product Name His-tag Protein Purification Beads (IDA-Co)
Catalog No. SM-HMM-0059
Description Cobalt Ion Chelated Magnetic Beads for His-tag Protein Purification
Features Direct purification of target proteins from crude samples, greatly reducing the purification time;
Easily control the concentration and volume of target protein;
High purity of target protein can be obtained in one step;
High stability of parallel operation, which is convenient for high throughput and large-scale protein purification;
High yield of target protein can be obtained;
Reusable and easy to regenerate.
Storage 2-8°C
Shelf Life 2 years
Average Particle Size 30-150 µm
Concentration 10% (v/v)
Product Introduction These magnetic beads are charged with cobalt ions (Co2+) via an immodiacetic acid (IDA) linker, creating a high-affinity matrix for the purification of recombinant proteins containing a polyhistidine (His) tag (typically 6xHis). The Co2+ ions offer superior specificity over traditional nickel-charged beads, reducing non-specific binding of host cell proteins, especially those containing endogenous metal-binding motifs. The magnetic format enables rapid, batch-mode purification under native or denaturing conditions directly from crude lysates without the need for columns or centrifugation.
Product Application • One-step purification of His-tagged proteins from bacterial, mammalian, or insect cell lysates.
• Small-scale screening of expression conditions and solubility.
• Pull-down assays to capture His-tagged proteins and their interactors.
• Automated, high-throughput protein purification workflows.
Product Advantages • Enhanced Specificity (Cobalt): Cobalt chemistry provides higher selectivity for the His-tag compared to nickel, resulting in purer protein preparations with fewer contaminating proteins.
• High Binding Capacity: The beads offer a high density of charged metal ions, enabling efficient capture even from dilute lysates or for high-yield expressions.
• Magnetic Workflow Efficiency: Enables rapid washing and elution steps using a simple magnet, streamlining the process and reducing hands-on time significantly.
• Gentle Elution Options: Proteins can be eluted under native conditions using low concentrations of imidazole or competitively with EDTA, helping to preserve protein structure and activity.

For research use only, not for clinical use.

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