
Products
SHBC provides colored microspheres, fluorescent microspheres, magnetic beads, silica microspheres, chromatography packing microspheres and biological reagents for diagnostic assay development, nucleic acid extraction, protein purification and separation applications.
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MNi10UM-10
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SHBC
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5%
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10µm
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10ml,20ml,50ml ,500ml,1000ml
10um Nickel Magnetic Beads MNi10UM-10
SHBC MNi10UM-10 Nickel Magnetic Beads are 10 μm magnetic microspheres with a nickel-affinity surface and 5% solid content.
They are designed for magnetic capture, separation and purification of His-tagged proteins in research and process-development workflows.
Product Overview
MNi10UM-10 combines a 10 μm particle size, nickel affinity and convenient magnetic separation.
The beads provide a solid phase for capturing polyhistidine-tagged recombinant proteins from clarified lysates, protein solutions and other compatible samples.
The concentrated 5% suspension supports flexible dilution, repeated purification experiments and bulk applications.
Technical Specifications
Parameter | Specification |
|---|---|
Product Name | Nickel Magnetic Beads |
Product Code | MNi10UM-10 |
Brand | SHBC |
Manufacturer | Shanghai SanYu Biotechnology Co., Ltd. |
Nominal Particle Size | 10 μm |
Solid Content | 5% |
Surface Type | Nickel-Affinity Surface |
Chelating Ligand | Refer to Product Specification |
Product Form | Magnetic Bead Suspension |
Target | His-Tagged Proteins |
Separation Method | Magnetic Separation |
Supply Scale | Sample, Pilot and Bulk Supply |
Binding capacity, nickel loading, magnetic response and buffer composition are specification-dependent. Refer to the applicable TDS and COA.
Key Advantages
Nominal particle size of 10 μm
Concentrated 5% solids
Nickel-affinity surface
Convenient magnetic collection
No centrifugation required for bead separation
Suitable for His-tagged protein capture
Easy washing and buffer exchange
Suitable for manual workflow development
Suitable for multiwell plate evaluation
Flexible packaging and bulk supply
How Do Nickel Magnetic Beads Work?
Nickel-affinity purification is based on immobilized metal affinity chromatography, commonly called IMAC.
Histidine residues in a His tag interact with immobilized nickel ions on the bead surface. A magnet then collects the beads while unbound sample components are removed.
After washing, the captured protein can be eluted using a validated buffer system.
Applications of 10um Nickel Magnetic Beads
His-Tagged Protein Purification
MNi10UM-10 is suitable for capturing and purifying recombinant proteins containing accessible polyhistidine tags.
Recombinant Protein Screening
The beads can support rapid screening of His-tagged protein expression from multiple samples.
Magnetic Protein Separation
A compatible magnetic separator enables convenient bead collection, washing and liquid removal.
Protein Pull-Down Assays
His-tagged bait proteins may be immobilized on the beads for protein-interaction and pull-down research.
His-Tagged Protein Immobilization
MNi10UM-10 can support immobilization of His-tagged proteins for downstream binding and analytical studies.
High-Throughput Workflow Development
The beads may be evaluated in tubes, multiwell plates and automated magnetic-separation systems.
Native and Denaturing Purification
Nickel-affinity purification can be developed under native or selected denaturing conditions, depending on the bead formulation and target protein.
Benefits of 10um Particle Size
The 10 μm particle format provides convenient handling during magnetic collection, washing and resuspension.
Typical formats include:
Microcentrifuge tubes
Magnetic separation racks
Multiwell plates
Automated liquid-handling systems
Small-scale protein purification
Process optimization experiments
Benefits of 5% Solid Content
MNi10UM-10 is supplied at 5% solids as a concentrated magnetic bead suspension.
Users can adjust the bead amount according to sample volume, target concentration and purification requirements.
The concentrated format supports repeated experiments, pilot projects and larger-volume production needs.
Typical His-Tag Purification Workflow
1. Resuspend the Beads
Mix the suspension thoroughly before sampling to obtain a uniform bead concentration.
2. Wash and Equilibrate
Collect the beads with a magnet, remove the storage solution and equilibrate them with a compatible binding buffer.
3. Add the Sample
Add clarified lysate or protein solution and mix gently to promote interaction between the His tag and nickel surface.
4. Perform Magnetic Separation
Collect the beads with a compatible magnet and remove the unbound fraction.
5. Wash the Beads
Wash the beads to reduce nonspecific proteins and other sample components.
6. Elute the Target Protein
Elute the captured protein using an optimized imidazole, pH-based or other compatible elution method.
Conditions should be optimized for each target protein and sample matrix.
Buffer Compatibility and Optimization
Nickel-affinity performance may be affected by:
Buffer pH
Salt concentration
Imidazole concentration
Detergents
Reducing agents
Denaturants
Chelating agents
Sample viscosity
Incubation time
His-tag accessibility
Strong chelating agents may remove nickel ions and reduce binding performance. Compatibility should be confirmed before use.
Factors Affecting Protein Recovery
Protein recovery and purity depend on:
Position of the His tag
Accessibility of the His tag
Target protein concentration
Bead-to-sample ratio
Binding time
Mixing efficiency
Wash stringency
Elution conditions
Competing proteins
Sample composition
Small-scale optimization is recommended before pilot or batch processing.
Quality and Batch Documentation
Available documentation may include:
Product code
Batch number
Nominal particle size
Solid content
Product appearance
Surface type
Certificate of Analysis
Safety Data Sheet
Technical Data Sheet
Binding capacity and magnetic response should only be stated according to the applicable SHBC specification.
Why Choose SHBC?
Shanghai SanYu Biotechnology Co., Ltd. supplies magnetic beads and functional microspheres for biomolecule separation, protein purification and assay development.
SHBC supply advantages include:
Multiple magnetic bead sizes
Nickel and other functional surfaces
Laboratory sample supply
Pilot-scale manufacturing
Bulk production capability
Customized solid content
Flexible packaging volumes
OEM and private-label services
Technical product-selection support
Customized Nickel Magnetic Beads
Customization options may include:
Particle diameter
Particle-size distribution
Solid content
Nickel-affinity surface
Chelating ligand
Dispersion medium
Buffer system
Packaging volume
OEM labeling
Bulk production
Storage and Handling
Store MNi10UM-10 according to the product label, TDS, COA and SDS.
Thoroughly resuspend the beads before sampling. Avoid allowing the beads to dry during washing or purification.
Use clean laboratory tools and a compatible magnetic separator. Do not freeze unless freezing compatibility is confirmed in the product specification.
Frequently Asked Questions
What is MNi10UM-10?
MNi10UM-10 is a 10 μm nickel-affinity magnetic bead suspension with a solid content of 5%.
What are nickel magnetic beads used for?
They are mainly used for magnetic capture, separation, purification and immobilization of His-tagged proteins.
What is a His-tagged protein?
A His-tagged protein contains a short sequence of histidine residues that enables affinity binding to immobilized nickel ions.
What is IMAC?
IMAC means immobilized metal affinity chromatography. It uses immobilized metal ions to capture proteins containing accessible histidine residues.
Can MNi10UM-10 purify 6×His-tagged proteins?
The beads are designed for polyhistidine-tagged protein capture. Performance depends on tag accessibility, sample composition and purification conditions.
Is centrifugation required?
A compatible magnet can be used to collect the beads, so centrifugation is generally not required for bead separation.
Can imidazole be used?
Imidazole is commonly evaluated during binding, washing and elution. The appropriate concentration depends on the target protein and sample.
Can EDTA be used?
Strong chelating agents such as EDTA may remove nickel ions from the surface and reduce binding performance.
Can the beads be used under denaturing conditions?
Selected denaturing conditions may be evaluated after compatibility with the bead formulation has been confirmed.
What is the binding capacity?
Binding capacity depends on the surface chemistry, target protein and purification conditions. Refer to the applicable SHBC technical specification.
Can MNi10UM-10 be used in automated systems?
The beads may be evaluated in multiwell plate and automated magnetic-separation workflows.
Are bulk quantities available?
Yes. SHBC supports laboratory samples, pilot projects, customized packaging and bulk production.
Request MNi10UM-10 Samples and Quotations
Contact Shanghai SanYu Biotechnology Co., Ltd. for MNi10UM-10 samples, technical specifications, customized packaging and bulk quotations.
SHBC supplies nickel magnetic beads for His-tagged protein purification, affinity capture, protein immobilization and research applications.
For Research Use Only.


