
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.
-
CPS/DVB200UM
-
SHBC
-
10%
-
200µm
-
10ml,20ml,50ml,100ml,1000ml
200 μm Carboxyl Crosslinked PS/DVB Microspheres CPS/DVB200UM
SHBC CPS/DVB200UM Carboxyl Crosslinked PS/DVB Microspheres are large 200 μm functional polymer beads featuring a crosslinked polystyrene/divinylbenzene matrix and reactive surface carboxyl groups.
Supplied at 10% solids, CPS/DVB200UM is designed for antibody coupling, protein immobilization, biomolecule capture, large-bead immunoassay research and custom functional particle development.
The 200 μm particle format provides straightforward handling, rapid settling and convenient recovery for laboratory research and scalable batch processing.
CPS/DVB200UM Technical Specifications
Property | Specification |
|---|---|
Product Name | Carboxyl Crosslinked PS/DVB Microspheres |
Product Code | CPS/DVB200UM |
Particle Size | 200 μm |
Polymer Matrix | Crosslinked PS/DVB |
Surface Group | Carboxyl (-COOH) |
Solid Content | 10% |
Main Function | Covalent Biomolecule Immobilization |
Brand | SHBC |
Manufacturer | Shanghai SanYu Biotechnology Co., Ltd. |
Crosslinked PS/DVB Polymer Matrix
CPS/DVB200UM uses divinylbenzene to form a crosslinked polystyrene network.
Crosslinking increases the rigidity and structural stability of large polystyrene particles. Commercial suppliers offer crosslinked PS microspheres in the approximately 175–210 μm and 200–600 μm size ranges for large-particle applications.
Key benefits include:
Rigid polymer structure
Stable spherical particle format
Good mechanical handling
Convenient repeated washing
Easy particle recovery
Suitable for surface functionalization
Suitable for batch processing
Carboxyl Surface for Covalent Biomolecule Coupling
The particle surface contains carboxyl (-COOH) groups that can be activated for covalent coupling with amine-containing biomolecules.
Typical coupling route:
Carboxyl Surface → EDC/NHS Activation → Amine-Containing Biomolecule → Amide Bond
Carboxyl-functional polystyrene and PS/DVB microspheres are established substrates for carbodiimide-mediated attachment of proteins and other amine-containing molecules.
Key Advantages of CPS/DVB200UM
Large 200 μm particle size
High 10% solid content
Crosslinked PS/DVB matrix
Reactive carboxyl surface
Suitable for EDC/NHS coupling
Stable covalent ligand immobilization
Rapid particle settling
Easy washing and recovery
Suitable for batch biomolecule coupling
Suitable for research and bulk production
Why Choose 200 μm Carboxyl Microspheres?
The 200 μm particle format is especially suitable when easy physical recovery and large-particle handling are more important than maximizing surface area per unit mass.
Potential advantages include:
Rapid sedimentation
Easy visual observation
Convenient centrifugation
Easy filtration or sieving where appropriate
Straightforward washing
Reduced loss during liquid exchange
Convenient batch coupling
Suitable for large-bead assay formats
Easy scale-up of particle handling
Large crosslinked PS beads in the 200 μm range are already commercially used for protein-related and bead-bed applications, demonstrating the usefulness of this particle size class.
Immunoassay Applications
Antibody-Coupled Large Microspheres
Capture antibodies can be covalently immobilized on CPS/DVB200UM for research applications such as:
Heterogeneous bead-based immunoassays
Antigen capture studies
Biomarker-binding research
Serological assay development
Antibody-antigen interaction studies
Custom diagnostic reagent development
Because 200 μm particles are much larger than conventional latex immunoassay particles, they are better suited to large-bead heterogeneous assay formats than homogeneous turbidimetric assays.
Antigen-Coupled Microspheres
Diagnostic or research antigens can also be immobilized for:
Antibody detection
Serology research
Autoantibody research
Infectious-disease assay development
Antibody-binding studies
Assay optimization
Protein and Biomolecule Immobilization
CPS/DVB200UM can also be evaluated for:
Protein immobilization
Enzyme immobilization
Peptide coupling
Affinity ligand preparation
Biomolecule capture
Biosensor development
Surface chemistry research
Amino-modified oligonucleotide coupling
Custom functional bead preparation
Suitable Coupling Molecules
The carboxyl-functional surface can be evaluated with:
Monoclonal antibodies
Polyclonal antibodies
Recombinant proteins
Diagnostic antigens
Peptides
Enzymes
Amino-modified DNA
Amino-modified RNA
Other amine-containing ligands
Final coupling efficiency depends on ligand properties and optimized reaction conditions.
General EDC/NHS Coupling Workflow
1. Resuspend CPS/DVB200UM
Mix the microspheres thoroughly before sampling.
Because 200 μm particles settle rapidly, resuspend immediately before transferring the suspension.
2. Wash the Microspheres
Wash with a suitable activation buffer.
Large particles are generally easy to recover during washing.
3. Activate Surface Carboxyl Groups
Add EDC, with or without NHS, to activate the surface -COOH groups.
4. Add the Biomolecule
Add purified antibody, antigen, protein or another amine-containing ligand.
5. Perform Covalent Coupling
Allow activated carboxyl groups to react with primary amines on the biomolecule.
6. Block Residual Reactive Sites
Use a suitable quenching or blocking reagent.
7. Wash and Resuspend
Remove unbound ligand and coupling reagents, then resuspend the functionalized particles in the selected assay or storage buffer.
EDAC/EDC-mediated coupling is a commonly used strategy for covalent immobilization of amine-containing molecules on carboxyl polymer microspheres.
Factors Affecting Coupling Efficiency
Important optimization factors include:
Microsphere concentration
Protein concentration
EDC concentration
NHS concentration
Activation pH
Coupling-buffer composition
Reaction temperature
Reaction time
Mixing method
Blocking conditions
Small-scale coupling studies are recommended before transferring the process to bulk production.
Handling Tips for 200 μm Microspheres
Large microspheres behave differently from nano- and small-micron particles.
Recommended handling practices include:
Mix before every sampling step.
Maintain gentle agitation during coupling.
Prevent prolonged settling.
Use wide-bore pipette tips when necessary.
Avoid unnecessarily narrow tubing.
Minimize transfer steps.
Confirm particle recovery after washing.
Avoid aggressive mechanical agitation.
Validate mixing during process scale-up.
CPS/DVB200UM vs. Smaller Carboxyl Microspheres
Feature | 200 μm Microspheres | Smaller Microspheres |
|---|---|---|
Particle Handling | Very easy | More careful handling required |
Sedimentation | Very fast | Slower |
Washing | Easy recovery | Higher particle-loss risk |
Visual Observation | Easy | Difficult |
Surface Area per Mass | Lower | Higher |
Suspension Stability | Requires frequent mixing | Better |
Typical Use | Large-bead batch processes | High-surface-area assays |
Smaller particles generally provide greater surface area per unit mass, while 200 μm particles prioritize handling and recovery.
200 μm Carboxyl PS/DVB vs. Standard Large PS Beads
Feature | CPS/DVB200UM | Standard Large PS Beads |
|---|---|---|
Particle Size | 200 μm | Large particle range |
Polymer Matrix | Crosslinked PS/DVB | Crosslinked or standard PS |
Surface Group | Carboxyl (-COOH) | Often non-functional |
Protein Attachment | Covalent coupling | Mainly adsorption if unmodified |
EDC/NHS Coupling | Yes | Not without COOH modification |
Typical Use | Biomolecule immobilization | General particle applications |
Commercial 200 μm-scale crosslinked PS beads are widely available, but many standard large-particle products are supplied without reactive surface functionalization.
Covalent Coupling vs. Passive Protein Adsorption
Feature | Carboxyl Covalent Coupling | Passive Adsorption |
|---|---|---|
Binding Mechanism | Chemical bond | Physical interaction |
Typical Method | EDC/NHS | Direct incubation |
Ligand Retention | Strong | Condition-dependent |
Washing Stability | Higher | Variable |
Process Complexity | Moderate | Simple |
Typical Application | Stable functional beads | Rapid protein coating |
Quality Control for Bulk Production
For research and immunoassay reagent development, recommended evaluation parameters include:
Particle-size consistency
Particle morphology
Solid-content consistency
Surface carboxyl functionality
Suspension behavior
Coupling efficiency
Ligand loading
Recovery after washing
Nonspecific binding
Assay signal
Storage stability
Batch-to-batch consistency
Why Choose SHBC CPS/DVB200UM?
200 μm carboxyl crosslinked PS/DVB microspheres
High 10% solid-content suspension
Reactive COOH surface
Suitable for EDC/NHS chemistry
Designed for antibody and protein immobilization
Easy large-particle recovery
Suitable for batch coupling
Suitable for immunoassay research
Sample evaluation available
Bulk manufacturing capability
Custom quantity and packaging support
Storage and Handling
Recommended practices include:
Keep the container tightly sealed.
Mix thoroughly before sampling.
Resuspend settled particles before use.
Avoid unnecessary freezing.
Prevent microbial contamination.
Use suitable pipette tips for large particles.
Avoid conditions causing irreversible aggregation.
Validate storage conditions after biomolecule coupling.
Frequently Asked Questions
What is CPS/DVB200UM?
CPS/DVB200UM is a 200 μm carboxyl-functional crosslinked polystyrene/divinylbenzene microsphere product supplied at 10% solids.
What does PS/DVB mean?
PS/DVB means polystyrene crosslinked with divinylbenzene.
Why use DVB-crosslinked polystyrene?
Crosslinking creates a more rigid and structurally stable polymer particle, which is especially useful for large microsphere formats.
What is the purpose of the carboxyl surface?
Carboxyl groups provide reactive sites for covalent attachment of antibodies, proteins and other amine-containing molecules.
Can antibodies be coupled to CPS/DVB200UM?
Yes. Antibodies can be immobilized using optimized EDC or EDC/NHS chemistry.
Can CPS/DVB200UM be used for immunoassays?
Yes. It is primarily suited to large-bead heterogeneous immunoassay research, antigen capture and biomolecule-binding studies.
Is CPS/DVB200UM suitable for latex turbidimetric immunoassays?
200 μm particles are much larger than typical latex particles used in homogeneous turbidimetric assays. Smaller microspheres are generally more appropriate for PETIA and latex agglutination formats.
Can CPS/DVB200UM be used in flow cytometry?
200 μm particles are outside the typical particle range of most conventional flow cytometers. Instrument compatibility should be confirmed before use.
What is the solid content?
CPS/DVB200UM is supplied at 10% solids.
Can amino-modified DNA or RNA be coupled?
Yes. Amino-modified oligonucleotides may be evaluated for carbodiimide-mediated coupling to the carboxyl surface.
Why choose 200 μm instead of smaller microspheres?
200 μm particles provide very easy recovery, washing and physical handling. Smaller particles provide substantially greater surface area per unit mass.
Do 200 μm microspheres settle quickly?
Yes. Regular resuspension or gentle mixing is recommended during coupling and assay procedures.
Can SHBC supply bulk quantities?
Yes. SHBC supports sample evaluation and bulk production for biotechnology companies, immunoassay developers and research organizations.
Request CPS/DVB200UM Samples
Contact Shanghai SanYu Biotechnology Co., Ltd. for CPS/DVB200UM samples, technical documentation and bulk quotations.
Please provide:
Target antibody or protein
Intended application
Coupling chemistry
Required quantity
Assay format
Development stage
Estimated annual demand
CPS/DVB200UM is supplied for research and process development. Final diagnostic applications should be validated by the customer.


