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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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Q TopIEX HP
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SHBC
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6%
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34µm
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25ml 100ml 300ml 1L 5L 10L 20L
34 μm Q HP High-Resolution Anion Exchange Chromatography Media – Q TopIEX HP
SHBC Q TopIEX HP is a high-resolution strong anion exchange chromatography medium based on crosslinked 6% agarose beads with an average particle size of 34 μm.
The smaller particle size provides higher chromatographic resolution, making Q TopIEX HP especially suitable for intermediate purification and polishing of proteins and other biomolecules.
The matrix is functionalized with Q (quaternary ammonium) strong anion exchange groups for efficient charge-based separation.
Q TopIEX HP Technical Specifications
Property | Specification |
|---|---|
Product Name | High-Resolution Anion Exchange Chromatography Media |
Product Series | TopIEX HP |
Product Type | Q HP |
Functional Group | Quaternary Ammonium (Q) |
Ion Exchange Type | Strong Anion Exchanger |
Matrix | Crosslinked Agarose |
Agarose Content | 6% |
Average Particle Size | 34 μm |
Separation Mode | Anion Exchange Chromatography |
Main Positioning | Intermediate Purification & Polishing |
Brand | SHBC |
Manufacturer | Shanghai SanYu Biotechnology Co., Ltd. |
What Is Q HP Chromatography Media?
Q HP is a high-performance strong anion exchange chromatography medium designed for applications where resolution is more important than maximum process flow.
The positively charged Q ligand interacts with negatively charged proteins and other biomolecules under suitable buffer conditions.
The smaller 34 μm particle size creates a more efficient packed bed and supports higher-resolution separation of closely related biomolecules.
Cytiva uses the same general design principle in Q Sepharose High Performance: crosslinked agarose beads with a mean diameter of 34 μm and quaternary Q groups, specifically positioned for intermediate purification and polishing.
34 μm Beads for High-Resolution Separation
Particle size strongly influences chromatographic efficiency.
Compared with larger Fast Flow particles, the 34 μm format provides:
Higher chromatographic resolution
Improved separation efficiency
Better peak definition
Greater ability to resolve closely related components
Suitable performance for intermediate purification
Suitable performance for polishing chromatography
This makes Q TopIEX HP particularly useful when purity and separation resolution are prioritized over maximum flow rate.
6% Crosslinked Agarose Matrix
Q TopIEX HP uses crosslinked 6% agarose as the chromatography matrix.
Key characteristics include:
Hydrophilic agarose matrix
Crosslinked bead structure
34 μm average particle size
Porous structure for biomolecule access
Suitable packed-bed stability
Low nonspecific hydrophobic interaction
Suitable for high-resolution ion exchange chromatography
Cytiva's Q Sepharose High Performance likewise uses 6% crosslinked agarose with a 34 μm mean particle diameter and emphasizes high-resolution downstream purification.
Q Strong Anion Exchange Principle
Q TopIEX HP contains positively charged quaternary ammonium groups.
Under suitable conditions, negatively charged proteins and other biomolecules bind to the Q ligand.
Typical process:
Equilibration → Sample Loading → Binding → Washing → Selective Elution → Regeneration
Binding and separation depend on:
Protein isoelectric point (pI)
Buffer pH
Conductivity
Ionic strength
Salt concentration
Sample composition
Loading amount
Anion exchange chromatography separates biomolecules according to differences in their net surface charge.
Key Advantages of Q TopIEX HP
34 μm average particle size
High-resolution chromatography
Crosslinked 6% agarose matrix
Strong Q anion exchange chemistry
Quaternary ammonium functional groups
Suitable for protein purification
Suitable for intermediate purification
Suitable for polishing chromatography
Suitable for complex biomolecule mixtures
Suitable for process development
Laboratory and bulk supply available
Protein Purification Applications
Q TopIEX HP can be evaluated for separation and purification of:
Recombinant proteins
Enzymes
Peptides
Acidic proteins
Protein complexes
Antibody-related process streams
Other negatively charged biomolecules
Strong Q anion exchange media are widely used for purification of acidic and neutral proteins under suitable operating conditions. Bio-Rad likewise positions its High Q strong anion exchanger for high-resolution purification of proteins and peptides.
Intermediate Purification
Q TopIEX HP is especially suited to intermediate purification after an initial capture step.
Potential goals include:
Increasing product purity
Removing host-cell proteins
Reducing nucleic acid impurities
Separating charged contaminants
Removing process-related impurities
Preparing the product for final polishing
The 34 μm particle size provides higher resolution than larger Fast Flow media, making it suitable when separation selectivity becomes more important after initial capture.
Polishing Chromatography
Polishing is one of the key applications of Q TopIEX HP.
Potential polishing applications include:
Removal of trace impurities
Host-cell protein reduction
DNA reduction
Aggregate-related impurity separation
Product variant separation
Final purity improvement
High-resolution anion exchange chromatography is widely used in downstream polishing because charge differences can help resolve target products from closely related impurities.
Monoclonal Antibody Process Development
Q TopIEX HP may be evaluated in monoclonal antibody downstream purification.
Depending on antibody properties and process conditions, potential applications include:
Intermediate purification
Flow-through polishing
Host-cell protein reduction
Residual DNA reduction
Aggregate-related impurity reduction
Process impurity removal
Final process mode should be selected according to antibody pI, pH, conductivity and impurity profile.
Recombinant Protein Purification
Potential applications include:
Recombinant protein purification
Protein fractionation
Enzyme purification
Intermediate purification
High-resolution polishing
Product-related impurity separation
The smaller HP bead format is especially useful when closely related protein species require improved chromatographic resolution.
Other Bioprocess Applications
Strong anion exchange chromatography may also be evaluated for:
Viral vector purification
Virus purification
Plasmid DNA purification
Nucleic acid purification
Vaccine-related process development
Biopharmaceutical downstream processing
Modern process-scale AEX media are used across proteins, monoclonal antibodies, viruses, viral vectors and plasmid DNA purification workflows.
General Q TopIEX HP Purification Workflow
1. Pack the Column
Prepare a homogeneous slurry and pack Q TopIEX HP into a suitable chromatography column.
2. Equilibrate
Equilibrate the packed bed with the selected starting buffer.
3. Prepare the Sample
Clarify the sample and adjust pH and conductivity to the required binding conditions.
4. Load the Sample
Apply the sample at an optimized flow rate.
5. Wash the Column
Remove unbound and weakly interacting impurities.
6. Elute the Target
Increase salt concentration or modify buffer conditions to selectively elute bound biomolecules.
7. Regenerate
Remove residual bound material using a validated regeneration procedure.
8. Re-Equilibrate
Return the column to the starting conditions before the next cycle.
Factors Affecting Separation Resolution
Important method-development parameters include:
Buffer pH
Protein pI
Conductivity
Salt concentration
Sample volume
Protein concentration
Resin loading
Flow rate
Residence time
Column bed height
Gradient slope
Sample viscosity
For high-resolution purification, loading, flow rate and gradient conditions should be carefully optimized.
Salt Gradient Elution
A salt gradient is commonly used to separate biomolecules according to differences in ionic interaction strength.
Typical strategies include:
Linear gradient
Step gradient
Multi-step gradient
A shallower gradient may improve separation of closely related components, while a steeper gradient can shorten processing time.
The optimal gradient should be established experimentally.
Q TopIEX HP vs. Q TopIEX FF
Feature | Q TopIEX HP | Q TopIEX FF |
|---|---|---|
Average Particle Size | 34 μm | 90 μm |
Matrix | 6% Crosslinked Agarose | 6% Crosslinked Agarose |
Functional Group | Q | Q |
Exchange Type | Strong Anion | Strong Anion |
Main Priority | High Resolution | High Flow |
Typical Stage | Intermediate / Polishing | Capture / Intermediate |
Flow Capability | Moderate | Higher |
Resolution | Higher | Standard Process Resolution |
Choose Q HP when separation resolution and final purity are the main priorities.
Choose Q FF when process throughput and faster flow are more important.
Q Strong Anion Exchange vs. DEAE Weak Anion Exchange
Feature | Q TopIEX HP | DEAE Media |
|---|---|---|
Exchange Type | Strong Anion Exchange | Weak Anion Exchange |
Functional Group | Quaternary Ammonium | Diethylaminoethyl |
Charge Behavior | Stable strong positive charge | More pH dependent |
Separation Mode | AEX | AEX |
Typical Selection | Robust high-resolution AEX | pH-tunable AEX |
Q media are especially useful when robust strong anion exchange behavior is required.
Why Choose 34 μm Instead of 90 μm?
Smaller particles generally improve column efficiency and chromatographic resolution.
Therefore:
34 μm HP media → Higher resolution and polishing
90 μm FF media → Faster flow and higher process throughput
The preferred product depends on the purification stage and process objective.
High-Resolution Process Development
Q TopIEX HP can be evaluated when process developers need:
Better impurity separation
Improved peak resolution
Higher final purity
Separation of closely related proteins
Intermediate purification
Final polishing
Cytiva similarly positions its 34 μm Q High Performance resin specifically where resolution and capacity have priority during intermediate and polishing steps.
Quality Control for Bulk Production
Important quality parameters may include:
Agarose concentration
Average particle size
Particle-size distribution
Bead morphology
Crosslinking consistency
Q functionalization
Ion exchange performance
Chromatographic resolution
Packed-bed stability
Binding performance
Batch-to-batch consistency
Storage stability
Why Choose SHBC Q TopIEX HP?
34 μm high-resolution particles
Crosslinked 6% agarose matrix
Strong Q anion exchange chemistry
Designed for intermediate purification
Designed for polishing chromatography
Suitable for protein purification
Suitable for biopharmaceutical process development
Laboratory sample evaluation
Pilot-scale supply
Bulk manufacturing capability
Custom packaging support
Frequently Asked Questions
What does Q mean?
Q refers to quaternary ammonium, the strong anion exchange functional group.
What does HP mean?
HP means High Performance and identifies the smaller-particle, higher-resolution chromatography series.
Is Q TopIEX HP a strong anion exchanger?
Yes. It uses Q quaternary ammonium strong anion exchange groups.
What is the matrix?
Q TopIEX HP is based on crosslinked 6% agarose.
What is the average particle size?
The average particle size is 34 μm.
Why does Q HP provide higher resolution?
Its smaller 34 μm particles can provide greater packed-bed efficiency and better chromatographic resolution than larger Fast Flow particles.
What is Q TopIEX HP mainly used for?
It is primarily designed for intermediate purification and polishing of proteins and other biomolecules.
What is the difference between Q HP and Q FF?
Q HP uses smaller 34 μm particles and prioritizes resolution. Q FF uses larger 90 μm particles and prioritizes fast flow and process throughput.
Can Q TopIEX HP be used for monoclonal antibody purification?
Yes. It may be evaluated for suitable intermediate and polishing steps in monoclonal antibody downstream processes.
Can it be used for recombinant proteins?
Yes. Q TopIEX HP can be evaluated for high-resolution purification and polishing of recombinant proteins.
Can Q TopIEX HP remove DNA and host-cell proteins?
Strong anion exchange chromatography can be used to reduce negatively charged process impurities such as DNA and selected host-cell proteins. Performance should be validated for each process.
What is the dynamic binding capacity?
Binding capacity depends on the test molecule, buffer, conductivity, residence time and test method. Use SHBC product-specific QC data rather than specifications from another manufacturer's Q HP resin.
What is the maximum flow rate?
Maximum recommended flow depends on column geometry, bed height and pressure. SHBC product-specific pressure-flow data should be used when defining operating conditions.
Can SHBC supply bulk quantities?
Yes. Shanghai SanYu Biotechnology Co., Ltd. supports laboratory evaluation, pilot-scale requirements and bulk supply of Q TopIEX HP chromatography media.
Request Q TopIEX HP Samples and Bulk Pricing
Contact Shanghai SanYu Biotechnology Co., Ltd. for Q TopIEX HP samples, technical information and bulk quotations.
Please provide:
Target protein or biomolecule
Target protein pI
Feed material
Purification stage
Required resolution
Column dimensions
Required resin volume
Development or production scale
Estimated annual demand
SHBC Q TopIEX HP is designed for research, process development, intermediate purification and high-resolution polishing applications.


