Chromatography Media
- (1)
- (1)
- (4)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (4)
- (3)
- (2)
- (2)
- (3)
- (2)
- (3)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (3)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (3)
- (2)
- (7)
- (2)
- (1)
- (2)
- (22)
- (8)
- (3)
- (5)
- (6)
- (4)
- (1)
- (1)
Filtered Search Results
Cytiva TALON™ Superflow Medium
Offers different selectivity compared to nickel-charged media. Cytiva TALON™ Superflow Medium used for purification of histidine-tagged recombinant proteins by IMAC.
| Particle Size | 60 to 160 μm |
|---|---|
| Ligand Type | Talon Superflow Cobalt-IMAC |
| Matrix | 6% Cross-Linked Agarose |
| Storage Buffer | 20% Ethanol |
| pH Range | 3 to 12 |
| Product Type | Talon Superflow Media |
| Binding Capacity | Up to 20 mg Histidine-tagged Protein |
| Storage Requirements | 4°C to 8°C |
| For Use With (Application) | For PurifiCatIon of Histidine-Tagged Recombinant Pby Immobilized Metal Affinity Chromatography |
Cytiva Sephaorose™ Fast Flow Anion Exchange Media: DEAE
Used for preparative protein separations in both research and industrial applications. Cytiva Life Sciences™ Sephaorose™ Fast Flow Anion Exchange Media: DEAE ensures low levels of non-specific binding.
Cytiva SP Sepharose™ High Performance Media
Use for high intermediate and polishing steps in downstream processing. Cytiva Life Sciences™ SP Sepharose™ High Performance Media is composed of crosslinked agarose beads.
Cytiva Capto™ MMC ImpRes Multimodal BioProcess™ Chromatography Medium
For high-resolution polishing of monoclonal antibodies (MAbs) and other biomolecules
| Particle Size | 40 μm |
|---|---|
| Ligand Type | Multimodal Weak CatIon Exchanger |
| Matrix | High-flow Agarose |
| Stability | 1 M Acetic Acid, 1 M NaOH, 2 M NaCl, 5% 1-Propanol, 30% Isopropanol, 70% Ethanol |
| Storage Buffer | 20% Ethanol, 0.2 M Sodium Acetate |
| pH Range | 3 to 12 |
| Product Type | Capto MMC ImpRes Media |
| Binding Capacity | 60 to 90 mg Mab/mL |
| Anion Exchange Capacity | 25 to 39 μM/mL |
| Storage Requirements | 4°C to 30°C |
| For Use With (Application) | For High Resolution Polishing of Monoclonal Antibodies (MAbs) and Other Biomolecules |
| Max. Pressure | 300 kPa |
Cytiva HiTrap™ Capto™ PlasmidSelect
For the purification of supercoiled DNA to high quality for gene therapy and DNA vaccine applications
| Matrix | Capto™ PlasmidSelect |
|---|---|
| Length (Metric) | 2.5 cm |
| Product Type | Chromatography Resin |
| For Use With (Application) | Purification of Supercoiled DNA From Research Scale to cGMP Production |
| Max. Pressure | 5 bar (0.5 MPa) |
Cytiva His SpinTrap™ TALON™
Single-use spin column for high purity purification of histidine-tagged proteins
Cytiva MabSelect Sure™ LX Chromatography Media
Protein A affinity medium with high dynamic binding capacity which improves performance and cuts costs
| Stability | Stable in aqueous Buffers commonly used in Protein A Chromatography |
|---|---|
| Storage Buffer | 20% Ethanol |
| pH Range | 3 to 12 |
| Height (English) Bed | 7.87 in. |
| Storage Requirements | 2°C to 8°C |
| For Use With (Application) | For PurifiCatIon of Monoclonal Antibodies for Clinical AppliCatIons |
| Max. Pressure | <2 bar |
| Includes | Certificate of Analysis |
| Particle Size | 85 μm |
| Ligand Type | Alkali-stabilized Protein A-derived (E. coli) |
| Flow Rate | 500 cm/Hoμr |
| Matrix | Highly Cross-Linked Agarose |
| Product Type | MabSelect SuRe LX Media |
| Binding Capacity | 60 mg Human IgG/mL mediμm |
| Height (Metric) Bed | 20 cm |
Cytiva Phenyl Sepharose™ 6 Fast Flow Chromatography Media
Used for capture and intermediate purification requiring low to medium hydrophobicity
| Ligand Type | Phenyl |
|---|---|
| Matrix | 6% Cross-Linked Agarose |
| pH Range | 3 to 13 |
| For Use With (Application) | For Capture and Intermediate PurifiCatIon Requiring Low to Medium Hydrophobicity |
Cytiva Q Sepharose™ High Performance Chromatography Media
Designed for high intermediate and polishing steps in downstream processing
Cytiva Sephaorose™ Fast Flow Anion Exchange Media: ANX
Used for preparative protein separations in both research and industrial applications
| pH Range | 3 to 13 pH |
|---|---|
| Product Type | ANX Sepharose 4 Fast Flow |
| For Use With (Application) | For Protein Separations in Research/Industrial Applications |
Cytiva MabSelect Xtra™ Chromatography Media
Provides high purity capture and high dynamic binding capacity
| Particle Size | 75 μm |
|---|---|
| Ligand Type | Recombinant Protein A (E. coli) |
| Flow Rate | <300 cm/Hoμr |
| Matrix | Highly Cross-Linked Agarose |
| Storage Buffer | 20% Ethanol |
| pH Range | 2 to 12 |
| Product Type | MabSelect Xtra Media |
| Binding Capacity | 40 mg Human lgG/mL (at 2.4 min. residence time) |
| Height (English) Bed | 7.87 in. |
| Storage Requirements | 2°C to 8°C |
| For Use With (Application) | For Develop to Meet The Demands of Increasing Levels of Expression in Monoclonal Antibody Feedstocks |
| Height (Metric) Bed | 20 cm |
| Max. Pressure | <200 kPa |
Cytiva SOURCE™ 15S Chromatography Media
Chemically stable cation exchanger for high resolution polishing purification of proteins, peptides and oligonucleotides
| Stability | Stable in common Ion Exchange Buffers |
|---|---|
| Storage Buffer | 20% Ethanol, 0.2 M Sodium Acetate |
| pH Range | 1 to 14 |
| Height (English) Bed | 3.93 in. |
| Storage Requirements | 4°C to 30°C |
| For Use With (Application) | For High Resolution Polishing PurifiCatIon of Proteins, Peptides and Oligonucleotides |
| Max. Pressure | 100 kPa |
| Particle Size | 15 μm |
| Ligand Type | Sulphonate Group |
| Flow Rate | 400 cm/Hoμr |
| Matrix | Polystyrene/Divinylbenzene |
| Product Type | Source 15 S Media |
| Ion Exchange Type | Strong CatIon Exchanger |
| Height (Metric) Bed | 10 cm |
Cytiva Q Sepharose™ XL
Hydrophilic base matrix ensures low levels of non-specific binding leading to low levels of host cell-derived impurities in elution pool