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Cytiva Capto™ Core 700
Capto Core 700 is designed for intermediate purification and polishing of viruses and other large biomolecules.
$379.00 - $1015.00
Specifications
Buffer | 1M NaOH, 6M Guanidine Hydrochloride, 30% Isopropanol and 70% Ethanol |
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Product Type | Capto Core 700 chromato graphy media |
Flow Rate | <500cm/hr. |
Ligand Type | Octylamine |
pH Range | 2 to 14 |
Catalog Number | Mfr. No. | Quantity | Price | Quantity & Availability | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity & Availability | |||||
45-002-596
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Cytiva
17548102 |
100mL |
Each for $1,015.00
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45-002-595
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Cytiva
17548101 |
25mL |
Each for $379.00
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Description
The novel core bead technology and multimodal, octylamine ligand give Capto Core 700 dual functionality, size exclusion, and binding chromatography in one chromatography medium (resin).
- For intermediate purification and polishing of viruses and other large biomolecules (Mr > 700 000) in flowthrough mode.
- Novel core bead technology allows efficient capture of contaminants while target molecules are collected in the flowthrough.
- Significantly improved productivity and higher flow rates compared with gel filtration methods.
- Straightforward optimization due to flowthrough chromatography and robust performance.
- Convenient small-scale purification, process development, and scale-up using prepacked HiTrap and HiScreen columns.
- Capto Core 700 is composed of a ligand-activated core and inactive shell.
- The inactive shell excludes large molecules (cut off ∼ Mr 700000 [700 kDa]) from entering the core through the pores of the shell.
- These larger molecules are collected in the column flowthrough while smaller impurities bind to the internalized ligands.
- The core of each bead is functionalized with ligands that are both hydrophobic and positively charged, resulting in a highly efficient multimodal binding of various contaminants small enough to enter the core.
- The multimodal ligands ensure strong binding with most impurities over a wide range of pH and salt concentrations.
- Bound impurities are removed from the beads by cleaning-in-place (CIP) procedures using NaOH and in most cases, a solvent.
Specifications
1M NaOH, 6M Guanidine Hydrochloride, 30% Isopropanol and 70% Ethanol | |
<500cm/hr. | |
2 to 14 | |
Highly Cross-linked Agarose | |
Intermediate purification and polishing of viruses and other large biomolecules |
Capto Core 700 chromato graphy media | |
Octylamine | |
90μm | |
4° to 30°C | |
Multimodal Resin |
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