Affinity chromatography media, MabSelect Xtra™
MabSelect Xtra has the same recombinant Protein A ligand as MabSelect but is based on a high-flow agarose base matrix with increased porosity and a slightly decreased particle size compared to MabSelect.
- Higher dynamic binding capacity than currently available Protein A chromatography media
- High purity capture due to high ligand selectivity and matrix hydrophilicity
- Epoxy activation coupling method
- Slightly lower pressure/flow properties compared to MabSelect SuRe and MabSelect
- Improved process economics through reduced raw materials costs and/or reduced number of cycles
- Prepacked, ready-to-use columns for convenient process development
- Easily connected in series to achieve 20 cm bed height
- Small bed volume gives fast results and minimal sample/buffer consumption
MabSelect Xtra is available in a range of different bulk pack sizes and convenient pre-packed formats for easy scale-up and process development. As member of the BioProcess media range, MabSelect Xtra meets industrial demands with security of supply and comprehensive technical and regulatory support. The medium provides a lower overall production cost due to the possibility of processing concentrated feedstocks in fewer batches.
This results in higher capacity—MabSelect Xtra has about 30% higher dynamic binding capacity for IgG than currently available Protein A chromatography media. In addition, MabSelect Xtra has a higher capacitiy for many Fc-fusion proteins.
MabSelect Xtra has the same recombinant Protein A ligand as MabSelect but is based on a high-flow agarose base matrix with increased porosity and a slightly decreased particle size compared to MabSelect.
- Higher dynamic binding capacity than currently available Protein A chromatography media
- High purity capture due to high ligand selectivity and matrix hydrophilicity
- Epoxy activation coupling method
- Slightly lower pressure/flow properties compared to MabSelect SuRe and MabSelect
- Improved process economics through reduced raw materials costs and/or reduced number of cycles
- Prepacked, ready-to-use columns for convenient process development
- Easily connected in series to achieve 20 cm bed height
- Small bed volume gives fast results and minimal sample/buffer consumption
MabSelect Xtra is available in a range of different bulk pack sizes and convenient pre-packed formats for easy scale-up and process development. As member of the BioProcess media range, MabSelect Xtra meets industrial demands with security of supply and comprehensive technical and regulatory support. The medium provides a lower overall production cost due to the possibility of processing concentrated feedstocks in fewer batches.
This results in higher capacity—MabSelect Xtra has about 30% higher dynamic binding capacity for IgG than currently available Protein A chromatography media. In addition, MabSelect Xtra has a higher capacitiy for many Fc-fusion proteins.
- Catalog No:
- 17-5269-07
- 17-5269-02
- Ligand:
- Recombinant protein A (E.coli)
- Recombinant protein A (E.coli)
- Matrix:
- Highly cross-linked agarose
- Highly cross-linked agarose
- Flowhastighed:
- <300 cm/h
- <300 cm/h
- pH-område:
- 3 - 10
- 3 - 10
- Bindingskapacitet:
- 40 mg human lgG/ml
- 40 mg human lgG/ml
- Opbevaringstemperatur:
- 2 - 8 °C
- 2 - 8 °C
Product Family Options
- BeskrivelseModelPartikelstørrelsePakn
Specifications
Cat. No.17-5269-07LigandRecombinant protein A (E.coli)MatrixHighly cross-linked agaroseFlowhastighed<300 cm/hpH-område3 - 10Bindingskapacitet40 mg human lgG/mlOpbevaringstemperatur2 - 8 °C- MabSelect Xtra™Liquid75 µm200 ml1 * 200 mL51.860,00 kr
Specifications
Cat. No.17-5269-02LigandRecombinant protein A (E.coli)MatrixHighly cross-linked agaroseFlowhastighed<300 cm/hpH-område3 - 10Bindingskapacitet40 mg human lgG/mlOpbevaringstemperatur2 - 8 °C
Recommendations will be personalized based on your shopping preferences only if you have given your consent by enabling "Enhance my Shopping Experience" on the "Personal Info page".
Otherwise, you will receive generic recommendations.



