rProtein A Sepharose™ Fast Flow Affinity Purification Media, Cytiva

Supplier: Cytiva
Sepharose™
17-1279-02 17-1279-01 17127903 17-1279-02 17-1279-02 17127901 17-1279-03
CA97067-986EA 1730.56 CAD
97067-896 97067-992 95017-086 CA97067-986 CA97067-896 97067-986 CA95017-086
rProtein A Sepharose™ Fast Flow Affinity Purification Media, Cytiva
Protein Purification Protein Purification Resins
rProtein A Sepharose™ 4 Fast Flow is a well established antibody affinity medium is designed for the purification of monoclonal and polyclonal antibodies based on Sepharose™ Fast Flow platform. The recombinant protein A is produced in E.coli and engineered for an oriented coupling to giving a matrix with enhanced binding capacity. The epoxy-based coupling ensures low ligand leakage. The specificity of the recombinant protein A for the Fc region of IgG is similar to native protein A and provides excellent purification in one step. The high capacity, low ligand leakage and a well established base matrix makes rProtein A Sepharose™ Fast Flow ideal for purification of monoclonal antibodies at both laboratory and process scale.

  • For antibody affinity chromatography
  • High dynamic binding capacity due to oriented, single-point attachment of protein A
  • Well-established Protein A medium used in many approved MAb processes
  • Epoxy activation coupling method
  • No mammalian components involved during the manufacturing process
  • Stable in all aqueous buffers commonly used in protein A chromatography - 10 mM HCI (pH 2), 10 mM NaOH (pH 11), 0.1 M sodium citrate/HCl (pH 3), 6 M GuHCl, 20% ethanol

rProtein A Sepharose 4 Fast Flow 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, rProtein A Sepharose 4 Fast Flow meets industrial demands with security of supply and comprehensive technical and regulatory support.

It is composed of recombinant protein A coupled to the cross-linked 4% agarose base matrix. The recombinant protein A is produced in E. coli and has been specially engineered to favour an oriented coupling giving a matrix with enhanced binding capacity. The epoxy based coupling ensures low ligand leakage. The specificity of the recombinant protein A for the Fc region of IgG is similar to native protein A, giving a high purification factor in a single step. The high capacity, low ligand leakage and a well established base matrix makes rProtein A Sepharose 4 Fast Flow suitable for purification of monoclonal antibodies at both laboratory and process scale.
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