Hi-Bind™ Protein G-Agarose

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SKU:
26-6513
Availability:
Usually Shipped in 5 Working Days
Packaging:
EA
Storage Temperature:
+4°C
Shipping Conditions:
gel pack
Shelf Life:
12 months
£244.24 - £4,457.38
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Description

Hi-BindTM Protein G-Agarose beads are specially prepared for high IgG binding by covalently coupling recombinant Protein G to 6% cross-linked Agarose beads, the most popular resin for protein affinity purification methods. BioVision’s Protein G (Cat. # 6510) is a genetically engineered protein containing three IgG-binding regions of native Protein G. The cell wall binding region, albumin binding region and other non-specific regions have been eliminated from the recombinant Protein G to ensure the maximum specific IgG binding. The coupling technique is optimized to give a higher binding capacity for IgG & minimum leaching of recombinant Protein G than the other regular Protein-G Agarose on the market. The IgG binding capacity of Hi-BindTM Protein G-Agarose is ≥ 30 mg of human or rabbit IgG per ml of wet beads. The Hi-BindTM Protein G-Agarose beads are stable in chemical & physical properties with high flow rate, hydrophilicity & high gel strength.

Sort Name: Protein G-Agarose

Taglines: Reusable Protein G conjugated hi bind agarose beads with ≥30 mg/ml binding capacity & 2.89 ml/min flow rate for antibody purification from multiple sources

Product Highlights: • CONTENTS: Supplied as 50% slurry in 20 % Ethanol/H2O. • FEATURES: - HIGH BINDING CAPACITY: Binding of IgG ≥ 30 mg human or rabbit IgG/ml Protein G-Agarose. - MINIMAL LEACHING OF THE LIGAND - FLOW RATE TESTED*: 2.89 ml/min *Test condition: Calculations based on the time required to pass 18 ml of water through 2 ml settled beads (column diameter 1.5 cm). - MAXIMUM FLOW RATE* = 1800 cm/hr; minimum leaching of recombinant Protein G. NOTE * = the highest flow that beads withstand for 1 min, without collapsing and the pressure reaching 1 MPa. - USAGE: Reusable for up to 10 times without significant loss of binding capacity. • APPLICATIONS - Purification of monoclonal and polyclonal antibodies from culture media, serum, ascites fluid or hybridoma supernatants. - Isolation of antibody/antigen complexes in immunoprecipitation experiments, since only the Fc region is involved in antibody binding and the Fab region is available for binding antigen.

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