| Cat# | Product Name | Size / Price | Qty | Inquiry |
|---|---|---|---|---|
| Be-344C | Benzamidine Sepharose 4 Fast Flow (High Sub) | Inquiry |
| Cat#No# | Be-344C |
| Product Overview | Benzamidine Sepharose 4 Fast Flow (High Sub) is an excellent tool for removal of proteolytic activity from a protein. Benzamidine Sepharose 4 Fast Flow (high sub) is based on highly cross-linked 4% agarose enabling high flow rates without losing binding capacity. p-aminobenzamidine (pABA) immobilized on Sepharose 4 Fast Flow matrix gives high productivity, and allows easy scale-up. Effective removal of thrombin and factor Xa after tag cleavage of recombinant proteins. For convenient, one-step removal and/or purification of trypsin, trypsin-like serine proteases, and zymogens including urokinase and prekallikrein. |
| Description | Benzamidine Sepharose 4 Fast Flow (high sub) is an excellent tool for removal and/or purification of trypsin and trypsin-like serine proteases, as well as, zymogens including urokinase and prekallikrein. Removal of serine proteases is easily done directly from serum, monoclonal cell supernatants and bacterial lysates. |
| Characteristic | Benzamidine Sepharose 4 Fast Flow (high sub) is based on highly crosslinked 4% agarose, which enables rapid processing of large sample volumes. The ligand, paminobenzamidine, is covalently coupled via an amide bond to a long spacer arm attached to Sepharose 4 Fast Flow via a stable ether linkage. Coupling is optimized to give high binding capacity. Total binding capacity is ≥ 35 mg trypsin per mL medium. |
| Maximum operating pressure | base matrix min 150 cm/h, 100 kPa, XK 50/60 column, bed height 25 cm. |
| Ligand Coupling Method | Amide |
| Packing Column | Benzamidine Sepharose 4 Fast Flow (high sub) is supplied in 0.05 M acetate buffer pH 4 containing 20% ethanol as a bacteriostat. Decant the solution and replace it with binding buffer before use. In general, we recommend a bed height of 5–15 cm to allow high flow rates to be used. |
| Matrix | Highly cross-linked 4% agarose |
| Average particle size | ~90 µm |
| Ligand | p-aminobenzamidine [pABA] |
| Ligand density | > 12 µmol p-aminobenzamidine/ml medium |
| Recommended flow rate | 30 cm/h - 300 cm/h |
| Recommended column height | 25 cm |
| Chemical stability | Commonly used aqueous buffers |
| pH working range | 2–8 |
| CIP stability | 1–9 |
| Storage | 2 to 8°C, 0.05 M Sodium Acetate, pH 4.0 in 20% Ethanol |
| Shipping | Supplied in 0.05 M acetate buffer, pH 4 containing 20% ethanol. |
| Cleaning-in-place | The general recommendation is to use a solution of guanidine hydrochloride to remove precipitated or denatured substances. For hydrophobically bound substances, a solution of non-ionic detergent or ethanol is recommended. |
| Sanitization | For sanitization of Benzamidine Sepharose 4 Fast Flow, we recommend storage in a solution containing 0.1 M acetic acid/20% ethanol. |
| Pack size | 100 mL |
| Maximum flow velocity | 300 cm/h |
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