Cat# | Product Name | Size | Price | Qty | Inquiry |
---|---|---|---|---|---|
Bu-413C | Butyl Sepharose High Performance | Inquiry |
Product Information | |
Cat#No# | Bu-413C |
Product Overview | Butyl Sepharose High Performance is an aliphatic hydrophobic interaction chromatography (HIC) medium, designed for intermediate and polishing step purification steps when high resolution has priority. |
Description | Butyl Sepharose High Performance is a member of the Cytiva range of HIC resins for intermediate purification and polishing of proteins. Butyl Sepharose High Performance is based on highly crosslinked, 34-µm agarose beads modified with aliphatic butyl groups via uncharged, chemically stable ether linkages. It is a truly hydrophobic resin displaying a minimum of ionic interactions. Butyl Sepharose High Performance resins is particularly well suited for intermediate purification and polishing steps providing high resolution due to the small particle size. |
Characteristic | High-resolution, high-capacity separations with high recovery. Reliable and reproducible. High chemical stability for effective CIP and sanitization. Available in laboratory and BioProcess scale quantities. Easy to scale up. |
Maximum operating pressure | Base matrix: 100-200 cm/h, 300 kPa, BioPilot 60/600 column, bed height 30 cm. |
Matrix | cross-linked agarose |
Particle Size | 24 µm-44 µm |
Average particle size | ~34 µm |
Ligand | Butyl |
Ligand density | Approx. 50 µmol butyl/ml gel |
Dynamic binding capacity | ~ 38 mg β-lactoglobulin/mL resin |
Recommended flow rate | ≤ 100 cm/h |
Recommended column height | 30 cm |
Chemical stability | Stable in commonly used aqueous buffers - 1 M sodium hydroxide, 1 M acetic acid, 8 M urea, 6 M guanidine hydrochloride, 30% acetonitrile, 70% ethanol, 3 M ammoniumsulfate, 1 mM HCl, 30% isopropanol, 2% SDS |
pH working range | 3–13 |
CIP stability | 2–14 |
Cleaning-in-place | Removal of precipitated proteins: Wash the column with 4 bed volumes of 0.01 M NaOH at 40 cm/h, followed by 2 to 3 bed volumes of water. Removal of tightly bound hydrophobic proteins, lipoproteins and lipids: Wash the column with 4 to 10 bed volumes of up to 70% ethanol or 30% isopropanol followed by 3 to 4 bed volumes of water. Alternatively, wash the column with detergent in a basic or acidic solution, for example, 0.5% nonionic detergent in 1 M acetic acid. Wash at a flow velocity of 40 cm/h. Remove residual detergent with 5 bed volumes of 70% ethanol followed by 3 to 4 bed volumes of water. |
Sanitization | Wash the column with 0.01 M NaOH at a flow velocity of approximately 40 cm/h, contact time 30 to 60 min. |
Pack size | 25 mL |
BioProcess resin | Yes |
Maximum flow velocity | 4.0 mL/min (1 mL), 20 mL/min (5 mL) |
Dimensions | 0.7 × 2.5 cm (1 mL), 1.6 × 2.5 cm (5 mL) |
Column volume | 1 mL and 5 mL |
Column hardware pressure limit | 5 bar (0.5 MPa, 73 psi) |
Download Datasheet |
For Research or Industrial Raw Materials, Not For Personal Medical Use!
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