Cat# | Product Name | Size | Price | Qty | Inquiry |
---|---|---|---|---|---|
His-111P | HisTrap FF Crude columns | Inquiry |
Product Information | |
Cat#No# | His-111P |
Product Overview | HisTrap FF Crude columns are high binding capacity IMAC columns for his-tagged protein purification when scalability is needed. |
Characteristic | High binding capacity – binds up to 40 mg his-tag protein/mL resin. Excellent flow properties – great performance even at high flow rates. Optimized for unclarified samples – short purification time can minimize potential negative effects, such as degradation and oxidation of proteins. HiTrap column format – compatible with syringe, pump, or chromatography system such as ÄKTA systems or other FPLC systems. |
Applications | Intended for research use only, and shall not be used in any clinical or in vitro procedures for diagnostic purposes. |
Maximum operating pressure | 5 bar [0.5 MPa] (70 psi) |
Metal ion capacity | ~ 15 μmol Ni2+ /ml medium |
Matrix | Highly cross-linked spherical agarose, 6% |
Average particle size | 90 μm |
Dynamic binding capacity | Approx. 40 mg histidine-tagged protein/ml medium. |
Recommended flow rate | 1 ml/min and 5 ml/min for 1 ml and 5 ml column, respectively. |
Recommended column height | 25 mm |
Chemical stability | 0.01 M HCl, 0.1 M NaOH; Tested for one week at 40°C. 1 M NaOH, 70% acetic acid; Tested for 12 h. 2% SDS; Tested for 1 h. 30% 2-propanol; Tested for 30 min. |
Chemical compatibility | Stable in all commonly used buffers, reducing agents, denaturants, and detergents. |
pH working range | 2 to 14 |
CIP stability | 3 to 12 |
Storage | 4 to 30°C, 20% Ethanol |
Cleaning-in-place | Ionically bound proteins: Wash with several column volumes of 1.5 M NaCl, then wash with approx. 10 column volumes of distilled water. Precipitated proteins, hydrophobically bound proteins, and lipoproteins: Wash the column with 1 M NaOH, contact time usually 1 to 2 h (12 h or more for endotoxin removal). Then wash with approx. 10 column volumes of binding buffer, followed by 5 to 10 column volumes of distilled water. Hydrophobically bound proteins, lipoproteins, and lipids: Wash with 5 to 10 column volumes of 30% isopropanol for about 15 to 20 min. Then wash with approx. 10 column volumes of distilled water. Alternatively, wash with 2 column volumes of detergent in a basic or acidic solution. Use, for example, 0.1 to 0.5% nonionic detergent in 0.1 M acetic acid, contact time 1 to 2 h. After treatment, always remove residual detergent by washing with at least 5 column volumes of 70% ethanol1 . Then wash with approx. 10 column volumes of distilled water. |
Pack size | 5 × 1 mL |
Maximum flow velocity | 4 ml/min and 20 ml/min for 1 ml and 5 ml column, respectively. |
Dimensions | 7 × 25 mm |
Column volume | 1 ml |
Column i.d. | 7 mm |
Column hardware pressure limit | 5 bar (0.5 MPa) |
Download Datasheet |
For Research or Industrial Raw Materials, Not For Personal Medical Use!
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