PROTEIN G SEPHAROSE 4 FF
产品名称: PROTEIN G SEPHAROSE 4 FF
英文名称: PROTEIN G SEPHAROSE 4 FF
产品编号: 17061801
产品价格: 0
产品产地: 美国
品牌商标: GE
更新时间: null
使用范围: null
上海基星生物科技有限公司
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17-0618-01 | PROTEIN G SEPHAROSE 4 FF, 5 ML |
17-0618-02 | PROTEIN G SEPHAROSE 4 FF, 25 M |
17-0618-05 | PROTEIN G SEPHAROSE 4FF 200 ML |
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17-0700-01 | 2,5 ADP-SEPHAROSE 4B 5 G |
17-0756-01 | GLUTATHIONE SEPHAROSE 4B 10 ML |
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17-0885-01 | GAMMABIND G SEPHAROSE, 5 ML |
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17-0886-01 | GAMMABIND PLUS SEPHAROSE, 5 ML |
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Protein G Sepharose™ 4 Fast Flow
- High capacity, high flow rate fractionation of monoclonal antibodies at both laboratory and process scales, without binding albumin.
- Rapid processing of large volumes, recoveries of 70-90%.
- Binds to all IgG subclasses from human, mouse, and rat; binds total IgG from guinea pig, rabbit, goat, cow, sheep, and horse
Protein G Sepharose™ 4 Fast Flow
Technical Information
TECHNICAL SPECIFICATIONS | |
Ligand | Recombinant protein G lacking albumin-binding region |
Ligand coupling method | Cyanogen bromide activation |
No.of IgG binding | 2 sites per ligand |
MW of ligand | ~17 000 |
pI of ligand | 4.1 |
Degree of substitution | ~2 mg Protein G/ml drained medium |
Number of IgG binding sites per ligand | 2 |
Matrix | Highly cross-linked agarose, 4% |
Binding capacity | > 20 mg human IgG/ml medium |
Average particle size | 90 μm |
Ligand density | » 2 mg Protein G/ml medium |
Chemical stability | Stable to all commonly used aqueous buffers - 1 M acetic acid, 1% SDS, and 6 M guanidine HCl (tested at 37°C for 7 days), as well as, 0.1 M glycine NaOH pH 11, 1 M HC1, and 8 M urea (stable for at least 2 h at room temperature) |
pH stability | 3-9 (working), 2*-10 (short term) |
Physical stability | Negligible volume variation due to changes in pH or ionic strength |
Sanitization | Do not autoclave.Wash the column with 70% ethanol. |
Antimicrobial agent | 20% ethanol |
Storage | 20% ethanol |
Storage temperature | 4°C to 8°C |
* pH below 3 is sometimes required to elute strongly bound IgG species. However, protein ligands may hydrolyze at very low pH.
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Purification of human monoclonal antibody using Protein G Sepharose™ 4 Fast Flow (1).
Reference
- Jungbauer, A. et al. Comparison of protein A, protein G and copolymerised hydroxyapatite for the purification of human monoclonal antibodies. J. Chromatogr. 476, 257 (1989).