Ni-NTA Superflow 96 BioRobot Kit
- Fully automated purification of up to 10 mg protein per well
- High-purity protein free from cross-contamination
- Purification under native or denaturing conditions
The Ni-NTA Superflow 96 BioRobot Kit provides automated purification of up to 600 µg recombinant protein from 96 samples in parallel (standard protocol, 5 ml culture volume per sample). Cleared bacterial cell lysates flow onto a filter plate preloaded with Ni-NTA Superflow by the BioRobot workstation. This unique 96-well metal-chelate affinity-chromatography module strongly and selectively binds His-tagged proteins. Ready-to-run protocols are provided for purification under native or denaturing conditions.
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Cat No./ID:969261 Ni-NTA Superflow 96 BioRobot Kit (4) $1,502.00 For 4 x 96 6xHis-tagged protein preps: 4 QIAfilter 96 Plates, 4 TurboFilter 96 Plates, 1 x 100 ml Ni-NTA Superflow |
Product Details
In response to customers’ needs for larger amounts of protein from automated procedures, QIAGEN has adapted the Ni-NTA Superflow 96 BioRobot protocol to enable processing of larger culture volumes and purification of milligram amounts of His-tagged protein per well. Increasing the amount of Ni-NTA Superflow resin used in the procedure to 200 µl per well and an optimized lysis buffer formulation enables up to 25 ml (purification under native conditions) or 15 ml (purification under denaturing conditions) cultures to be processed (high-yield protocols). Cell cultures are transferred to 24-well blocks for processing. The corresponding increase in biomass can deliver in some cases up to 10 mg of pure His-tagged protein per well (see table and figure Milligram amounts of His-tagged proteins per well) allowing multiple assays to be carried out on the same batch of protein and reducing the total number of protein preps required, see also figure Automated expression clone screening. The single-step purification provides highly pure proteins over a wide range of yields, and purification of large protein complexes is possible.
| His-tagged protein | Total yield per well (µg)* | Protein concentration (mg/ml)† |
|---|---|---|
| Green fluorescent protein | 4000 | 6.0 |
| T7 RNA polymerase | 1000 | 1.4 |
| GroES | 300 | 0.4 |
| Chloramphenicol acetyltransferase | 2400 | 4.4 |
| GroEL | 740 | 1.0 |
| Tumor necrosis factor α | 1600 | 2.5 |
| GroES/GroEL | 1200 | 1.5 |
| Cpn-10 | 170 | 0.3 |
The QIAexpress Ni-NTA Protein Purification System, including the Ni-NTA Superflow 96 BioRobot Kit, is based on the remarkable selectivity of patented Ni-NTA (nickel-nitrilotriacetic acid) resin for proteins containing an affinity tag of six or morehistidine residues — the His tag. This technology allows one-step purification of almost any His-tagged protein from any expression system under native or denaturing conditions. NTA, which has four chelation sites for nickel ions, binds nickel more tightly than metal-chelating purification systems that only have three sites available for interaction with metal ions. The extra chelation site prevents nickel-ion leaching and results in a greater binding capacity and protein preparations with higher puritythan those obtained using other metal-chelating purification systems. The QIAexpress system can be used to purify His-tagged proteins from any expression system including baculovirus, mammalian cells, yeast, and bacteria. (See figure Protein purification with the Ni-NTA protein purification system).
The Ni-NTA Superflow 96 BioRobot Kit is for use with BioRobot 3000, 8000, or 9600 workstations. .
| Denaturants | Detergents | Reducing agents | Others | Salts | For long-term storage |
|---|---|---|---|---|---|
| 6 M Gu·HCl | 2% Triton X-100 | 20 mM β-ME | 50% glycerol | 4 M MgCl2 | Up to 30% ethanol |
| 8 M urea | 2% Tween 20 | 10 mM DTT | 20% ethanol | 5 mM CaCl2 | or 100 mM NaOH |
| 1% CHAPS | 20 mM TCEP | 20 mM imidazole | 2 M NaCl |
The QIAexpress Ni-NTA Protein Purification System provides reliable, one-step purification of proteins suitable for many application, including:
- Structural and functional investigations
- Crystallization for determination of three-dimensional structure
- Assays involving protein–protein and protein–DNA interactions
- Immunization to produce antibodies
Specifications
Features | Specifications |
| Applications | Proteomics |
| Bead size | 60–160 µm |
| Binding capacity | 5–20 mg/ml |
| Number of preps per run | 1–96 samples per run |
| Processing | Automated |
| Scale | Medium scale |
| Special feature | Cross-contamination-free |
| Start material | Cell lysate |
| Support/matrix | Superflow |
| Tag | 6xHis tag |
| Yield | 15 µg – 4 mg |
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