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Agarose Chromatography Media: ... Ni Purerose TM 6 Fast Flow (IDA) Ni Purerose TM 6 Fast Flow (NTA) r-Protein A Purerose TM 4 Fast Flow:

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NTA is a tetravalent chelating agent, covalently coupled to cross-linked agarose beads, providing a higher specificity and lower ion leaching than IDA linked resins. NTA resins have also been shown to be more robust in the presence of higher concentrations of EDTA, but may require a higher imidazole concentration for protein elution.

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Kit contents: Qiagen Ni-NTA Magnetic Agarose Bead, 2 x 1mL, 20 to 70m Bead size, Up to 2mg/mL Suspension Binding Capacity, <10mg Protein/Column Yield, Cell Lysate Start Material, Automated/manual Processing, For High-throughput, Micro-scale Purification of His-tagged Proteins and Versatile Magnetocapture Assays using His tags, Includes Nickel ...

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NTA/His-Tag Agarose Beads: Lectin Coated Agarose Beads: ... AR-NTA-1: Ni-NTA His-select Agarose Beads: 4B: 10 mL: $485.00: AR-AZ-1: Agarose beads, azide functional: 5 ...

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Jan 01, 2002 · Development and characterization of Ni‐NTA‐bearing microspheres Development and characterization of Ni‐NTA‐bearing microspheres Lauer, Sabine A.; Nolan, John P. 2002-01-01 00:00:00 Because of its capacity to make sensitive and quantitative measurements with real‐time kinetic resolution without separating free from bound molecules, flow cytometry has recently begun to be recognized as ...

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Ni-NTA Magnetic Agarose Beads (2 x 1 ml) Price: Please Inquire. Condition: New. Thermo Owl Scientific Easycast B2 DNA Agarose Electrophoresis System 0-150v. Price ...

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Finden Sie eine große Auswahl an Proteinpurifikation -Produkten und erfahren Sie mehr über Macherey-Nagel™ Protino™ Ni-NTA Agarose: Proteinpurifikation Extraktion

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Ni-NTA agarose QIAgen 1 ml column with luer lock on both ends MoBiTec 10 ml luer lock syringe Merck Eurolab Buffer Composition Equilibration buffer 20 mM Tris/HCl, 200 mM NaCl; pH 7.5 Washing buffer 20 mM Tris/HCl, 200 mM NaCl, 5 mM imidazole; pH 7.5 Elution buffer 1* 20 mM Tris/HCl, 200 mM NaCl, 20 mM imidazole; pH 7.5

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The term Ni-NTA (Nickel NTA) refers to a nickel 2+ ion that has been coupled to Nitrilotriacetic acid (NTA). Ni-NTA can then be coupled to agarose resin or magnetic beads for IMAC (Immobilized Metal Chelate Affinity Chromatography). This is a purification method to obtain functional His-tagged protein.

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Application Area: Protein Purification " For purification of His-tagged proteins this is one of the best. The amount of the purified recombinant proteins containing a polyhistidine (6xHis) sequence using Ni-NTA Agarose by QIAGEN was great.

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Heparin, Ni-NTA, Co-NTA and Glu chemistries are supplied as High Performance resins with a mean bead size of 35 μ m. High selective binding capacity is the key benefit of Protein Ark's Super resins. Protein Ark's Fastback Resins include Protein A & G, Co IMAC, Ni IMAC chemistries.
Ni-NTA His•Bind® Superflow™ Resin is a medium-pressure compatible version of the Ni-NTA His•Bind® Resin (Cat. No. 70666). It has all the same characteristics, except the agarose matrix has a higher level of crosslinking for higher bead rigidity.
Ni-NTA Agarose is an affinity chromatography matrix for purifying recombinant proteins carrying a His tag. Histidine residues in the His tag bind to the vacant positions in the coordination sphere of the immobilized nickel ions with high specificity and affinity. Cleared cell lysates are loaded onto the matrices.
Application Area: Protein Purification " For purification of His-tagged proteins this is one of the best. The amount of the purified recombinant proteins containing a polyhistidine (6xHis) sequence using Ni-NTA Agarose by QIAGEN was great.
Ni-NTA Agarose is a nickel-charged affinity resin that can be used to purify recombinant proteins containing a polyhistidine (6xHis) sequence. Proteins bound to the resin may be eluted with either low pH buffer or by competition with imidazole or histidine. One-step purification can be performed under both native and denaturing conditions.

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The enzyme showed catalytic activity for transesterification reaction. Transesterification activity of immobilized lipase on Ni-NTA agarose was increased by three fold (75.04% conversion) compared to that the free enzyme (24.65%), while the activity of immobilized lipase on carboxymethyl chitosan was slightly decreased (19.86%).
The term Ni-NTA (Nickel NTA) refers to a nickel 2+ ion that has been coupled to Nitrilotriacetic acid (NTA). Ni-NTA can then be coupled to agarose resin or magnetic beads for IMAC (Immobilized Metal Chelate Affinity Chromatography). This is a purification method to obtain functional His-tagged protein. loaded on an Ni-NTA-agarose (Qiagen) column (1-ml bed volume) equilibrated with buffer A. To remove unbound and nonspecifically buffer A, 10 ml of buffer A without NaC1, and 10 ml of buffer A bound proteins, the column was washed sequentially with 25 ml of adjusted to pH 5.5. Highly purified HisUb was then eluted with 5 ml