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Protein analysis equipment and supplies
Vivaspin protein concentrator spin columns
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Protein analysis equipment and supplies
Sera-Mag™ Carboxylate-Modified Magnetic Beads & SpeedBeads
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Capturem™ His-Tagged Purification Miniprep Kit
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Protein analysis equipment and supplies
Sera-Mag™ SpeedBeads protein A/G magnetic particles
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Protein analysis equipment and supplies
His Mag Sepharose™ Ni
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B. Subtilis Secretory Protein Expression System
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Protein analysis equipment and supplies
NHS Mag Sepharose™
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Frequently asked questions
What is the difference between Ni-IDA and Ni-NTA resins for his-tag purification?
Both chelate nickel to capture polyhistidine tags; IDA holds the metal with three coordination sites and NTA with four. Takara's His60 Ni is a Ni-IDA resin with a 60 mg/ml binding capacity for one-step capture from bacterial, mammalian, or baculovirus lysates, while Cytiva's HisTrap HP columns come prepacked with Ni Sepharose HP. Imidazole gradients need re-optimizing whenever you switch resin chemistry.
Can I purify a his-tagged protein without an FPLC system?
Yes — gravity-flow columns, magnetic beads, and membrane-based spin formats all work at bench scale. Takara's Capturem kits capture his-tagged protein on a nickel-charged membrane in a standard centrifuge, going from clarified lysate or culture supernatant to purified protein in minutes, in miniprep, maxiprep, and 96-well formats.
In what order should I combine chromatography steps?
The standard strategy is capture, intermediate purification, polish: an affinity step such as HisTrap does the heavy lifting, ion exchange removes closely related contaminants when needed, and size exclusion — Superdex, for example — clears aggregates and exchanges buffer. Sephadex desalting columns bridge steps when buffers must change.
When is it worth moving up to an ÄKTA system?
When reproducibility, gradient control, or documentation start to matter — an ÄKTA go runs programmed methods with UV and conductivity monitoring in a footprint that fits a cold cabinet, which manual gravity columns cannot match. Labs purifying the same construct repeatedly usually recoup the bench time quickly.
Should I use sitting drop or hanging drop plates for protein crystallization?
Both are vapor-diffusion methods; sitting drop is easier to automate and gentler on fragile drops, while hanging drop simplifies crystal retrieval. Greiner's 96-well CrystalQuick plates run sitting-drop screens with three wells per reservoir — 288 conditions per plate — and the CrystalDrop lid lets one plate serve both geometries.
Who supplies protein purification systems and columns in Israel?
Danyel Biotech is the official Israeli distributor for the Cytiva, Takara Bio, and Greiner Bio-One protein-research lines — ÄKTA instruments, his-tag purification kits, and crystallization plates ship with local support and fast quotations.

