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Capturem IP and Co-IP kit

Collection: Protein Expression & Purification

ÄKTA purification systems, His60 and Capturem his-tag tools, and CrystalQuick crystallization plates — Cytiva, Takara Bio, and Greiner in Israel.

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245 products

SE660 Tall Standard Dual Cooled Vertical Protein Electrophoresis Unit SE660-15-1.5 - Hoefer Inc.

Protein Electrophoresis

SE660 Tall Standard Dual Cooled Vertical Protein Electrophoresis Unit

Regular price From 8,616.00 NIS
Sale price Regular price
TE42 Standard Transfer Tank TE42 - Hoefer Inc.

Blotting

TE42 Standard Transfer Tank

Regular price 6,472.00 NIS
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CRYSTALQUICK RW PLATE, 96 WELL, ROUND WELLS - COC / Lbr, Concave Bottom - Greiner Bio-One (609820)

Protein Crystallisation

CRYSTALQUICK RW PLATE, 96 WELL, ROUND WELLS

Regular price 0.00 NIS
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CRYSTALQUICK LP PLATE, 96 WELL, SQUARE WELLS, FLAT BOTTOM, LOW PROFILE - COC / Lbr - Greiner Bio-One (609871)

Protein Crystallisation

CRYSTALQUICK LP PLATE, 96 WELL, SQUARE WELLS, FLAT BOTTOM, LOW PROFILE

Regular price From 0.00 NIS
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Biacore™ T200 GoldSeal 29003121 - Uncategorized - Cytiva

Uncategorized

pGEX Vectors

Regular price From 4,358.00 NIS
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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.

Buying Guide

Anchor the workflow on the tag: choose Capturem spin formats for speed, His60 gravity columns for economy, or HisTrap columns on an ÄKTA system for reproducible gradient elution, adding a Superdex size-exclusion polish for structural or interaction work. For protein-interaction screening, Takara's Matchmaker Gold yeast two-hybrid system covers library-scale screens, and CrystalQuick plates handle high-throughput crystallization. Prepacked columns and resins beyond the his-tag workflow live in our Chromatography Columns & Resins category.