ROTI®Garose-His/Ni NTA-Cartridges, for biochemistry, 1 unit(s), plastic

Catalog nr. 0804.1
Carl Roth

Volume: 1 pc(s)
Value Packs: 1 piece
Price:
Sale price€299,95
Ask quote for bulk order

Description

ROTI®Garose-His/Ni NTA-Cartridges, for biochemistry, Density (D) 0,85 to 0,95 g/cm³, Flash point (flp) >50 °C, Boiling point (bp) >80 °C, Storage temp. +4 °C, UN-Nr. 1170

For the isolation of His-tagged proteins under reducing conditions.Immobilized metal ion affinity chromatography (IMAC) still is the most widely used method to obtain high yield of very pure proteins with reasonable effort.ROTI®Garose His/Ni Beads and ready-to-use columns offer the perfect solution for your specific applications in the field of benchtop column chromatography, for protein isolation in batch processes or under medium pressures (MPLC, FPLC). Depending on the product, our beads are optimally suited for low or high flow rates or when small or large sample volumes are to be purified.

  • Superior recovery rate of pure His-tagged proteins
  • Minimized Nickel leaching
  • Compatible with denaturing and reducing reagents

The matrix of ROTI®Garose-His/Ni NTA products consists of crosslinked and beaded 6 % agarose, NTA-conjugated and charged with divalent Nickel ions. Nickel chelates recognize two histidines that are in close proximity and accessible with good specificity and very high affinity, making the Ni2+ charged matrix the first choice for all standard applications. The tetradentate NTA crosslinker enables highly efficient binding of His-tagged proteins and leads to high recovery rates with minimized nickel bleeding into the eluate.

Directions for use

ROTI®Garose-His/Ni NTA-Beads may be regenerated, making them very cost-effective.The Matrix is stable in all commonly used reagents including denaturing reagents (like 8 M urea, 6 M guanidinium hydrochloride) and (dependent on the respective buffer) reducing substances (for instance ≤30 mM glutathion, ≤10  mM DTT, ≤10 mM DTE, ≤20 mM β-mercaptoethanol und ≤0,3 % SDS).

Prepacked cartridges with Nickel charged NTA-agarose bead matrix for medium pressure affinity chromatography (MPLC) under reducing conditions.Immobilized metal ion affinity chromatography (IMAC) under medium pressure is the prefect method to obtain high yield of very pure proteins in minimum time. ROTI®Garose-His/Ni NTA-Cartridges offer the perfect solution for fast and simple isolation of His-tagged proteins from total lysates in reducing buffer solutions.Matrix in 15 % ethanol.

  • Very fast and simple purification of His-tagged proteins from total lysates
  • High binding capacity for 6×His-tagged protein
  • Recommended flow rate 5 ml/min
  • Standard ports 10-32 (1/16″)
  • Very versatile. Applicable with ÄKTA™FPLC™, pump and syringe
  • Reliable elution and regeneration
  • For medium pressure flow chromatography
Suitable for

ÄKTA™FPLC™ and for sample application via peristaltic pump or syringe.

Directions for use

ROTI®Garose His/Ni NTA-Cartridges are prepacked and may be used directly.Column material made from polypropylene and polyethylene (frit), Inner diameter 1,6 cm, height 2,5 cm, inlet port 10-32 (1/16″) female, outlet port 10-32 (1/16″) male.

Technical Information
Instructions for use, addition Prepacked columns, binding capacity 50-250 mg/column (His)6 

Compliance & Safety Information

GHS02, flammableGHS07, harmfulWarning

Hazard Statements (H-Phrases)

H226Flammable liquid and vapour. H319Causes serious eye irritation. EUH208Contains. May produce an allergic reaction.

Precautionary Statements (P-Phrases)

P210Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P280Wear protective gloves/protective clothing/eye protection/face protection. P303+P361+P353IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower]. P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

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