Protino Ni-NTA Agarose (100 mL)

Catalog nr. 745400100
Macherey-Nagel

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Sale price€1.015,00
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Description

Protino Ni-NTA Agarose (100 mL) is a Ni-NTA suspension on settled beaded agarose for the purification of His-tag proteins in biochromatography workflows. The ready suspension format supports affinity capture of polyhistidine-tagged targets from expression lysates and related sample matrices under standard laboratory purification protocols. This pack provides 100 mL of settled beaded agarose, suited to method development, scale-up trials and routine preparative work where nickel-NTA chemistry is established. Protino Ni-NTA Agarose from manufacturer Macherey-Nagel is positioned among reagents for biochromatography and is described as not classified as dangerous goods under transport regulations. Laboratories use the material for immobilised-metal affinity steps prior to elution, buffer exchange or downstream analysis. The settled beaded agarose matrix offers a practical handling form for column or batch formats commonly applied to His-tag protein isolation. Choose this 100 mL pack when a defined settled-bed volume of Ni-NTA agarose is required for His-tagged protein purification.

This article is part of Sorbents, silica gel & ion exchangers, in SPE & sample preparation.

Key features

  • Pack size: 100 ml
  • Storage temperature: 6 - 7 °C
  • Product: Protino Ni-NTA Agarose suspension
  • EAN: 4046681153204
  • Technical Information Sheet: PDF
  • Safety Data Sheet: PDF

Compliance & Safety Information

GHS02, flammableGHS07, harmfulWarning

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Questions about Protino Ni-NTA Agarose (100 mL)

What is this article?

Protino Ni-NTA Agarose (100 mL) is the article on this page. Luminix Health distributes Macherey-Nagel for laboratory use. It sits in Sorbents, silica gel & ion exchangers, inside SPE & sample preparation, in Chromatography equipment.

Loose sorbent, silica gel and ion-exchange resin are the phases bought in bulk to pack a column or to stir into a solution. Particle size and activity, or the ion-exchange capacity, are the specification. A TLC silica and a flash silica of different particle sizes are not the same separation.

Solid-phase extraction holds a compound on a sorbent while the rest of the sample is washed away, then releases it in a small volume. The sorbent, the bed mass and the solvents are the method. Silica, ion exchangers and polymer phases do different jobs. A flash column is the same idea scaled toward purification rather than trace cleanup. The molecules are on PubChem, named by IUPAC.

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