Description
ROTI®Garose-Protein A/G HPBeads are high-performance agarose beads for biochemistry and affinity chromatography, combining Protein A and Protein G binding functionalities on a single matrix. This dual-ligand format broadens immunoglobulin recognition and supports flexible antibody capture and purification strategies in research and preparative settings. Physical characteristics include a density of 0,85 to 0,95 g/cm³, a flash point above 50 °C and a boiling point above 80 °C, with classification under UN number 1170. It belongs to the bio-chromatography range used for affinity separations alongside related SEC and HIC techniques. Laboratories can apply the beads in column or batch formats for selective enrichment of antibodies and Fc-containing proteins. The compact presentation supports reproducible handling in protein biochemistry workflows that demand versatile Protein A/G-mediated binding performance.
This article is part of Sorbents, silica gel & ion exchangers, in SPE & sample preparation.
Key features
- Particle size: 50-150 µm
- Beads (cross-linked agarose): 4 %
- Ligand: recombinant protein A/G
- Chemical bonding: covalent
- Binding capacity (humane IgG): ~25 mg/ml
- Ethanol: 20 %
- Pack sizes: 0.5 ml, 1 ml, 2 ml
- Density: 0,85 to 0,95 g/cm³
- Flash point: >50 °C
- Boiling point: >80 °C
- Product type: Protein A/G HP agarose beads
- Technical Information Sheet:
- Safety Data Sheet:
Compliance & Safety Information
WarningHazard Statements (H-Phrases)
Precautionary Statements (P-Phrases)
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Questions about ROTI®Garose-Protein A/G HPBeads, for biochemistry, 0.5 ml, plastic
What is this article?
ROTI®Garose-Protein A/G HPBeads, for biochemistry, 0.5 ml, plastic is the article on this page. Luminix Health distributes Carl Roth 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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The category is SPE & sample preparation. The sub-category is Sorbents, silica gel & ion exchangers. The catalogue is Chromatography equipment.
Shelves beside this one are SPE cartridges & columns and Flash, empty & glass chromatography columns.
What should I check before I order?
The technical information on this page is the manufacturer's sheet. Read that, not a rewritten specification.
When this page shows a safety data sheet, use that manufacturer file. Hazard text does not belong in the sales description. For a pack size, a grade or a certificate that is not on the page, send a quote request or contact the team.
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Luminix Health distributes this article from the heart of Europe. Delivery across Europe, two to five days when in stock. Standard delivery is free from €250 excl. VAT. Cold-chain goods and dangerous goods under ADR are never included in that free delivery. The terms are in the Shipping Policy. The full brand index is on shop by brand. Who we are is on about us.
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