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ToxinEraser Endotoxin Removal Kit

AC
Catalog No. ABIN491524
  • Application
    Affinity Chromatography (AC)
    Brand
    ToxinEraser™
    Characteristics
    ToxinEraser is an endotoxin removal resin of high efficiency. It is based on the affinity matrix of modified polymyxin B (PMB), which allows highly efficient endotoxin removal. The final endotoxin level can be decreased to less than 0.1 EU/mL with repeat use of ToxinEraser endotoxin removal resin.
    • High stability and high removal efficiency
    • High binding capacity: > 2,000,000 EU/mL (CV)
    • Fast flow without any constant speed pump
    • Reusable up to five times if properly regenerated
    • Ready-to-use reagents and materials, such as equilibration buffer, collection tubes, etc.

    • Size: 1.5 mL in pre-packed column
    • Binding Capacity: Up to 2,000,000 EU/mL resin.
    • Ligand: Modified PMB (Polymixin B)
    • pH Stability: pH 5 -10
    • Support Matrix: 4% cross-linked agarose, spherical beads
    • Mean Particle Size: 90 μm
    • Equilibration Buffer: Phosphate-Buffer, pH 8.0
    • Types of substances that can be applied to the column: Protein, including peptides and antibody, polysaccharide etc.
    • Applicable Ionic Strength: 0.1 to 0.5 M NaCl
    • Substances tested that do not interfere with performance: 20% DMSO, 20% ethanol, 20% glycerol, 1 M urea, 300 mM imidazole, 0.05% Tween 20, 10 mM DTT, etc.
    Components
    • ToxinEraser Endotoxin Removal Resin: 1.5 mL pre-packed column
    • Regeneration Buffer: 125 mL
    • Equilibration Buffer: 125 mL
    • Collection Tubes: 1 pack (3 per pack)
    • Tips (1 mL): 2 packs (6 per pack)

    Equilibration buffer and regeneration buffer are separately available: ABIN769950, ABIN769949
    Material not included
    Column stand
    0.1 N sodium hydroxide or 0.1 N hydrochloric acid for adjusting the pH of the sample, and 3M NaCl for adjusting the ionic strength of the sample.
  • Sample Preparation

    Sample Preparation. pH and ionic strength of the samples are the main factors that affect the performance of the resin. In general, a pH of 7- 8 is optimal, although the binding of LPS to the resin occurs from pH 6 to 9. Proper ionic strength can reduce the nonspecific binding or the loss of protein. 0.15 - 0.5 M NaCl is recommended for high-efficiency endotoxin removal and lower sample loss.

    Restrictions
    For Research Use only
  • Handling Advice
    Do not freeze
    Storage
    4 °C
    Expiry Date
    18 months
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  • Background
    Lipopolysaccharide (LPS) is a bacterial endotoxin, and a major constituent of the cell walls of gram-negative bacteria. During gram-negative bacteremia or endotoxemia, LPS is the principal pathophysiological mediator by which bacteria can cause hypotension, organ failure, disseminated intravascular coagulation, and fatal shock in mammalian hosts. The removal of these endotoxins is highly necessary for downstream processes but also highly difficult.
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