EndotoxinOUT™ (3 Citations)

EndotoxinOUT™ was designed for the rapid removal of endotoxins and pyrogens (LPS, lipopolysaccharides) from nucleic acid (DNA) samples. EndotoxinOUT™ is an ideal product for the cleanup of buffers, cell culture media, protein solutions, nucleic acid (DNA) samples and pharmacological components.
EndotoxinOUT™ consists of 6% cross-linked agarose covalently linked to polymyxin B to bind and remove harmful pyrogens from a solution. Polymyxin B is a family, polymyxin B1 and B2, of antibiotics that bind to the negatively charged site of the lipid A portion of the bacterial lipopolysaccharide layer, neutralizing the endotoxic activity. The covalently coupled agarose and polymyxin B is a stable matrix that resists leaching.
EndotoxinOUT™ kit is supplied with a regneration buffer, endotoxin free water and 5 x 1ml columns.
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Features
- Polymyxin B Sulfate immobilized on 6% cross-linked agarose
- Capacity: =9995 endotoxin units (EU) removed by 1ml resin from 5ml test containing 10,000EU
- Minimal leaching
- Reusable at least 10 times
Applications
- Cleanup of buffers, cell culture media, protein solutions, DNA samples & pharmacological components
- Rapid 99.95% removal of endotoxins & pyrogens from samples
Protocol | |
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Material Safety Data Sheet | |
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Technical Literature | |
Protein Purification Handbook | |
Sample Preparation Handbook | For Lysis Buffers, Fractionation, Dialysis, Protein Concentration and Enrichment |
Certificate Of Analysis | |
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- Terauchi, N., Meng, D., Li, W. et al. Fibroblast-activating potency of a hydrolysate of purified collagen and a tissue hydrolysate from sturgeon skin. Fish Sci 89, 527–535 (2023). https://doi.org/10.1007/s12562-023-01696-4
- Faouzi, Malika et al (2022) Acidic Cannabinoids Suppress Proinflammatory Cytokine Release by Blocking Store-operated Calcium Entry. FUNCTION. https://doi.org/10.1093/function/zqac033
- Hongxia, L. et al (2021) Identification, expression and pro-inflammatory effect of interleukin-17 N in common carp (Cyprinus carpio L.). Fish Shellfish Immunol. doi.org/10.1016/j.fsi.2020.11.024