Cleanascite™ Lipid Removal Reagent and Clarification

Cleanascite™ Lipid Removal Reagent and Clarification

A high binding capacity for lipids with minimal cross-reactivity with proteinsEffectively replaces chlorinated/fluorinated hydrocarbons (eg. freon) and it is environmentally friendly.Helps purify antibodies, recombinant proteins, nucleic acids, proteoglycansIdeal for clarifying ascites, serum, cell & tissue culture, bile and organ homogenatesClarifies saliva and fecal componentsVery low protein bindingDoes not bind to DNA, RNA, enzymes and proteinsLeaves glycoproteins, antibodies, nucleic acids, hemoglobin, proteoglycans, nucleic acids, serum components(such as hormones, nutrients, globulins, clotting factors, transport proteins) aloneExtends the life of membrane and chromatographic columns.Enrichment of delipidated tissue samplesIdeal for delipidation treatments for downstream processing of large-scale therapeutic proteins, enzymes and monoclonal antibodies.

Cleanascite™ selectively removes lipids, cell debris, lipoproteins, floating fats, impurities from cohn paste, transgenic milk, egg yolk and biological samples for pretreatment of samples prior to purification. The reagent is a solid-phase, non-ionic adsorbent supplied as a suspension in saline, ready for use. Simply add, centrifuge and/or filter. The clarified supernatant is ready for subsequent downstream processing or analysis.

For more information on Cleanascite™ X2555-4000, total sample volume that can be processed : 4 Liters, please contact us.

For more information on Cleanascite™ X2555-16000, total sample volume that can be processed : 16 Liters, please contact us.

Research Article Cites Cleanascite™ for Serum Diabetes Biomarkers
 
MONMOUTH JUNCTION, NJ, February 4, 2016 -- Biotech Support Group reports on a recent research article describing the simplicity and efficiency of their proteomic sample preparation technology for clearing lipid-associated matrix effects from human sera.
 
The citation is:
Steven W. Taylor, Nigel J. Clarke^, , Zhaohui Chen, Michael J. McPhaul. A high-throughput mass spectrometry assay to simultaneously measure intact insulin and C-peptide. Clinica Chimica Acta
Available online 25 January 2016.   doi:10.1016/j.cca.2016.01.019