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Powering the future of diagnostics, delivering applications on the frontiers of medicine


       
 
RECENT NEWS
Ceres Nanosciences' scientist awarded Popular Science's "Brilliant 10" award for Nanotrap® work  view
Ceres Nanosciences awarded 250K to develop universal sample preparation tool for Rift Value Fever Virus
Press Release   view
Ceres Nanosciences releases publication on High Sensitivity Lyme Antigen Test in Biomaterials Journal
Publication   view
Ceres Nanosciences teams with Shimadzu and Nonlinear Dynamics to launch Nanotrap® Biomarker Discovery Platform
Press Release   view
In a Va. Lab, Forging Links To Speed Cancer Advances
The Washington Post   view

 

 

Ceres Nanosciences

Ceres Nanosciences provides breakthrough research platforms and diagnostic products using its unique and proprietary Nanotrap® capture particle technology. Ceres leverages the powerful Nanotrap® technology to meet the critical demands of the life sciences industry.    Learn more


SAMPLE PREP REAGENTS FOR R&D

Enhanced Sample Processing: Nanotrap® ESP Platform

Nanotrap® ESP Particles are a protein enrichment toolset optimized for a variety of assay platforms. Nanotrap® ESP Particles, developed from the Ceres proprietary Nanotrap® Platform technology, present a powerful and flexible toolset for research targeting the discovery and quantification of known and unknown low abundance peptides and proteins present in a range of complex biofluid matrices including cell culture supernatant, serum, urine, saliva, and cerebrospinal fluid.    Discover & Purchase


INNOVATIVE DIAGNOSTIC SOLUTIONS

Nanotrap® High Sensitivity Lyme Antigen Test

The Ceres' Nanotrap® High Sensitivity Lyme Antigen Test uses the Nanotrap® technology to directly measure Lyme antigens in urine using a Western Blot format. The Nanotrap® test is designed to provide high sensitivity and accuracy, delivering confident results at the earliest stages of infection. The Nanotrap® Lyme test is currently undergoing clinical trials. Anticipated clincial availabilty in late 2013 and early 2014.    Learn More


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