Revolutionizing High-Throughput Biological Sample Purification
100x increase in efficiency with preparative electrophoresis-in-microplates
Revolutionizing High-Throughput Biological Sample Purification
100x increase in efficiency with preparative electrophoresis-in-microplates
To help accelerate breakthroughs in diagnoses and treatment of cancer, dementia, senescence, genetic diseases …
The above steps are performed in parallel for up to 96 samples in 15-30 minutes.
Purification and QC analysis can be performed on DNA reactions, for example, transposase-based NGS library preps, or on protein preparations, for example, in vitro transcription-translation reactions.
The typical 20+ pipetting operations required for purifying reaction products by column- or bead-based approaches on a liquid-handling robot are reduced to just 2 pipetting operations, substantially reducing operational overheads, liquid and plastic waste, hands-on interventions and data management and sample tracking burdens.
Run times are reduced from the typical 360+ mins to < 30 mins enabling the processing of 10x more samples per unit time resulting in substantial efficiency and cost benefits.
The Axor system uses high-resolution electropheresis based purification ensuring consistent separation and purification, minimizing variability, and enabling the purification of even closely related species. Metrics that are challenging to achieve with binding-based purification methods.
The PEM electrophoresis microplate is made up of 12 strips with each strip containing 8 independent electrophoresis cells.
Each cell within the strip is isolated from every other cell avoiding cross contamination and allowing different purification parameters to be used for each sample. For example, for purification of an NGS library, different samples can be be assigned a different molecular weight range for purification.
The strips are application specific - for protein analysis only, for protein purification only, for DNA purifications only. Within a run, different strips can be combined, that is, a run may consist of 4 protein reaction purification strips and 8 DNA reaction purification strips or any other combination.
The strips are read-to-use with preloaded buffers and separation matrices enabling simple load-and-go operations.