process hundreds or thousands of mitra microsamples per day
The Mitra® 96-Autorack™ enables any lab to process microsamples in a high throughput manner - whether for plate building or extracting multiple samples at one time, or both!
Mitra 96-autorack high throughput dbs processing

Our 96-Autoracks™ allow for the reformatting of Mitra® samples, for rapid accessioning and extraction. Experiment with a variety of extraction methods in multiple 96-Autoracks to quickly identify solvent combinations and agitation techniques that yield highest efficiencies.  These racks are compatible with 96-channel pipettors and liquid handling workstations like the INTEGRA VIAFLO. 

Fully loaded racks are compatible with standard 1 & 2 mL collection plates.
Barcodes adhered for tracking specimens.
Fully loaded with 96 microsamplers for easy method development.
Empty racks facilitate fast plate building with microsamplers removed from Clamshell or Cartridge formats.
Compatibility with liquid handling robotics allows rapid accessioning and extraction of microsamples.
Available in 10, 20, and 30 microliter volumes.

Common 96-Autorack Uses

Plate Building and Extractions 

With empty 96-Autoracks™, you can easily process incoming Mitra micorsamplers at scale. Barcoding is available to facilitate sample tracking.

 

Method Development

Experiment with a variety of extraction methods using fully loaded 96-Autoracks™ to quickly identify solvent combinations and agitation techniques that yield highest efficiencies.

 

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Fluid Compatibility

  • Blood
  • Serum
  • Tears
  • Cerebral spinal fluid (CSF)
  • Plasma
  • Urine
  • Synovial fluid
  • Saliva

2 Configurations to Select From

  1. Empty 
  2. Fully loaded with 96 microsamplers

Volumes Available (RSD < 4%)

10 µL  |  20 µL  |  30 µL



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Mitra® is an exempt medical device in the US, CE-IVD self-certified in the UK and EU, a Class 1 IVD in Australia, and registered with Health Canada. It is intended as a specimen collector and for the storage and transport of biological fluids. Use of the device with blood for diagnostic applications is limited to certain countries and, in the US, for research and non-diagnostic purposes only. Neoteryx Products are not marketed in the US for clinical diagnostic uses. In other countries, Neoteryx Products may be used in clinical diagnostic laboratory systems after the laboratory has validated their complete system in compliance with relevant rules and regulations. Neoteryx operates a Quality Management System (QMS) that is based on FDA good manufacturing practices, 21 CFR 820 regulations, and ISO-13485.

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