Exo-spin™ 96

Code Description Price Qty
EX07-96 Exo-spin™ 96 £895.00
Exo-spin 96 96-well exosome purification
Exo-spin™ 96 column plate

Product description

Exo-spin™ 96 provides proven size exclusion chromatography (SEC) mini-column (EX01) technology in a 96-well format, allowing up to 96 individual samples to be processed in less than 30 minutes. Sample volumes up to 0.5 ml can be purified. 

The kit provides flexibility with 8-column strips detachable from the plate, so you can process 8 samples in 8-column strips if needed

The Exo-spin™ 96 well product offers:

  • High-throughput exosome isolation at the benchtop in the standard 96 well format in under 30 minutes
  • Purify up to 0.5 ml of each sample
  • >97% of free proteins removed
  • Outstanding reproducibility +/- 5% Standard deviation, for consistent exosome purification, time after time
  • Flexibility to just work with single strips of 8 columns at a time
  • The convenience of purified exosomes eluted directly into a 96 well plate ready for high throughput downstream applications

The Exo-spin™ 96 can be used to isolate exosomes directly from protein-rich samples such as sera and plasma. If required, you can concentrate the sample with your preferred concentration method (e.g. concentrator, precipitation buffer)  to isolate from large volumes of low-protein biofluids, such as cell culture medium, cerebral spinal fluid (CSF), and urine.

The EX07 Exo-spin™ kit has been developed to process up to 500 µl blood samples (plasma or sera using iterative loading

 

Which Exo-spin™ kit do I use for my plasma or sera samples?

 

 

 

Plasma and Sera Product Selection Guide

Sample Volume

isolation method

Exo-spin Kit

column bed length

< 500 µl Note 1 

SEC

EX03 mini columns

EX07 96-well

1.3 cm 

< 150 µl 

SEC

EX05  mini-HD 6.35 cm 
100 µl - 250 µl Note 2 concentration + SEC EX02 mini blood 1.3 cm  
1 ml SEC EX04 midi 2.15 cm 

Note 1: 
 Up to 250 µl may be used with concentration. Note 2: Up to 500 µl for sera.

Exo-spin™ column and resin pore size

The column bed volume in EX07 Exo-spin™ 96 plate is 500 µl. 100 µl of the sample may be loaded onto each column. Iterative loading allows up to 0.5 ml sera in total to be purified.

The pore size within the resin is approximatively 30 nm. Free molecules (e.g. proteins, lipids) which are smaller than 30 nm will enter into the pores within individual resin beads and their movement through the column is slower.

Highest recovery and purity

Blood plasma and sera typically contain around 1 x 1012 exosomes/ml. Size exclusion chromatography (SEC), provides a superior to technique to purify exosomes from blood. Samples can be added directly onto the column or concentrated, if required, prior to application. Exosomes in a range 30-250 nm will elute in the first fraction. >95% of free, non-exosomal proteins and lipids will be retained in the column and will elute later than the exosomes, ensuring a highly pure sample ready for downstream application.

Reproducibility

Reproducible purification provides the starting point to reproducible data. Exo-spin™ 96 columns provide excellent reproducibility with a standard deviation for exosome yield of just 5%. All Cell Guidance Systems columns are manufactured in our own manufacturing facility using advanced production techniques and quality control systems. This ensures the high reproducibility between each and every column within and between purification plates. A large number of peer-reviewed scientific papers have been published describing research which has been enabled by the use of Exo-spin™.

Storage

Upon receipt, store the kit at 4°C. 

Frequently Asked Questions (FAQs)

For any additional questions, please refer to FAQs document below.

If you are just starting to work with exosomes, you may wish to consider our starter pack

We designed the ideal starter pack to guide your exosome research. The starter pack includes the exosome purification kit of your choice, exosome validated antibodies and NTA profiling analysis. Complete details can be found in the product page here.

 

Product data

Exo-spin™ comparative data

Exosomes from blood plasma and sera
Exo-spin™ shows superior yield and purity. Data determined by nanoparticle tracking analysis (NTA). Each curve represents the average of 3 technical replicate measurements for each exosome isolation method and biofluid triplicate experiment. (PM = Precipitation Method). Data generated for Exo-spin mini columns which have the same resin and measurements. Adapted from (Martins, TS et al., 2018).

 

Exosomes NTA and EXOCET data
Data determined by NTA and EXOCET. Serum sample has been analysed for qualitative comparison between Exo-spin™ and precipitation methods. 

 

Characterizing Exo-spin™ 96 isolated exosomes using nanoparticle tracking analysis (NTA)

 

Exosome characterization with NTA. Excellent reproducibility is routinely achieved. Data for 8 columns shown. Exosomes have been isolated using Exo-spin™ 96 and analysis performed with the ZetaView® instrument.

Downstream applications: advice and content

The EX07 Exo-spin™ 96 kit is compatible with all downstream application and has been published in a large range of different applications.

RNA analysis:

  • Wang L., Wang C., Jia X. and Yu J. (2018). Circulating Exosomal miR-17 Inhibits the Induction of Regulatory T Cells via Suppressing TGFBR II Expression in Rheumatoid Arthritis. Cellular Physiology and Biochemistry; 50:1754–1763.
  • Emanueli C., Shearn AI., Laftah A., Fiorentino F., Reeves BC., Beltrami C., Mumford A., Clayton A., Gurney M., Shantikumar S. and Angelini G. (2016). Coronary Artery-Bypass-Graft Surgery Increases the Plasma Concentration of Exosomes Carrying a Cargo of Cardiac MicroRNAs: An Example of Exosome Trafficking Out of the Human Heart with Potential for Cardiac Biomarker Discovery. PLoS One 29;11(4):e0154274.

Mass Spectrometry:

  • Menezes-Neto A., Fidalgo Sáez MJ., Lozano-Ramos I., Segui-Barber J., Martin-Jaular L., Estanyol Ullate JM., Fernandez-Becerra C., Borrás FE., and del Portillo HA. (2015). Size-exclusion chromatography as a stand-alone methodology identifies novel markers in mass spectrometry analyses of plasma-derived vesicles from healthy individuals. Journal of Extracellular Vesicles; 4: 10.3402/jev.v4.27378.

Functional study:

  • Sheller-Miller S, Trivedi J, Yellon SM, and Menon R. (2019). Exosomes Cause Preterm Birth in Mice: Evidence for Paracrine Signaling in Pregnancy. Scientific Reports 24;9(1):608.

Citations

Sheller-Miller S, Trivedi J, Yellon SM, and Menon R. (2019). Exosomes Cause Preterm Birth in Mice: Evidence for Paracrine Signaling in Pregnancy. Scientific Reports 24;9(1):608.

Soares Martins, T., Catita, J., Martins Rosa, I., Cruz da Silva, O., and Henriques, A.G. (2018) Exosome isolation from distinct biofluids using precipitation and column-based approaches. PLoS One. 13(6):e0198820.

Wang L., Wang C., Jia X. and Yu J. (2018). Circulating Exosomal miR-17 Inhibits the Induction of Regulatory T Cells via Suppressing TGFBR II Expression in Rheumatoid Arthritis. Cellular Physiology and Biochemistry; 50:1754–1763.

Emanueli C., Shearn AI., Laftah A., Fiorentino F., Reeves BC., Beltrami C., Mumford A., Clayton A., Gurney M., Shantikumar S. and Angelini G. (2016). Coronary Artery-Bypass-Graft Surgery Increases the Plasma Concentration of Exosomes Carrying a Cargo of Cardiac MicroRNAs: An Example of Exosome Trafficking Out of the Human Heart with Potential for Cardiac Biomarker Discovery. PLoS One 29;11(4):e0154274

Menezes-Neto A., Fidalgo Sáez MJ., Lozano-Ramos I., Segui-Barber J., Martin-Jaular L., Estanyol Ullate JM., Fernandez-Becerra C., Borrás FE., and del Portillo HA. (2015). Size-exclusion chromatography as a stand-alone methodology identifies novel markers in mass spectrometry analyses of plasma-derived vesicles from healthy individuals. Journal of Extracellular Vesicles; 4: 10.3402/jev.v4.27378.