Tissue dissociation

Ideal for Tissue Dissociation

Save Time, Effort and Get Superior Results with

Bullet Blender Homogenizer
  • Consistent Results
  • Samples Stay Cool
  • No Cross Contamination
  • Easy and Convenient
  • Risk Free
Do you spend lots of time and effort homogenizing tissue samples? The Bullet BlenderĀ® is a multi-sample homogenizer that delivers superior results. No other homogenizer comes close to delivering the Bullet Blender’s winning combination of top-quality performance and budget-friendly affordability.
  • Consistent and High Yield Results
    Run up to 24 samples at the same time under microprocessor-controlled conditions, ensuring experimental reproducibility and high yield. Process samples from 10mg or less up to 3.5g.
  • No Cross Contamination
    No part of the Bullet BlenderĀ® ever touches the tissue – the sample tubes are kept closed during homogenization. There are no probes to clean between samples.
  • Samples Stay Cool
    Homogenizing causes only a few degrees of heating. Our “Blue” model comes with a fan to maintain ambient temperatures.
  • Easy and Convenient to Use
    Just place beads and buffer along with your tissue sample in standard tubes, load tubes directly in the Bullet Blender, select time and speed, and press start.
  • Risk Free Purchase
    The Bullet BlenderĀ® comes with a 30 day money back guarantee and a 2 year warranty, with a 3 year warranty on the motor. The simple, reliable design enables the Bullet Blenders to sell for a fraction of the price of ultrasonic or other agitation based instruments, yet provides an easier, quicker technique.

 

 

Bullet Blender settings for Tissue Dissociation

Sample size

See the Protocol

microcentrifuge tube model (up to 300 mg) Small spleen samples for generation of splenocytes

 

Selected publications for Tissue Dissociation

See all of our Bullet Blender publications!

Booth, J. S., Salerno-Goncalves, R., Blanchard, T. G., Patil, S. A., Kader, H. A., Safta, A. M., Morningstar, L. M., Czinn, S. J., Greenwald, B. D., & Sztein, M. B. (2015). Mucosal-Associated Invariant T Cells in the Human Gastric Mucosa and Blood: Role in Helicobacter pylori Infection. Frontiers in Immunology, 6. https://doi.org/10.3389/fimmu.2015.00466
Booth, J. S., Toapanta, F. R., Salerno-Goncalves, R., Patil, S., Kader, H. A., Safta, A. M., Czinn, S. J., Greenwald, B. D., & Sztein, M. B. (2014). Characterization and Functional Properties of Gastric Tissue-Resident Memory T Cells from Children, Adults, and the Elderly. Frontiers in Immunology, 5. https://doi.org/10.3389/fimmu.2014.00294
Wiedner, S. D., Ansong, C., Webb-Robertson, B.-J., Pederson, L. M., Fortuin, S., Hofstad, B. A., Shukla, A. K., Panisko, E. A., Smith, R. D., & Wright, A. T. (2013). Disparate Proteome Responses of Pathogenic and Nonpathogenic Aspergilli to Human Serum Measured by Activity-Based Protein Profiling (ABPP). Molecular & Cellular Proteomics, 12(7), 1791–1805. https://doi.org/10.1074/mcp.M112.026534
Kim, K.-T., Zaikova, T., Hutchison, J. E., & Tanguay, R. L. (2013). Gold Nanoparticles Disrupt Zebrafish Eye Development and Pigmentation. Toxicological Sciences, 133(2), 275–288. https://doi.org/10.1093/toxsci/kft081
von Alvensleben, N., Stookey, K., Magnusson, M., & Heimann, K. (2013). Salinity Tolerance of Picochlorum atomus and the Use of Salinity for Contamination Control by the Freshwater Cyanobacterium Pseudanabaena limnetica. PLoS ONE, 8(5), e63569. https://doi.org/10.1371/journal.pone.0063569
Hong, N., De-Xing, Q., Deng-Xiang, Z., & Long-Zhong, R. (2012). A Simple Cultural Method for Detection of Mycoplasma bovis. Journal of Animal and Veterinary Advances, 11(10), 1643–1646. https://doi.org/10.3923/javaa.2012.1643.1646
Rayner, K. J., Suarez, Y., Davalos, A., Parathath, S., Fitzgerald, M. L., Tamehiro, N., Fisher, E. A., Moore, K. J., & Fernandez-Hernando, C. (2010). MiR-33 Contributes to the Regulation of Cholesterol Homeostasis. Science, 328(5985), 1570–1573. https://doi.org/10.1126/science.1189862
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