Feces Homogenizer

Ideal for Feces Homogenization

Do you spend lots of time and effort homogenizing feces samples? The Bullet Blender® tissue homogenizer delivers high quality and superior yields. No other homogenizer comes close to delivering the Bullet Blender’s winning combination of top-quality performance and budget-friendly affordability. 

Save Time, Effort and Get Superior Results with

The Bullet Blender Homogenizer

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 Blender ever touches the tissue – the sample tubes are kept closed during homogenization. There are no probes to clean between samples.

Samples Stay Cool

The Bullet Blenders’ innovative and elegant design provides convective cooling of the samples, so they do not heat up more than several degrees. In fact, our Gold+ models hold the sample temperature to about 4ºC.

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

Thousands of peer-reviewed journal articles attest to the consistency and quality of the Bullet Blender homogenizer. We offer a 2 year warranty, extendable to 4 years, because our Bullet Blenders are reliable and last for many years.

What Else Can You Homogenize? Tough or Soft, No Problem! 

The Bullet Blender can process a wide range of samples including organ tissue, cell culture, plant tissue, and small organisms. You can homogenize samples as tough as mouse femur or for gentle applications such as tissue dissociation or organelle isolation.

the Bullet Blender high-throughput tissue homogenizer

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    Bullet Blender Models

    Select Publications using the Bullet Blender to Homogenize Feces Tissue

    See all of our Bullet Blender publications!

    Lim, M. Y., Hong, S., Kim, B.-M., Ahn, Y., Kim, H.-J., & Nam, Y.-D. (2020). Changes in microbiome and metabolomic profiles of fecal samples stored with stabilizing solution at room temperature: a pilot study. Scientific Reports, 10(1), 1789. https://doi.org/10.1038/s41598-020-58719-8
    Lee, L.-C., Wei, L., Huang, W.-C., Hsu, Y.-J., Chen, Y.-M., & Huang, C.-C. (2015). Hypolipidemic Effect of Tomato Juice in Hamsters in High Cholesterol Diet-Induced Hyperlipidemia. Nutrients, 7(12), 10525–10537. https://doi.org/10.3390/nu7125552
    Marvin, S. A., Huerta, C. T., Sharp, B., Freiden, P., Cline, T. D., & Schultz-Cherry, S. (2015). Type I Interferon Response Limits Astrovirus Replication and Protects Against Increased Barrier Permeability in vitro and in vivo. Journal of Virology, JVI.02367-15. https://doi.org/10.1128/JVI.02367-15
    Mon, K. K. Z., Saelao, P., Halstead, M. M., Chanthavixay, G., Chang, H.-C., Garas, L., Maga, E. A., & Zhou, H. (2015). Salmonella enterica Serovars Enteritidis Infection Alters the Indigenous Microbiota Diversity in Young Layer Chicks. Frontiers in Veterinary Science, 2. https://doi.org/10.3389/fvets.2015.00061
    Rand, M. D., Vorojeikina, D., van Wijngaarden, E., Jackson, B. P., Scrimale, T., Zareba, G., Love, T. M., Myers, G. J., & Watson, G. E. (2015). Methods for Individualized Determination of Methylmercury Elimination Rate and De-Methylation Status in Humans Following Fish Consumption. Toxicological Sciences, kfv241. https://doi.org/10.1093/toxsci/kfv241
    Ranjan, R., Rani, A., Metwally, A., McGee, H. S., & Perkins, D. L. (2015). Analysis of the microbiome: Advantages of whole genome shotgun versus 16S amplicon sequencing. Biochemical and Biophysical Research Communications. https://doi.org/10.1016/j.bbrc.2015.12.083
    Andersson, S., Sikora, P., Karlberg, M. L., Winiecka-Krusnell, J., Alm, E., Beser, J., & Arrighi, R. B. G. (2015). It’s a dirty job — A robust method for the purification and de novo genome assembly of Cryptosporidium from clinical material. Journal of Microbiological Methods, 113, 10–12. https://doi.org/10.1016/j.mimet.2015.03.018
    Goodrich, K. M., Smithson, A. T., Ickes, A. K., & Neilson, A. P. (2015). Pan-colonic pharmacokinetics of catechins and procyanidins in male Sprague–Dawley rats. The Journal of Nutritional Biochemistry. https://doi.org/10.1016/j.jnutbio.2015.04.008
    Lakritz, J. R., Poutahidis, T., Levkovich, T., Varian, B. J., Ibrahim, Y. M., Chatzigiagkos, A., Mirabal, S., Alm, E. J., & Erdman, S. E. (2014). Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice: Probiotic bacteria protect against mammary cancer. International Journal of Cancer, 135(3), 529–540. https://doi.org/10.1002/ijc.28702
    Araújo-Pérez, F., McCoy, A. N., Okechukwu, C., Carroll, I. M., Smith, K. M., Jeremiah, K., Sandler, R. S., Asher, G. N., & Keku, T. O. (2012). Differences in microbial signatures between rectal mucosal biopsies and rectal swabs. Gut Microbes, 3(6), 530–535. https://doi.org/10.4161/gmic.22157
    Topal, E. (2010). Subunit vaccine to prevent Escherichia coli O157LH7 intestinal attachment and colonization. Arizona State University.

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