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Generate high-quality single-cell suspensions from mouse liver tissue efficiently and reliably using the STEMprep™ Mouse Liver Dissociation Kit. Designed to work seamlessly with the STEMprep™ Tissue Dissociator, this kit features a precisely formulated enzymatic cocktail tailored for liver tissue, combined with an optimized mechanical dissociation protocol to gently dissociate liver tissue while preserving cell viability and surface marker integrity.
The process is specifically designed to yield high numbers of non-parenchymal cells, including liver sinusoidal endothelial cells (LSECs) and Kupffer cells. By combining enzymatic digestion of the extracellular matrix with controlled mechanical dissociation, this method ensures consistent results with minimal hands-on time and user variability.
After dissociation, the cell suspension can be easily filtered and optionally treated with a debris removal step to improve sample purity. The resulting single-cell suspension is immediately suitable for downstream applications such as cell separation, culture, flow cytometry, and functional, genetic, or proteomic studies.
For best results, use this kit in conjunction with the STEMprep™ Tissue Dissociator and STEMprep™ Sample Tubes.
For more information on STEMprep™, visit the STEMprep™ overview page. Additionally, explore our instrumentation overview page or download our to learn more about available service options, including warranty coverage and additional support packages.
Figure 1. STEMprep™ Mouse Liver Dissociation Kit Achieves High Cell Viability and Consistent Yield
Mouse liver tissue was processed into single-cell suspensions using the STEMprep™ Mouse Liver Dissociation Kit and the STEMprep™ Tissue Dissociator or an alternative automated system. (A) Viability of total nucleated cells. (B) Yield of viable cells per whole liver tissue (900 - 2000 mg). (C and D) Proportion and yield of CD31+ liver sinusoidal endothelial cells and F4/80+CLEC4F+ Kupffer cells. Viability, yield, and subset composition were assessed by flow cytometry. Red blood cells were lysed with ammonium chloride solution before subset analysis. Data are presented as mean ± SD (n = 15 - 37).
Figure 2. STEMprep™-Processed Mouse Kupffer Cells Maintain Phagocytic Function
Mouse liver tissue was dissociated into single-cell suspensions using the STEMprep™ Mouse Liver Dissociation Kit and the STEMprep™ Tissue Dissociator, or an alternative automated system. (A) Kupffer cells were isolated from the single-cell suspensions using the EasySep™ Mouse F4/80 Positive Selection Kit. (B) The isolated F4/80+CLEC4F+ cells were incubated for 2h in the presence of pHrodo™ Green-conjugated E. coli BioParticles™ (BP) at 2 - 8°C (Cold) or 37°C. The fluorescence of phagocytosed BP was measured by flow cytometry. Data are presented as mean ± SD (n = 6).
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