Minute TM Mitochondria Isolation Kit for Mammalian Cells and Tissues MP-007

Minute TM Mitochondria Isolation Kit for Mammalian Cells and Tissues(50 Tests)

Manual/protocol

MSDS sheet

Minute™ Mitochondria Isolation Kit for Mammalian Cells and Tissues is composed of optimized buffers and protein extraction filter cartridges with 2.0 ml collection tubes. The kit is designed to rapidly isolate native mitochondria proteins from cultured mammalian cells or tissues. Due to the use of protein extraction filter cartridges, the protein isolation procedure is simple and provides a high yield. The procedure can be completed in less than 30 minutes. Unlike many commercial mitochondria preparation kits, this kit offers a wide range of starting cells and isolated mitochondria. The buffers are detergent and EDTA free. A Dounce homogenizer or a tissue blender is not needed.

Figure 1. Enrichment of Mitochondrial Marker (Ubiquinol-Cytochrome C Reductase Core Protein) with Minute™ Mitochondria Isolation Kit. 

 A. SDS-PAGE profiles of total protein extract vs. isolated mitochondrial proteins. Lanes 1, 3, 5, total proteins from isolated mouse kidney cells, mouse skeletal muscle and liver tissues, respectively. Lanes 2, 4, 6, isolated mitochondrial proteins from mouse kidney cells, mouse skeletal muscle and liver tissues, respectively.

 B. Western blotting. Proteins in A were transferred to nitrocellulose membranes and probed with anti-ubiquinol-cytochrome C reductase core protein (ab96333, abcam, Cambridge, MA) and anti-lamin B1 (ab16048, a nuclear envelope marker protein. abcam, Cambridge, MA). 

 C. Densitometry measurement of mitochondrial marker signals.

Kit includes:

1. 
   
2. Chen, X. Y., Ren, H. H., Wang, D., Chen, Y., Qu, C. J., Pan, Z. H., ... & Li, D. F. (2019). Isoliquiritigenin Induces Mitochondrial Dysfunction and Apoptosis by Inhibiting mitoNEET in a Reactive Oxygen Species-Dependent Manner in A375 Human Melanoma Cells. Oxidative Medicine and Cellular Longevity, 2019.
3. Ma, J., Chen, L., He, X. X., Wang, Y. J., Yu, H. L., He, Z. X., ... & Zhu, X. J. (2019). Functional prediction and characterization of Dip2 gene in mice. Cell biology international.
4. Cai, M., He, P., & Fang, D. L. Hypoxia‑induced mitochondrial translocation of DNM1L increases mitochondrial fission and triggers mPTP opening in HCC cells via activation of HK2. Oncology Reports.
5. Guo, Z., Song, T., Xue, Z., Liu, P., Zhang, M., Zhang, X., & Zhang, Z. (2019). Using CETSA assay and a mathematical model to reveal dual Bcl-2/Mcl-1 inhibition and on-target mechanism for ABT-199 and S1. European Journal of Pharmaceutical Sciences, 105105.
6. Yue, J., Shen, Y., Liang, L., Cong, L., Guan, X., Li, Z., ... & Xu, W. In situ and ex situ surface‐enhanced Raman spectroscopy (SERS) analysis of cell mitochondria. Journal of Raman Spectroscopy.
7. Duan, C., Kuang, L., Xiang, X., Zhang, J., Zhu, Y., Wu, Y., ... & Li, T. (2020). Activated Drp1-mediated mitochondrial ROS influence the gut microbiome and intestinal barrier after hemorrhagic shock. Aging (Albany NY), 12(2), 1397.
8. Duan, C., Kuang, L., Xiang, X., Zhang, J., Zhu, Y., Wu, Y., ... & Li, T. (2020). Drp1 regulates mitochondrial dysfunction and dysregulated metabolism in ischemic injury via Clec16a-, BAX-, and GSH-pathways. Cell Death & Disease, 11(4), 1-19.
9. Han, W., Zhang, C., Shi, C. T., Gao, X. J., Zhou, M. H., Shao, Q. X., ... & Yuan, J. L. (2020). Roles of eIF3m in the tumorigenesis of triple negative breast cancer. Cancer Cell International, 20(1), 1-16.