Golgi apparatus enrichment made easy – Invent Biotechnologies Inc.

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Minute™ Golgi Apparatus Enrichment Kit (20 Preps)

Catalog Number: GO-037

  • $498.00



Manual & Protocol | MSDS

Golgi apparatus, also called Golgi complex or Golgi body, is made up of a series of flattened stacked pouches (cisternae). Golgi apparatus is a vital organelle in eukaryotic cells and is responsible for transporting, modifying, and packaging protein and lipids into vesicles for delivery to targeted locations.  The quantity and distribution of Golgi in different cell and tissue types vary significantly. The ability to obtain highly-enriched Golgi fraction is an important first step for studying its function and interaction with other organelles. Traditional methods for isolating Golgi apparatus are based on density gradient ultracentrifugation. The protocol requires a large amount of starting material and the methods are tedious and time-consuming. Unlike any other Golgi isolation kit, this kit uses a patented spin-column-based technology that is simple, rapid and requires only a small amount of starting material. This kit can preferentially enrich native Golgi by precipitation without using a Dounce homogenizer and ultracentrifugation. Two sub-Golgi fractions can be obtained: Golgi apparatus and secretory vesicles of Golgi.

Compare with Other Golgi Apparatus Enrichment Kits

Kit Components:

Items

Quantity

Buffer A

20 ml

Buffer B

8 ml

Buffer C

2 ml

Buffer D 2 ml

Plastic Rods

2 units

Filter Cartridge

20 units

Collection Tubes

20 units

1. Tan, X., Shi, L., Banerjee, P., Liu, X., Guo, H. F., Yu, J., ... & Creighton, C. J. (2020). A pro-tumorigenic secretory pathway activated by p53 deficiency in lung adenocarcinoma. The Journal of Clinical Investigation.

2. Zhu, Y., Shao, F., Yan, W., Xu, Q., & Sun, Y. (2020). Inhibition of SHP2 ameliorates psoriasis by decreasing TLR7 endosome localization. medRxiv.

3. Lita, A., Pliss, A., Kuzmin, A., Yamasaki, T., Zhang, L., Dowdy, T., ... & Larion, M. (2021). IDH1 mutations induce organelle defects via dysregulated phospholipids. Nature Communications12(1), 1-16.

4. Tan, X., Banerjee, P., Shi, L., Xiao, G. Y., Rodriguez, B. L., Grzeskowiak, C. L., ... & Kurie, J. M. (2021). p53 loss activates prometastatic secretory vesicle biogenesis in the Golgi. Science Advances7(25), eabf4885.

5.  Tan, X., Banerjee, P., Liu, X., Yu, J., Lee, S., Ahn, Y. H., ... & Kurie, J. M. (2021). Transcriptional control of a collagen deposition and adhesion process that promotes lung adenocarcinoma growth and metastasis. JCI insight.

6.  Zhang, L., Li, R., Geng, R., Wang, L., Chen, X. X., Qiao, S., & Zhang, G. (2022). Tumor Susceptibility Gene 101 (TSG101) Contributes to Virion Formation of Porcine Reproductive and Respiratory Syndrome Virus via Interaction with the Nucleocapsid (N) Protein along with the Early Secretory Pathway. Journal of Virology, jvi-00005.

7.  Huang, F., Tang, X., Ye, B., Wu, S., & Ding, K. (2022). PSL-LCCL: a resource for subcellular protein localization in liver cancer cell line SK_HEP1. Database2022.

8.  Mondal, T., Shivange, G., Habieb, A., & Tushir-Singh, J. (2022). A Feasible Alternative Strategy Targeting Furin Disrupts SARS-CoV-2 Infection Cycle. Microbiology Spectrum10(1), e02364-21.

9.  Zhu, Y., Wu, Z., Yan, W., Shao, F., Ke, B., Jiang, X., ... & Sun, Y. (2022). Allosteric inhibition of SHP2 uncovers aberrant TLR7 trafficking in aggravating psoriasis. EMBO molecular medicine14(3), e14455.

10.  Zhong, W., Lin, W., Yang, Y., Chen, D., Cao, X., Xu, M., ... & Yan, D. (2022). An acquired phosphatidylinositol 4-phosphate transport initiates T-cell deterioration and leukemogenesis. Nature Communications, 13(1), 1-18.

 

 



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