Detergent-Free Protein Extraction Kit Spin Column Based – Invent Biotechnologies Inc.

Have a question? Ask our scientists!

{formbuilder:58797}

Minute™ Detergent-Free Protein Extraction Kit for Animal Tissues and Cultured Cells(50 Preps)

Read more literature references here

Catalog Number: SN-006

  • $450.00
Shipping calculated at checkout.



 

Manual & Protocol | Material Safety Data Sheets (MSDS)

Minute™ Detergent-Free Total Protein Extraction Kit is composed of optimized cell lysis buffer and protein extraction filter cartridges with 2.0 ml collection tubes. The kit is designed to quickly extract detergent-free total proteins from cultured cells (insect/mammalian/other cultured cells) and animal tissues. The protein extraction buffers do not contain any detergent and EDTA. The extraction volume can be as small as 20 μl and as large as 500 μl with the use of the protein extraction filter cartridges. When available starting material is a limiting factor, this can be quite useful. Detergent-free total proteins can be extracted from cultured cells/tissues in less than 5 minutes with high yield (1-5 mg/ml).

Figure 1. Comparison of protein profiles of different animal tissues extracted by denaturing lysis buffer and detergent-free extraction buffer. Lane 1: Drosophila cultured cells (SL2); Lane 2: Adult Drosophila flies; Lane 3: Gold fish muscle; Lane 4: Mouse liver. Extracted proteins were seperated in 10% SDS-PAGE and stained with Comassie blue.

Kit includes:

Items

Quantity

Buffer A

15 ml

Buffer B

15 ml

Protein Extraction Filter Cartridges

50 units

Collection Tubes with Cap

50 units

Plastic Rods

2 units

 

  1. Seo, J-H. et al (2014). Directing stem cell differenciation by changing the molecular mobility of supramolecular surfaces. Advanced Healthcare Materials. DOI: 10.1002/adhm.201400173
  2. M. Takada, S. Chiba et al. ((2015). Inflammatory responses to neutral fat and fatty acids in multiple organs in a rat model of fat embolism syndrome, Forensic Science International http://dx.doi.org/10.1016/j.forsciint.2015.07.011
  3. Seo J. et al. (2016). Dynamic polyrotaxane-coated surface for effective differentiation of mouse induced pluripotent stem cells into cardiomyocytes. RSC Advances. DOI: 10.1039/C6RA03967G.
  4. Xu, Wenteng, et al. (2016)."Ubiquitin ligase gene neurl3 plays a role in spermatogenesis of half-smooth tongue sole (Cynoglossus semilaevis) by regulating testis protein ubiquitination." Gene.
  5. Yamamoto, H., Hayano, S., Okuno, Y., Onoda, A., Kato, K., Nagai, N., ... & Kato, T. (2020). Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect. International Journal of Cardiology.
  6. Pietras, P., Leśniczak-Staszak, M., Kasprzak, A., Andrzejewska, M., Jopek, K., Sowiński, M., ... & Szaflarski, W. (2021). MVP Expression Facilitates Tumor Cell Proliferation and Migration Supporting the Metastasis of Colorectal Cancer Cells. International Journal of Molecular Sciences22(22), 12121.
  7. Minerva, D., Othman, N. L., Nakazawa, T., Ito, Y., Yoshida, M., Goto, A., & Suzuki, T. (2022). A New Chemotactic Mechanism Governs Long-Range Angiogenesis Induced by Patching an Arterial Graft into a Vein. International Journal of Molecular Sciences, 23(19), 11208.
  8. Leśniczak-Staszak, M., Pietras, P., Ruciński, M., Johnston, R., Sowiński, M., Andrzejewska, M., ... & Szaflarski, W. (2024). Stress granule-mediated sequestration of EGR1 mRNAs correlates with lomustine-induced cell death prevention. Journal of Cell Science, 137(12).


We Also Recommend