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Minute™ Adipose Tissue Fractionation Kit (20 Preps)

Minute™ Adipose Tissue Fractionation Kit (20 Preps)

Catalog Number: AF-023

  • $298.00


Manual & Protocol | Material Safety Data Sheets (MSDS)

On average, total cellular proteins account for less than 2% of adipose tissue. Adipose tissue, especially white adipose tissue, has been recognized as an important endocrine and inflammation organ in addition to its energy storage function. Fractionation and analysis of proteins from adipose tissue are critical for understanding many physiological/pathological conditions. However, fractionation of adipose tissue is challenging due to its high lipid and low protein contents. The water-oil emulsion present in biological samples is notoriously difficult to separate, but we have developed a cutting-edge technology to deal with this issue: a porous filter with unique surface property and predefined pore size coupling that has a specially formulated detergent-free fractionation buffer. This is the key to fractionating adipose tissue into two: water-soluble protein fraction and water insoluble fraction. The buffers used in this kit are free of primary amine, detergent and reducing agents. Isolated proteins are compatible with all downstream applications including TMT labeling, enzyme digestion, MS analysis and other applications.


A. SDS-PAGE (10%) profiles of fractionated adipose tissues. Lane 1, water-soluble fraction of porcine WAT; Lane 2, water-insoluble fraction porcine WAT; Lane 3, water-soluble fraction of rat WAT; Lane 4, a water-insoluble fraction of rat WAT.

B. Western blottings of fractionated proteins from rat WAT; Lane 3. water-soluble fraction; Lane 4 water-insoluble fraction. Proteins were separated in 10% SDS-PAGE and probed with following cellular protein marker antibodies: Anti-Na/K ATPase alpha1, a plasma membrane marker (Upstate, clone 464.6), anti-lamin B1, a nuclear envelope marker (ab16048, abcam Cambridge, MA), anti-ubiquinol-cytochrome C reductase core protein (abcam, ab 96333) and GAPDH, a cytosolic marker (Sigma). The specific protein bands were visualized by a substrate Opti-4CN (Bio-RAD). 

 

Kit includes:

Items

Quantity

Buffer A

15 ml

Buffer B

15 ml

1.5 ml Microfuge Tubes

20 units

Pestles for 1.5 ml Tubes

2 units

Filter Cartridge with Collection Tubes

20 units

Protein Extraction Powder

2 grams

 

  1. Markan, K. R., Naber, M. C., Small, S. M., Peltekian, L., Kessler, R. L., & Potthoff, M. J. (2017). FGF21 resistance is not mediated by downregulation of beta-klotho expression in white adipose tissue. Molecular Metabolism. http://dx.doi.org/10.1016/j.molmet.2017.03.009
  2. Liu, X., Tong, W., Zhao, X., Zhang, H., Tang, Y., & Deng, X. Chinese herb extract improves liver steatosis by promoting the expression of high molecular weight adiponectin in NAFLD rats. Molecular Medicine Reports.
  3. Subbaramaiah, K., Iyengar, N. M., Morrow, M., Elemento, O., Zhou, X. K., & Dannenberg, A. J. (2018). Prostaglandin E2down-regulates sirtuin 1 (SIRT1) leading to elevated levels of aromatase, providing insights into the obesity-breast cancer connection. Journal of Biological Chemistry, jbc-RA118.

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