Adipose Tissue Nuclear Isolation

Revision as of 20:41, 27 March 2017 by Davebridges (Talk | contribs) (copied initial protocol from Kang)

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Revision as of 20:41, 27 March 2017 by Davebridges (Talk | contribs) (copied initial protocol from Kang)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

From Kang et al

Epididymal adipose tissue was collected from chow- (n=15) and high-fat-fed (n=7) C57BL/6 mice. Pooled fat pads were minced and dounce homogenized with 10 strokes in hypotonic lysis buffer (10mM HEPES, pH 7.5, 10mM KCl, 1.5mM MgCl2 , 250mM sucrose, 0.5% NP40, and protease inhibitor cocktail). Lysates were filtered through a 100 µm cell strainer and spun at 1, 500g for 5 min. Lipid and cytoplasmic fractions were removed and the nuclear pellet was resuspended in lysis buffer

References

Kang S, Tsai LT, Zhou Y, Evertts A, Xu S, Griffin MJ, Issner R, Whitton HJ, Garcia BA, Epstein CB, Mikkelsen TS, Rosen ED. Identification of nuclear hormone receptor pathways causing insulin resistance by transcriptional and epigenomic analysis. Nat Cell Biol. 2015; 17: 44–56. doi: 10.1038/ncb3080.