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Image Search Results
Journal: Autophagy
Article Title: Mutant HTT (huntingtin) impairs mitophagy in a cellular model of Huntington disease
doi: 10.1080/15548627.2020.1728096
Figure Lengend Snippet: PolyQ tract in mutant HTT does not affect the polyUB labeling of mitochondria. (a) Representative immunoblots of total polyUB (total-UB) and phosphorylated ubiquitin (Ser65; p-UB-S65) in total homogenate and isolated mitochondria from ST-Q7 and ST-Q111 control cells (vehicle, CTR) or treated with rotenone (Rot, 1 μM, 4 h) or CCCP (10 μM, 24 h). Protein levels were normalized relative to Ponceau staining and quantification is depicted as fold-change to control ST-Q7 cells of at least three independent experiments. (b) Representative immunoblots of BNIP3 and BNIP3L in isolated mitochondria from ST-Q7 and ST-Q111 control cells (vehicle, CTR) or treated with rotenone (Rot, 1 μM, 4 h) or CCCP (10 μM, 24 h). Protein levels were quantified using all bands present in each lane independently of the molecular weight or oligomerization state (indicated with line and arrows) and were normalized relative to Ponceau staining and quantification is depicted as fold-change to control ST-Q7 cells. Data are presented as mean ± s.e.m of at least 3 independent experiments and no significant changes were observed after statistical analysis
Article Snippet: OPTN (10837-1-AP) from Proteintech Group, HTT (MAB2166) from Chemicon, SQSTM1/p62 (GP62-C) and NBR1 (H00004077-M01) from Abnova, anti-DNA (AC-30-10) from Progen, MTOR (GT649) mouse (GTX630198) from Genetex, total-UB (U5379) and ACTB/β-actin (A5441) from Sigma-Aldrich, BNIP3 (M01469),
Techniques: Mutagenesis, Labeling, Western Blot, Ubiquitin Proteomics, Isolation, Control, Staining, Molecular Weight