or 412% precast Bis-Tris gel. Proteins were transferred from the gel to a nitrocellulose membrane using the iBlot Dry Blotting System. Specific proteins were Neuromedin N custom synthesis detected by immunoblotting using primary antibodies anti-PHB1, anti-PHB2, anti-C/EBPb, anti-PPARc, anti-aP2, anti-HSP90 anti-b-actin, anti-ERK, anti-p-ERK and anti-porin. Horseradish peroxidase -conjugated anti-rabbit IgG and anti-mouse IgG were used as secondary antibodies in a 6-well plate. 3T3-L1 cells were seeded and treated with differentiation medium in the plate as described above. The cells were then fixed with 4% paraformaldehyde in PBS for 30 min, Prohibitins Are Required for Adipogenesis followed by PBS wash and subsequent treatment with cold absolute methanol for 5 min at 220uC. The cells were rinsed with PBS and permeabilized with 0.2% Triton X-100 in PBS for 10 min. After blocking with 5% BSA in PBS for 1 hour, the cover glasses were incubated with anti-PHB1, antiPHB2 or anti-Cytochrome C antibody in 0.1% BSA in PBS at room temperature for two hours. The cells were then washed with PBS and incubated with Rhodamine or Alexa Fluor 488 conjugated secondary antibody in 0.1% BSA in PBS at room temperature for 1 hour. Thereafter, the cover glasses were mounted upside down on microscope slides containing mounting medium. The mounted slides were examined under an Olympus BX41 microscope equipped with an Optronics Magnafire digital camera and Prior Proscan motorized driven stage. For each image, specific antibody 15256538” staining was merged with CytC using Soft Imaging System software that results in virtually no pixel shifting during the image merge. Representative photomicrographs were arranged using Adobe Photoshop without any further adjustment to maintain the true 
nature of the findings. systems; Bannockburn, IL) equipped with a 636/1.40 NA oilimmersion objective lens was used to characterize the optical properties of these samples. Images were captured with a scanning speed of 400 Hz and image resolution of 5126512 pixels, and then analyzed using Leica Application Suite, Advanced Fluorescence software. Measurement of ATP concentration The adenosine triphosphate concentration was measured with an ENLITEN ATP assay system bioluminescence detection kit. Briefly, three days after transfection of 3T3-L1 cells in a 96-well plate with siRNA oligonucleotides, 0.5% trichloroacetic acid was added for ATP efficient release. Then, 25 mmol/L Tris-acetate was used for neutralization. After addition of recombinant Luciferase/Luciferin reagent, luminescence was measured using a 10-second integration time with a microplate luminometer and SOFTmax PRO software, and was normalized to protein concentration. The ATP standard curve was generated by using the ATP standard included in the kit. Isolation of mitochondria Isolation of mitochondria was performed using a mitochondria isolation kit according to the manufacturer’s protocol and previous descriptions. Briefly, pre- and seven days post-adipocyte differentiation 3T3-L1 cells in 100 mm dishes were harvested using trypsinization. A reagent-based method was used for ” cell homogenization allowing multiple samples to be processed concurrently. To obtain a more purified fraction of mitochondria with more than 50% reduction of lysosomal and peroxisomal contaminants, the last step for pelleting mitochondria was performed using centrifugation for 15 minutes at 3,0006 g rather than at standard 12,0006 g. Reactive oxygen species detection ROS were detected
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