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4 protocols using phosstop protease inhibitor cocktail

1

Western Blot Analysis of Cardiac Protein Markers

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Left ventricular tissue was obtained 24 h or 5 d after multiple trauma or sham procedure and homogenized and lysed using RIPA Lysis Buffer (EMD Millipore, Darmstadt, Germany) containing complete Mini-protease inhibitor and PhosSTOP protease inhibitor cocktail (Roche). Protein concentrations were determined in homogenates using the Pierce® BCA Protein Assay Kit (Thermo Fischer Scientific, Waltham, MA, USA). Samples were loaded under reducing conditions onto a Mini-Protean®TGX™ Precast Gel (Bio-Rad Laboratories, Munich, Germany). After electrophoresis, the proteins were transferred by a Trans-Blot Turbo Transfer System using Mini Transfer Packs (Bio-Rad). The blots were blocked with 5% milk (C5aR1) or 5% bovine serum albumin (connexin 43 (Cx43)) in tris-buffered saline for 1 h at room temperature (RT) and incubated with antibodies (see below) overnight at 4°C. For analysis of the rat heart homogenates, rabbit anti-C5aR1 (Proteintech, Manchester, UK) and for Cx43 rabbit anti-connexin (Cell Signaling Technology, Danvers, MA) were used. HRP-conjugated anti-rabbit immunoglobulin G (IgG) (Cell Signaling) was used as a secondary antibody. Chemiluminescent HRP Hy Glo™ (Denville Scientific Inc, South Plainfield, NJ) was used. The blots were analyzed by ChemiDoc (BioRad Laboratories GmbH, Munich, Germany) and Image Lab Software (Version 5.2, BioRad).
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2

Western Blot Analysis of Cardiac Proteins

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Left ventricular tissue was obtained 72 h after multiple trauma or sham procedure and homogenized and lysed by using 1x RIPA Lysis Buffer (EMD Millipore) containing complete Mini-protease inhibitor and PhosSTOP protease inhibitor cocktail (Roche). Protein concentrations were determined in homogenates using Pierce® BCA Protein Assay Kit (Thermo Scientific). The samples were loaded under reducing conditions onto a 4–20% Mini-Protean®TGX™ Precast Gels (Bio-Rad Laboratories). After electrophoresis proteins were transferred by a Trans-Blot Turbo Transfer System using Mini Transfer Packs (both from Bio-Rad). The blots were blocked with 5% milk in tris-buffered saline (TBS) for 1 hour at room temperature (RT) and then incubated with antibodies (see below) overnight at 4 °C. For analysis of the pig heart homogenates rabbit anti-C5aR1 (Proteintech Group, Rosemont, IL, USA) and rabbit anti-Cx43 (Cell Signalling, Danvers, MA, USA) were used. After washing, HRP-anti-rabbit (Cell Signaling Technology, Danvers, MA, USA) was used as secondary antibody (1:15,000) at RT for 1 h followed by an additional washing step. Chemiluminescent HRP Hy Glo™ (Denville Scientific Inc, South Plainfield, NJ) was used for developing. The blots were analyzed by the ChemiDoc (BioRad Laboratories GmbH, Munich, Germany) and the Image Lab Software (Version 5.2, BioRad).
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3

CLP-Induced Changes in Mouse Cardiac Proteins

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Mouse hearts were obtained 8, 12, 16, 24 and 48 hour after CLP and homogenized and lysed by using 1x RIPA Lysis Buffer (EMD Millipore) containing complete Mini-protease inhibitor and PhosSTOP protease inhibitor cocktail (Roche). Protein concentrations were determined in homogenates using Pierce® BCA Protein Assay Kit (Thermo Scientific). After centrifugation, pellets were resuspended in Laemmli Sample Buffer (Bio-Rad Laboratories) and boiled. After a last centrifugation step the samples were loaded under reducing conditions onto a 7.5% (NCX-1 and SERCA2) Mini-Protean®TGX™ Precast Gels (Bio-Rad Laboratories). After electrophoresis proteins were transferred by a Trans-Blot Turbo Transfer System using Mini Transfer Packs (both from Bio-Rad). The blots were blocked with 5% milk in TBS for 1 hour at RT and then incubated with antibodies (see below) overnight at 4°C. For analysis of the mouse heart homogenates, anti-SERCA2 ATPase (Abcam) and mouse anti-Na+-Ca2+-Exchanger (NaCX-1, EMD Millipore) were used. After washing, HRP-conjugated anti-mouse or anti-rabbit antibody (GE Healthcare, Buckinghamshire, UK) was used as secondary antibody (1:10,000) at RT for 1 hr followed by an additional washing step. Chemiluminescent HRP Hy Glo™ (Denville Scientific Inc, South Plainfield, NJ) was used for developing.
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4

Tissue Homogenization and Protein Extraction

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Frozen tissue samples were homogenised in RIPA (Radio-ImmunoPrecipitation Assay) lysis buffer (50mM Tris pH 7.5, 150mM sodium chloride, 1% NP-40, 0.1% SDS, 0.5% sodium deoxycholate, 1 x Complete protease inhibitor cocktail (Roche), 1 x PhosSTOP protease inhibitor cocktail (Roche)) at ∼200 mg/ml using a Polytron homogeniser at room temperature. Homogenates were immediately cleared by centrifugation at 16 000 g for 15 min at 4°C. Protein concentration was determined using the Pierce™ BCA assay kit (ThermoFisher Scientific, Loughborough, UK). The supernatants were adjusted by addition of further RIPA buffer to make each sample 175 l at 2 mg/ml.
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