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Anti c ebp homologous protein chop

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Anti-C/EBP-homologous protein (CHOP) is a laboratory product used for research purposes. CHOP is a transcription factor that plays a role in the cellular response to endoplasmic reticulum stress. This product can be used to study CHOP and its functions in various experimental systems.

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3 protocols using anti c ebp homologous protein chop

1

Endoplasmic Reticulum Stress Protein Analysis

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Nitrocellulose paper (#1620177), Laemmle sample buffer (#1610737) and HRP substrate (IMMUN-STAR #1705040) were from Bio-Rad (Hercules, CA, USA). The Bicinchonic Acid Protein Assay Kit (#BCA1; B9643) and protein inhibitor cocktail (#P2714) were from Sigma Chemical Co. (St. Louis, MO). The anti-heat shock protein 70 (HSP-70) (rabbit polyclonal, SC-71060R), anti-C/EBP-homologous protein (CHOP) (rabbit polyclonal, SC-575) and anti-X-box binding protein 1 (XBP-1) (M186) (rabbit polyclonal, SC-7176) antibodies were from Santa Cruz Biotechnology, Inc. (Dallas, Texas, USA). The anti-glucose regulating protein 78 (BIP) (rabbit polyclonal, #C50B12) antibody was from Cell Signaling Technology (Beverly, MA, USA). Routine reagents were purchased from Sigma Chemical Co. (St. Louis, MO, USA).
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2

Western Blot Analysis of Kidney Protein Markers

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Equal amounts of protein samples from mouse kidney were separated by SDS-PAGE, transferred onto polyvinylidene fluoride membranes by electroblotting and incubated at 4 °C overnight with primary antibodies (anti-PGC-1α (Abcam, Cambridge, UK), anti-ATF6 (Santa Cruz Biotechnology, USA), anti-C/EBP homologous protein (CHOP, Santa Cruz Biotechnology, USA), anti- phospho-IRE1α (p- IRE1α, Invitrogen, USA), anti-phospho-PERK (p-PERK, Invitrogen, USA), anti-cleaved Poly (ADP-ribose) polymerase 1 (c-PARP1, Santa Cruz Biotechnology, USA), anti-mitofusin 2 (Mfn2, Abcam, Cambridge, UK), anti-apoptotic protein B-cell lymphoma 2 (Bcl2, Santa Cruz Biotechnology, USA), anti-Bcl2-associated X protein (Bax, Santa Cruz Biotechnology, USA), anti-cleaved caspase 3 (Cell Signaling Technology, USA), anti-caspase 12 (Cell Signaling Technology, USA), anti-Notch1 (Abcam, Cambridge, UK), anti-Hes1(Abcam, Cambridge, UK) and anti-GAPDH (Invitrogen, USA)). Next, the membranes were incubated with horseradish peroxidase–conjugated goat anti–rabbit secondary antibody (Invitrogen, USA) at 25 °C for 1.5 h. The chemiluminescent bands were visualized using a chemiluminescence detection system and quantified using ImageJ software.
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3

Comprehensive Antibody Staining Protocol

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The following antibodies were used in this study: anti-FLAG (M2, Sigma Aldrich, St. Louis, MO), anti-HA (H6908, Sigma;3F10, Roche, Mannheim, Germany), anti-SOD1 (SOD100, Enzo Life Science, Farmingdale, NY; C17, Santa Cruz Biotechnology, Santa Cruz, CA), anti-chromogranin B (26102, QED Bioscience, San Diego, CA; PA1-10839, Thermo, Rockford, IL), B8H10 (33), C4F6 (37), anti-TGN38 (M290, Santa Cruz), anti-synaptophysin (D35E4, Cell signaling technology, Danvers, MA), anti- synaptotagmin V (46, Santa Cruz), anti-Akt1 (B1, Santa Cruz), anti-Mac2 (hybridoma from ATCC, Rockville, MD, USA), anti-glial fibrillary acidic protein (GFAP) (GA5, Cell signaling), anti-choline acetyltransferase (ChAT) (AB144P, Millipore, Billerica, MA), anti-neuronal nuclear antigen (NeuN) (MAB5294, Millipore), anti-actin (Millipore), anti-human protein gene product 9.5 (PGP9.5) (7863-0504, AbD Serotec, Raleigh, NC), anti-vesicular acetylcholine transport (VAChT) (Milipore), rhodamine conjugated α-Bungarotoxin (Invitrogen, Carlsbad, CA), anti-Bip (3177, Cell Signaling; ab21685, abcam, Cambridge, MA), anti-phospho-protein kinase-like endoplasmic reticulum kinase (PERK) (16F8, Cell Signaling), anti-C/EBP-homologous protein (CHOP) (F168, Santa Cruz), anti-caspase 12 (2202, Cell Signaling), SMI32 (Covance, Princeton, NJ), anti-SRY (E19, Santa Cruz).
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