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Cleaved caspase 8

Manufactured by Cell Signaling Technology
Sourced in United States, China

Cleaved caspase-8 is a laboratory product offered by Cell Signaling Technology. It is an antibody that detects the cleaved form of caspase-8 protein. Caspase-8 is a key enzyme involved in the initiation of apoptosis, or programmed cell death.

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209 protocols using cleaved caspase 8

1

Cytotoxic Effects of C086 on NSCLC

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The human NSCLC cell lines A549 and NCI-H1975 were obtained from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). The cells were cultured in RPMI-1640 media containing 10% fetal bovine serum, 100 U/mL penicillin, and 100 mg/mL streptomycin at 37°C in a humidified atmosphere of 5% CO2.
The bacterial strains and plasmids were obtained from the School of Life Science of Xiamen University, China. C086 (purity≥99%) was designed and synthesized by our laboratory (Figure 1B). C086 was dissolved in DMSO as a stock solution and diluted in culture media. Gefitinib was purchased from LC Laboratories (Woburn, MA, USA). Anti-Hsp90, anti-β-actin, anti-EGFR, anti-Ras, anti-C-Raf, anti-Akt, anti-P-Akt, anti-Mek, anti-P-Mek, anti-Erk½, anti-P-Erk, anti-C-Myc anti-Bax, anti-Bcl-2 (an apoptosis suppression protein), caspase-8, cleaved caspase-8, and the Apoptosis Antibody Sampler Kit containing PARP, cleaved PARP, caspase-9, cleaved caspase-9, caspase-3, cleaved caspase-3, caspase-7, cleaved caspase-7 were purchased from Cell Signaling Technology, Inc (Danvers, MA, USA). Annexin-V-APC/PI Apoptosis Detection Kit was purchased from Nanjing Keygen Biotech Co. Ltd (Nanjing, China). Propidium iodide (PI) was obtained from Sigma Aldrich.
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2

Comprehensive Protein Detection Techniques

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For immunoblotting and co-immunoprecipitation: Actin (Santa Cruz, ♯sc-47778; 1:5000), ATF6 (Cell Signaling Technology, ♯65880; 1:1000), BCL-2 (AbCam, ♯ab182858; 1:500), BCL-XL (Cell Signaling Technology, ♯2764; 1:1000), Cleaved-Caspase-8 (Cell Signaling Technology, ♯8592; 1:1000), Caspase-3 (Cell Signaling Technology, ♯9665; 1:1000), Caspase-9 (Cell Signaling Technology, ♯9508; 1:1000), CHOP (Cell Signaling Technology, ♯2895; 1:250), GFP (AbCam, ♯ab13970; 1:2000), GRP78 (Cell Signaling Technology, ♯3177; 1:1000), FLAG-HRP (Sigma Aldrich, ♯A8592; 1:4000), HA-HRP (Roche, ♯11867423001; 1:2000), IP3R1 (Thermo Fischer, ♯PA1-901; 1:1000), IP3R1 & IP3R2 [previously described77 ; 1:1000], IP3R3 (BD Biosciences, ♯610312; 1:1000), KDEL (AbCam, ♯ab12223; 1:2000), MCL-1 (Cell Signaling Technology, ♯5453; 1:1000), Nicastrin (BD Biosciences, ♯612290; 1:1000), PARP (Cell Signaling Technology, ♯9542; 1:1000), SERCA2 (Cell Signaling Technology, ♯4388; 1:1000), STIM1 (Cell Signaling Technology, ♯5668; 1:1000).
For immunofluorescence: DAPI (Thermo Fischer, ♯D1306; 1 µg/ml), HA (Cell Signaling Technology, ♯3724; 1:500), BAP31 (Enzo Life Sciences, ♯ALX-804-601-C100; 1:250).
For proximity ligation assay: HA (Cell Signaling Technology, ♯3724; 1:500), HA (Enzo Life Sciences, ♯ENZ-ABS118-0200; 1:200), IP3R1 (Thermo Fischer, ♯PA1-901; 1:200), IP3R3 (BD Biosciences, ♯610312; 1:200).
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3

Curcumin-induced Apoptosis in Cancer Cells

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Curcumin, CCK-8 kit, DMSO, and N-acetyl cysteine were purchased from Sigma Chemical Co (St. Louis, MO, United States) (Caspase-9, caspase-3,cleaved caspase-3,PARP,XIAP,p-Akt,Akt,GSK3,P-GSK3,FOXO1,P-FOXO1,GAPDH,cIap1,cIap2, Bcl-2, Bcl-xl, caspase 8, and cleaved caspase-8 antibodies were obtained from Cell Signaling Technologies (Beverly, MA, United States). Bax, p-H2AX, and cytochrome c antibodies and cisplatin were procured from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, United States). Annexin V fluorescein isothiocyanate (FITC), Propidium Iodide (PI), and p-H2AX (pS139) antibodies were purchased from BD Biosciences (San Jose, CA). z-VAD-FMK was obtained from Calbiochem (San Diego, CA, United States). CellROX Green was obtained from Invitrogen (MA, United States). Curcumin was dissolved in DMSO and further diluted in the cell culture media for the treatment of cells, so that the final concentration of DMSO in wells is 0.1% at the highest concentration of Curcumin used in the study. Viability assays showed that 0.1% DMSO is non-toxic to the cells (data not shown).
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4

Western Blot Analysis of Apoptosis Markers

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Western blotting was performed in accordance with a previously reported method 17. The assay was performed using antibodies against the following proteins: FADD, cleaved caspase 3, cleaved caspase 8, CHOP (Cell Signaling Technology, Danvers, MA, USA), DR5, DR4, Bip, β‐actin, Fas, Mcl‐1, Bcl‐2 and Bcl‐XL (BD Biosciences, San Jose, CA, USA).
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5

Protein Expression Analysis in Cardiac Tissue

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At the indicated time after reperfusion, whole LV tissues were collected and homogenized in lysis buffer containing 25 mM Hepes (pH 7.5), 1% Triton X100, 150 mM NaCl, 10% glycerol, 1 mM sodium orthovanadate, 50 mM NaF, 10 mM sodium pyrophosphate, and protease inhibitor cocktail (Sigma Chemical Co.). The total cell extracts were resolved by SDS-PAGE, and western blot analysis was performed as described previously [33 (link), 34 (link)]. Antibodies against tyrosine-phosphorylated STAT3 (pY-STAT3; #9145, D3A7, rabbit monoclonal, 1:200 dilution), serine-phosphorylated STAT3 (pS-STAT3; #9134, rabbit polyclonal, 1:200 dilution), STAT3 (#9132, rabbit polyclonal, 1:200 dilution), phosphorylated AKT (p-AKT; #4060, D9E, rabbit monoclonal, 1:200 dilution), AKT (#9272, rabbit polyclonal, 1:200 dilution), phosphorylated ERK1/2 (p-ERK1/2; #4370, D13.14.4E, rabbit monoclonal, 1:200 dilution), ERK1/2 (#9102, rabbit polyclonal, 1:200 dilution), cleaved caspase-3 (#9664, 5A1E, rabbit monoclonal, 1:200 dilution), cleaved caspase-8 (#8592, D5B2, rabbit monoclonal, 1:200 dilution), Bcl-xL (#2764, 54H6, rabbit monoclonal, 1:200 dilution), Bad (#9292, rabbit polyclonal, 1:200 dilution), Bax (#2772, rabbit polyclonal, 1:200 dilution), and Mcl-1 (#5453, D35A5, rabbit monoclonal, 1:200 dilution) were purchased from Cell Signaling Technology.
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6

Methamphetamine Cytotoxicity and Apoptosis

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Methamphetamine (METH) was purchased from the Ministry of Food and Drug Safety (Cheongju, Korea). Epicatechin (EC) was purified and received from Dr. Gil-Saeng Jeong, a professor of the College of Pharmacy, Keimyung University (Deagu, Korea). Methamphetamine (METH) was dissolved in dimethylsulfoxide (DMSO; Sigma, St. Louis, MO, USA) as a 1 M stock solution and stored at 4°C. Further dilution was done in cell culture medium. Antibodies against CHOP, BAX were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Antibodies against phospho-ERK, ERK, phospho-JNK, JNK, phospho-p38, p38, DR4, DR5, cleaved caspase-3, cleaved caspase-8, cleaved caspase-9, cleaved PARP, and β-actin were obtained from Cell Signaling Technology (Beverly, MA, USA). β-actin was used as a loading control.
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7

Western Blot Analysis of PCNA, SREBP1C, FASN

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Western blot analysis was performed as previously described [36 (link)]. Primary antibodies against PCNA and SREBP1C were from Santa Cruz Biotechnology, Santa Cruz, CA; antibodies against FASN were from BD Biosciences, Franklin Lakes, NJ; antibodies against cleaved-caspase 3, cleaved-caspase 8, cleaved-caspase 9, p-eIF2α, t-eIF2α and GCN2 were from Cell Signaling Technology, Beverly, MA.
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8

Western Blot Analysis of Cell Signaling

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Cells were lysed in radio-immunoprecipitation assay (RIPA) buffer (Sigma) and proteins were migrated on 10% or 12.5% SDS-PAGE gels and transferred to nitrocellulose or polyvinyldifluoride membranes. The membranes were blocked in 5% low fat milk for 1 h, and probed with the relevant primary antibodies overnight at 4 °C. The primary antibodies γ-H2AX, cleaved caspase-3, cleaved caspase-8, caspase-9, phospho-CHK1, phospho-CHK2, cyclin-D1, CDK6, CDK4, p21, ERK1/2, phospho-ERK1/2, p38 MAPK, phospho-p38 MAPK, JNK, phosphor-JNK, c-Jun, phospho-c-Jun and β-actin were obtained from Cell Signaling Technology (CST) (Beverly, MA, USA). Membranes were then probed with the appropriate secondary antibodies (CST) for 1 h at RT. The membranes were revealed using the Odyssey two-color infrared laser imaging system (LICOR, Lincoln, NE, USA). The ERK1/2 inhibitor U0126 and JNK inhibitor SP600125 were from Selleckchem.
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9

Apoptosis Signaling Pathway Profiling

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MDA-MB-231 cells were seeded at 106 cells/well in 6-well plates and allowed to attach overnight. Cells were then treated with fresh media containing LOE at 0.06 or 0.15 mg/ml for 3, 6, 12 and 24 h intervals. Treated cells were collected in RIPA buffer and sonicated to obtain lysates. Cell lysates were cleared of debris by centrifugation and protein concentration of lysates was estimated via the bicinchoninic acid (BCA) assay. Next, 20 µg of protein from each sample was subjected to SDS-polyacrylamide gel electrophoresis, transferred onto a polyvinyl difluoride (PVDF) membrane and immunoblotted. Primary antibodies for cyclin D1, cellular Inhibitor of Apoptosis Protein 2 (cIAP2), RIP1, cleaved caspase-8 and cleaved Poly-ADP Ribose Polymerase (PARP) were purchased from Cell Signaling Technologies, Danvers, MA, USA. Cleaved caspase-3 antibody was purchased from Epigenomics, WA. β-actin and β-tubulin antibodies were obtained from Sigma-Aldrich and Abcam, Cambridge, MA, USA, respectively. Quantification was carried out using ImageJ software (35 (link)).
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10

Tumor Cell Lysis and Western Blot Analysis

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Tumor cells were lysed on ice with ice-cold radioimmunoprecipitation (RIPA) buffer containing a protease inhibitor cocktail (Sigma-Aldrich) for 30 min. The tumor tissues in RIPA buffer were treated by ultrasound. Then, soluble protein concentrations in lysate were determined by using a BCA protein assay kit (Thermo Scientific, Fremont, CA, USA). Western blot analysis was performed mainly as previously described [21 (link)]. The following antibodies were used: caspase-3, cleaved caspase-3, caspase-8, cleaved caspase-8 (9662S, 9661S, 4790S, 9496S respectively, Cell Signaling Technology, Danvers, MA, USA), RIP1 (610,458, BD Biosciences), pRIP1 (65746S, Cell Signaling Technology, Danvers, MA, USA), RIP3 (13,526, Cell Signaling Technology, Danvers, MA, USA), pRIP3 (ab209384, Abcam, Cambridge, UK), MLKL (ab184718, Abcam, Cambridge, UK), pMLKL (ab187091, Abcam, Cambridge, UK), JNK (9252, Cell Signaling Technology, Danvers, MA, USA), pJNK (4668, Cell Signaling Technology, Danvers, MA, USA), GAPDH (5174S, Cell Signaling Technology, Danvers, MA, USA) and corresponding secondary antibodies (Jackson ImmunoResearch, PA, USA).
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