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Caspase activity assay kits

Manufactured by R&D Systems
Sourced in United States

The Caspase activity assay kits are laboratory tools used to measure the activity of caspase enzymes, which play a key role in the process of apoptosis or programmed cell death. The kits provide a standardized and quantitative method to detect and analyze caspase activity in various experimental systems.

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6 protocols using caspase activity assay kits

1

Anticancer Activity of Vitis coignetiae Pulliat

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Human lung cancer cell lines A549 cells from the American type culture collection (Rockville, MD, USA) were cultured in RPMI 1640 medium (Invitrogen Corp, Carlsbad, CA, USA) supplemented with 10% (v/v) fetal bovine serum (FBS) (GIBCO BRL, Grand Island, NY, USA), 1 mM L-glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin at 37°C in a humidified atmosphere of 95% air and 5% CO2. Caspase activity assay kits were obtained from R and D Systems (Minneapolis, MN, USA). Antibodies against cyclin D1, c-Myc, MMP-2, ICAM-1, and VEGF were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Antibody against β-actin was from Sigma (Beverly, MA). Peroxidase-labeled donkey anti-rabbit and sheep anti-mouse immunoglobulin, and an enhanced chemiluminescence (ECL) kit were purchased from Amersham (Arlington Heights, IL). All other chemicals not specifically cited here were purchased from Sigma Chemical Co. (St. Louis, MO). The anthocyanins were isolated from Vitis coignetiae Pulliat.
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2

Culturing MKN28 Gastric Carcinoma Cells

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The MKN28 human gastric carcinoma cells obtained from the American type culture collection (Manassas, VA, USA) were cultured in RPMI medium (Invitrogen Corp, Carlsbad, CA, USA) supplemented with 10% (v/v) fetal bovine serum (FBS) (GIBCO BRL, Grand Island, NY, USA), 1 mM L-glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin at 37 °C in a humidified atmosphere of 95% air and 5% CO2. Antibodies against TRAIL, DR4, DR5, Fas, FasL, XIAP, a cellular inhibitor of apoptosis protein-1 (cIAP-1), cIAP-2, caspase-3, -8, -9, Bcl-2, Bax, FlipL, FlipS, PARP, β-catenin, and PLCγ1 were purchased from Santa Cruz Biotechnology (Dallas, Texas, USA). An antibody against β-actin was from Sigma (Beverly, MA, USA). Caspase activity assay kits were obtained from R&D Systems (Minneapolis, MN, USA). An enhanced chemiluminescence (ECL) kit was purchased from Amersham (Arlington Heights, IL, USA). 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolylcarbocyanine iodide (JC-1) were obtained from Calbiochem (San Diego, CA, USA). All other chemicals not specifically cited here were purchased from Sigma–Aldrich (St. Louis, MO, USA). All these solutions were stored at −20 °C. Stock solutions of 4,6-diamidino-2-phenylindole (DAPI, 100 μg/mL) and propidium iodide (PI, 1 mg/mL) were prepared in phosphate-buffered saline (PBS).
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3

Cell Death Mechanisms Evaluation

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TSA and recombinant human TRAIL were purchased from Calbiochem (San Diego, CA, USA) and KOMA Biotech Inc. (Seoul, Republic of Korea), dissolved in dimethyl sulfoxide (DMSO, Sigma-Aldrich Chemicals, St. Louis, MO, USA), and then diluted with the medium to the desired concentration prior to use. Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS), glutamine, penicillin, and streptomycin were purchased from GIBCO-BRL (Gaithersburg, MD). 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphnyl-2H-tetrazolium bromide (MTT), 4,6-diamidino-2-phenylindole (DAPI), and propidium iodide (PI) were obtained from Sigma-Aldrich. Annexin V-fluorescein isothiocyanate (FITC) was obtained from Calbiochem. 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimid azolylcarbocyanine iodide (JC-1) and caspase activity assay kits were purchased from R&D Systems (Minneapolis, MN, USA). Antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA), Chemicon (Temecula, CA, USA), PharMingen (San Diego, CA, USA) and Sigma-Aldrich. Peroxidase-labelled donkey antirabbit, sheep antimouse immunoglobulin, and enhanced chemiluminescence (ECL) kits were purchased from Amersham (Arlington Heights, IL, USA). All other chemicals were purchased from Sigma-Aldrich.
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4

Caspase Activity Assay Protocol

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The activity of caspases was determined using Caspase Activity Assay Kits (R&D Systems, Minneapolis, MN, USA), according to the protocol of the manufacturer. Briefly, the detached cells and adherent cells were harvested, washed with PBS, and cell pellets resuspended in the lysis buffer provided in the kit. The supernatants were collected and incubated with the supplied reaction buffer containing dithiothreitol, with or without tetrapeptides labeled with p-nitroaniline (pNA) at 37 °C for 2 h under light-shielded conditions. The caspase activities were determined by measuring changes in absorbance at 405 nm using a microplate reader.
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5

Caspase Activity Assay Protocol

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The activity of caspases was measured using caspase activity assay kits (R&D Systems, Minneapolis, MN, USA), according to the manufacturer's protocol. In brief, cells were harvested, and lysed in the lysis buffer provided in the kit. The supernatants were collected, incubated with the supplied reaction buffer containing dithiothreitol, with or without substrates [Asp-Glu-Val-Asp (DEAD) for caspase-3; Ile-Glu-Thr-Asp (IETD) for caspase-8; and Leu-Glu-His-Asp (LEHD) for caspase-9] labeled with p-nitroaniline (pNA) at 37°C for 2 h in the dark. The optical density of the reaction mixture was determined by absorbance at 405 nm using a microplate reader.
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6

Apoptosis Regulation in U937 Cells

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U937 human leukemic cells from the American type culture collection (Rockville, MD, USA) were cultured in RPMI 1640 medium (Invitrogen Corp, Carlsbad, CA, USA) supplemented with 10% (v/v) fetal bovine serum (FBS) (GIBCO BRL, Grand Island, NY, USA), 1 mM L-glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin at 37℃ in a humidified atmosphere of 95% air and 5% CO2. Antibodies against Bcl-2, Bid, inhibitors of apoptosis protein-1 (IAP-1), IAP-2, X-linked IAP (XIAP), pro-caspase 3, pro-caspase 8, and pro-caspase 9 were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Antibody against poly (ADP-ribose) polymerase (PARP) was purchased from PharMingen (San Diego, CA, USA). Antibody against β-actin was from Sigma (Beverly, MA). Peroxidase-labeled donkey anti-rabbit and sheep anti-mouse immunoglobulin, and an enhanced chemiluminescence (ECL) kit were purchased from Amersham (Arlington Heights, IL). Caspase activity assay kits were purchased from R&D systems (Minneapolis, MN, USA). All other chemicals not specifically cited here were purchased from Sigma Chemical Co. (St. Louis, MO, USA).
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