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Muse annexin dead cell kit

Manufactured by Merck Group
Sourced in United States

The Muse Annexin & Dead Cell kit is a flow cytometry-based assay that quantifies the percentage of viable, early apoptotic, late apoptotic, and dead cells within a sample. The kit utilizes Annexin V to detect phosphatidylserine exposure and a dead cell marker to identify non-viable cells.

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4 protocols using muse annexin dead cell kit

1

Autophagy Regulation in Breast Cancer Cells

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Human MDA-MB-231 and MCF-7 cells were purchased from American Type Culture Collection (ATCC) (Manassas, VA). Leibovitz’s L-15 medium, RPMI-1640 medium, Fetal Bovine Serum (FBS), Penicillin-streptomycin Cocktails and Cystatin C (Catalog number: PHP0044) were obtained from Thermo Scientific (Rockford, IL). SAHA was purchased from Sigma-Aldrich (St. Louis, MO). Muse Cell Cycle kit, Muse Annexin & Dead Cell kit, and Muse Count & Viability kit were from Millipore (Darmstadt, Germany). Human MAPK Antibody Array kit was purchased from R&D Systems (Minneapolis, MN). High Pure RNA Isolation kit and Transcriptor First Strand cDNA Synthesis kit were obtained from Roche Diagnostics GmbH (Mannheim, Germany). Exprofile Human autophagy Gene qPCR Array kit was obtained from Genecopoeia (Rockville, MD). Power SYBR Green PCR Master mix, RIPA Cell Lysis buffer and BCA Protein Assay kit were from Life Technologies (Austin, TX). Polyclonal anti-beclin-1 antibody, polyclonal anti-Atg3 antibody, polyclonal anti-Atg5 antibody, polyclonal anti-Atg7 antibody, polyclonal anti-Atg12 antibody, polyclonal anti-Atg16 antibody, polyclonal anti-Atg4A antibody, polyclonal anti-Atg4B antibody, polyclonal anti-Atg9B antibody, polyclonal anti-LC3II antibody were obtained from Abcam Inc (Cambridge, MA). Protease inhibitor and other chemicals were purchased from Sigma-Aldrich (St. Louis, MO).
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2

Apoptosis Evaluation in Breast Cancer Cells

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Human MDA-MB-231 and MCF-7 cells were purchased from American Type Culture Collection (ATCC) (Manassas, VA). Leibovitz’s L-15 medium, RPMI-1640 medium, Fetal Bovine Serum (FBS) and Penicillin-streptomycin Cocktails were obtained from Thermo Scientific (Rockford, IL). Suberanilohydroxamic acid (SAHA) was purchased from Sigma-Aldrich (St. Louis, MO). Recombinant human TRAIL/Apo2 Ligand was from Peprotech (Rocky Hill, NJ). Muse Cell Cycle kit, Muse Annexin & Dead Cell kit, and Muse Count & Viability kit were from Millipore (Darmstadt, Germany). Human Apoptosis Antibody Array kit was purchased from R&D Systems (Minneapolis, MN). High Pure RNA Isolation kit, Annexin-V-FLUOS staining kit and Transcriptor First Strand cDNA Synthesis kit were obtained from Roche Diagnostics GmbH (Mannheim, Germany). Exprofile Human Cell Cycle Tox and Cancer Related Gene qPCR Array kit and Exprofile Human EGF/PDGF Signaling Related Gene qPCR Array kit were obtained from Genecopoeia (Rockville, MD). Power SYBR Green PCR Master mix, Calcein-AM dye, RIPA Cell Lysis buffer and BCA Protein Assay kit were from Life Technologies (Austin, TX). CellTiter 96AQueous One Solution Cell Proliferation Assay kit was obtained from Promega (Madison, WI). Protease inhibitor and other chemicals were purchased from Sigma-Aldrich (St. Louis, MO).
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3

Cordycepin's Anti-inflammatory Effects

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Fetal bovine serum (FBS), 1% (w/v) penicillin-streptomycin and phosphate-buffered saline (PBS) were obtained from Thermo (Paisley, Scotland, UK). Dulbecco’s Modified Eagle’s Medium (DMEM) was purchased from Sigma-Aldrich (St Louis, MO, USA). Cordycepin (3′-Deoxyadenosine, from Cordyceps militaris), Pyrrolidine dithiocarbamate (PDTC), and SP600125 were purchased from Sigma-Aldrich. TNF-α was purchased from R & D system (R&D Systems, Minneapolis, MN, USA). A Muse Annexin & Dead Cell kit was from Millipore (Millipore, Billerica, MA, USA). Whole cell lysis buffer was purchased from Intron (Seoul, Korea), and transfection reagent Hilymax and CCK-8 were from Dojindo (Dojindo, Japan). Antibodies against CCL5, NF-κB, p-IκB, IκB, p65, p-Akt, Akt, caspase-3, and β-actin were purchased from Cell Signaling (Beverly, MA, USA). Antibodies against PARP-1 and Bax were from Santa Cruz Biotechnology (Dallas, TX, USA).
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4

Bioflavonoids' Effects on Pharynx Cancer Cells

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Human Detroit 562 cells were purchased from the European Collection of Authenticated Cell Cultures (catalogue no. 87042205, European Collection of Authenticated Cell Cultures, Porton Down, Salisbury, England). Eagle's minimum essential medium (EMEM), fetal bovine serum (FBS) and penicillin-streptomycin cocktails were purchased from Thermo Scientific (Rockford, IL, USA). Bioflavonoids compounds rutin (Rut), quercetin (Que) and hesperidin (Hes) were obtained from Sigma-Aldrich (St. Louis, MO, USA) and the Muse Annexin & Dead Cell kit and the Muse Count and Viability kit is manufactured by Millipore (Darmstadt, Germany).
Pharynx cancer cell line Detroit 562 was grown according to the manufacturer's specification using EMEM supplemented with 10% FBS. The cells were cultured in bottles of 75 cm 2 (PAA) with the addition of antibiotics: 100 IU/mL penicillin, 100 µL/mL streptomycin and 0.25 µL/mL amphotericin B. Cells were cultured in a CO 2 incubator at 37 • C and in a saturated steam atmosphere with 5% carbon dioxide (CO 2 ).
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