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Live dead viability cytotoxicity kit

Manufactured by Promega
Sourced in United States

The LIVE/DEAD Viability/Cytotoxicity kit is a fluorescence-based assay that can be used to determine the viability of cells. The kit utilizes two fluorescent dyes: one that labels live cells and another that labels dead cells. This allows for the simultaneous detection and quantification of live and dead cells within a sample.

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3 protocols using live dead viability cytotoxicity kit

1

Peptide-Mediated Myoblast Proliferation

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Two tetrameric self-assembling peptides CH-01 and CH-02 were custom-synthesized in our Laboratory for Nanomedicine. Mouse myoblast cells (C2C12) were obtained from ATCC, USA. The following materials were ordered from Gibco, USA: Dulbecco’s modified eagle medium (DMEM), fetal bovine serum (FBS), heat-inactivated horse serum, Dulbecco’s phosphate-buffered saline (PBS) solution, and penicillin-streptomycin (P/S) antibiotics. An 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell proliferation assay kit and a LIVE/DEAD Viability/Cytotoxicity kit were purchased from Promega, USA. Immunostaining antibody myosin heavy chain (MHC) was purchased from Abcam. Cell culture flasks and 96-well plates were ordered from Corning, USA.
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2

Synthesis and Culturing of Peptides and Halophilic Archaea

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The self-assembling peptide IK6 (Ac-ILVAGK-NH2) was custom synthesized by Bachem AG (Budendorf, Switzerland). Human embryonic kidney cells (HEK293) were purchased from American Type Culture Collection (ATCC; USA). Cells were cultured in medium Dulbecco’s modified Eagle’s medium-high glucose (DMEM-HG; Gibco Thermo Fisher Scientific, USA). T175 or T75 cell culture flasks and 96- and 48-well plates were purchased from Corning, USA. Halobacterium sp. NRC-1 was obtained from Carolina Biological Supply (Burlington, NC, USA) and cultured in CM+ medium containing 4.3M NaCl and trace metals at 42°C with shaking as previously described[45 ]. H. volcanii H1895 and its corresponding vector pTA963 were kindly provided by Dr. Thorsten Allers (Institute of Genetics, School of Biology, University of Nottingham, Queen’s Medical Centre, Nottingham, UK). H. volcanii and derivatives were cultured in the Hv-YPC medium at 45°C with shaking as previously described[46 (link),47 (link)]. For solid media, 2% (w/v) agar was added. The CellTiter-Glo® luminescent 3D cell viability assay kit, LIVE/DEAD® Viability/Cytotoxicity kit and Actin Cytoskeleton/Focal Adhesion Staining kit were purchased from Promega, USA, Life Technologies™, USA, and Sigma-Aldrich, USA, respectively.
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3

Doxorubicin Nanoparticle Cytotoxicity Assay

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Doxorubicin hydrochloride (DOX) was purchased from Sangon (Shanghai, China). Calcium chloride (CaCl 2 , 96%), disodium hydrogen phosphate (Na 2 HPO 4 , 99%) were obtained from Titan (Shanghai, China). Dopamine hydrochloride and 2-Amino-2-(hydroxymethyl)-1,3-propanediol (Tris) were obtained from Biofroxx (Guangzhou, China). FITC was purchased from Yeasen (Shanghai, China). Bovine serum albumin (BSA), 4′,6-diamidino-2-phenylindole (DAPI), 70 µm cell screen mesh, Live/Dead Viability/Cytotoxicity Kit (Promega), Advanced DMEM/F12 (Gibco), B-27 Supplement(50X), N2-supplement (100X), N-acetyl-L-cysteine, Recombinant Mouse EGF were purchased from Gibco (USA). Puromycin, Zeocin, Plasmocin, trypsin-ethylenediaminetetraacetic acid (trypsin-EDTA) were gained from Invitrogen (USA). Matrigel Matrix was obtained from Corning (USA). CS10 was obtained from Stem Cell (Canada). CellTiter-Glo 3D Cell Viability Assay was purchased from Promega (USA). Rhodamine-phalloidin was purchased from Thermo Fisher (USA).
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