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Bio tek elx800 universal microplate reader

Manufactured by Agilent Technologies
Sourced in United States

The BIO-TEK ELx800 Universal Microplate Reader is a compact and versatile laboratory instrument designed for absorbance-based microplate-based assays. It features a high-performance monochromator-based optical system and supports a wide range of microplate formats, enabling accurate and reliable measurements across various applications.

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4 protocols using bio tek elx800 universal microplate reader

1

Cytotoxicity Evaluation of Nanoparticles

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The cytotoxic effect of the nanoparticles against the cells was measured using the Cell Counting Kit-8 (Dojindo Laboratories, Kumamoto, Japan) according to the manufacturer’s protocols. Briefly, cells were seeded in 96-well plates with a density of 5×103 cells per well overnight. The cells were incubated with a series of concentrations of the nanoparticles or free salinomycin. After 48 hours or 72 hours, the cell proliferation was evaluated by adding 10 μL Cell Counting Kit-8 solution to each well of the plate. Two hours after incubation, the absorbance was measured at 450 nm/630 nm with the BIO-TEK ELx800 Universal Microplate Reader (BioTek, Winooski, VT, USA). The cell viability was calculated using the following formula:
([AEAB]/[AEAB])×100% where AE, AC, and AB are defined as the absorbance of experimental samples, untreated samples, and blank controls, respectively.
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2

Propranolol Cytotoxicity on Hemangioma Stem Cells

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The cytotoxic effect of propranolol against the HemSCs was measured using a Cell Counting Kit-8 kit (CCK-8 kit; Dojindo laboratories, Kumamoto, Japan). Briefly, HemSCs (10,000 per well) were seeded at subconfluency on a fibronectin-coated 24-well plate in EGM-2 with 20% FBS. Four hours later, the media was removed and the cells treated with various concentrations of propranolol, PL, and PLIM. After a period of time, the cell viability was determined using the CCK-8 kit. Briefly, the cell viability was evaluated by adding CCK-8 (10 μL) solution to each well of the plate. After incubation for 2 h, the absorbance was measured at 450 nm/630 nm using a BIO-TEK ELx800 Universal Microplate Reader (Bio-Tek, Winooski, VT, USA). The cell viability was calculated using the formula: (AE − AB)/(AC − AB) ×100%. AE, AC, and AB are defined as the absorbance of experimental samples, untreated samples, and blank controls, respectively. Untreated samples, defined as samples without any drug treatment, were used as negative controls.
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3

Cell Viability Assay with CCK-8 Kit

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Cell viability assays were measured using the Cell Counting Kit-8 kit (CCK-8, Dojindo laboratories, Kumamoto, Japan). In brief, cells were seeded in 96-well plates (5×103 cells per well) overnight. Cells pretreated with inhibitors (pifithrin-α or cystamine dihydrochloride) or transfected as described above with shRNA (control, TG2 or p53) were incubated with a series of concentrations of glucose culture medium. The cells were pretreated with NAC or ABT. After 48 h or 72 h, cell viability was evaluated by adding 10 μl of CCK-8 solution to each well of the plate. According to the manufacturer’s standard protocol, cell viability was measured using a BIO-TEK ELx800 Universal Microplate Reader (Bio-Tek, Winooski, VT, USA) by determining the absorbance (450 nm) after incubation for 2 h at 37°C. Cell viability was calculated using the formula: [(AE – AB)/(AC – AB)] × 100%. AE, AC, and AB were defined as the absorbance of experimental samples, untreated samples, and blank controls, respectively.
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4

Propranolol's Effect on HemSCs Viability

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Cell viability of HemSCs was measured by cell counting kit-8 kit (CCK-8, Sigma-Aldrich) as recommended [32 ]. In brief, HemSCs (104 per well) with different transfection were seeded into 24-well plate and subsequently treated with various concentrations of propranolol for 72 h. 10 μl CCK-8 reagent was added into each well with 2 h incubation. A BIO-TEK ELx800 Universal Microplate Reader (Bio-Tek, Winooski, VT, USA) was used for detection of the absorbance at 450 nm/630 nm. IC50 value for propranolol was calculated according to cell growth curves.
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