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Arpe 19 cells

Manufactured by Procell
Sourced in China

ARPE-19 cells are a human retinal pigment epithelial cell line. They are derived from the normal eye tissue of a human donor and are commonly used in scientific research. ARPE-19 cells exhibit characteristics of retinal pigment epithelial cells and can be utilized for various in vitro studies.

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4 protocols using arpe 19 cells

1

Investigating Retinal Cell Response to Color Spectra

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We carried out cellular experiments to investigate the effects of different spectrums. The retinal cells for this study were human ARPE-19 cells purchased from Procell Co. Ltd. We cultivated the ARPE-19 cells with the DMEM-F12 solution (10% fetal-calf serum) in the cell-culture incubator with 5% CO2. All the ARPE-19 cells were divided into three groups and cultivated in the screen with the three color-deviation levels shown in Table 1. The screens were set to the status of white balance, and the illuminance value was 400 lux.
For CV measurement, we performed cellular staining with the Trypan Blue and then analyzed the CV using the ThermoFisher Scientific Flow Cytometer instrument. CV data were automatically collected.
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2

Culturing ARPE-19 Cells for Experiments

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ARPE-19 cells (Procell Life Science & Technology Co., Ltd., certified by STR) were maintained in DMEM/F-12 supplemented with 10% FBS, streptomycin (100 mg/ml) and penicillin (100 U/ml), at 37°C with 5% CO2. All treatments were performed when the cells reached ~80% confluence.
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3

ARPE-19 Cell Culture and Glucose Treatment

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ARPE-19 cells are purchased from procell Life Technology Co., Ltd. (Wuhan, China). The complete culture medium for ARPE-19 cells consisted of Dulbecco’s modified Eagle’s medium (DMEM)/F-12 (volumetric ratio of 1:1; HyClone, Logan, UT, USA) and 10% fetal bovine serum (FBS; HyClone). ARPE-19 cells were cultured at 37°C in humidified air with 5% CO2. For treatment, ARPE-19 cells were grown in complete culture medium until approximately 75% confluence. Subsequently, the culture medium was replaced with FBS-free DMEM/F-12 for 24 h before switching to high glucose (60 mM D-glucose) or normal glucose (NG) (5.5 mM D-glucose) conditions. The cell culture medium was not renewed during the 48 h high glucose and normal glucose treatment. When the cells were routinely cultured, the medium was renewed every other day.
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4

ARPE-19 Cells Culture Protocol

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ARPE-19 cells were purchased from Procell Life Science & Technology Co. Ltd., China (#CL-0026; preservation institution: ATCC, CRL-2302, BCRC), cultured in 90% dulbecco’s modified eagle medium (DMEM, #PM150210; Procell) with 10% FBS (#164210-500; Procell) at 37°C and 5% CO2. Fer-1 (#T6500; Target Molecule Corp., Boston, MA, USA), erastin (#T1765; TargetMol), AS-IV (#HY-N0431; MCE, USA), and EX 527 (#T6111; TargetMol) were used in the experiments.
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