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6 mv linear accelerator

Manufactured by Siemens
Sourced in United States, Germany

The 6 MV Siemens linear accelerator is a medical device designed for the precise delivery of radiation therapy. It generates high-energy X-rays that can be directed at specific targets within the body. The device is capable of producing a beam of electrons or photons with an energy of up to 6 million electron volts (MV).

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22 protocols using 6 mv linear accelerator

1

Irradiation of Cell Samples

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Irradiation of the samples was performed at room temperature using a 6 MV Siemens linear accelerator (Siemens, Concord, CA) at a dose rate of 2 Gy min− 1. After exposure to IR, cells were further cultured in CGM for the indicated time until processing [24 (link)].
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2

Radiation Exposure Procedure for Cells

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Irradiation was performed at room temperature using a 6 MV Siemens linear accelerator (Siemens, Concord, CA) at a dose rate of 2 Gy/min. After irradiation, cells were kept in CGM for the indicated time until harvest.
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3

Radiation Exposure Protocol for Cells

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Irradiation was performed at room temperature using a 6 MV Siemens linear accelerator (Siemens, Concord, CA) at a dose rate of 2 Gy/min. After irradiation, cells were kept in CGM for the indicated time until harvest.
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4

ESCC Cell Line Radiation Exposure

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Human normal esophageal epithelial cells (HEEC) and Human ESCC cell lines, including ECA109, TE1, KYSE30, KYSE150, KYSE410, and KYSE450, were obtained from the Research Center of the Fourth Hospital of Hebei Medical University (Shijiazhuang, China). Cells were cultured in RPMI 1640 medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin and streptomycin at 37 °C incubator containing 5% CO2. The medium of cell lines was refreshed every 2 to 3 days. ESCC cells were exposed to X-ray irradiation by adopting the single energy 6-MV Siemens linear accelerator (Siemens, Buffalo Grove, IL, USA) at a 3 Gy/min dose-rate.
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5

X-irradiation Protocol using Siemens Accelerator

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X-irradiation was performed using a 6 MV Siemens linear accelerator (Siemens, Concord, CA, USA) with a dose rate of 2 Gy/min.
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6

Isolation and Irradiation of PBMCs

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The final cell density of isolated G0 unstimulated PBMCs was adjusted to 1 × 106 cells/ml and the samples were placed at 37 °C in a 5 % CO2 incubator. X-irradiation (0.5 and 2 Gy) was performed using a 6 MV Siemens linear accelerator (Siemens Concord, CA, USA) at a dose rate of 2 Gy/min. Non-irradiated cells were treated in similar way, but at a zero radiation dose.
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7

Radiation Exposure Protocol for Cells

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Irradiation was performed at room temperature using a 6 MV Siemens linear accelerator (Siemens, Concord, CA, USA) at a dose rate of 2 Gy/min. After irradiation, cells were kept in CGM for the indicated time until harvest.
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8

Siemens Linear Accelerator Irradiation

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Irradiation was performed at room temperature using a 6 MV Siemens linear accelerator (Siemens, Concord, CA) at a dose rate of 9.5 Gy/min.
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9

Culturing and Irradiating Human ESCC Cells

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Human ESCC lines (KYSE150, TE1, KYSE450, KYSE410, KYSE30 and ECA109) were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin at 37 °C and 5% CO2. All cells were obtained from the Research Center of the Fourth Hospital of Hebei Medical University.
ESCC cells were IR by a 6-MV Siemens linear accelerator (Siemens, Buffalo Grove, IL, USA) at room temperature. The total dose was 6/8/10 Gy, and the dose rate was 300 MU/min. The source-skin distance (SSD) was 100 cm, and cells were then collected at specific times for further study.
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10

FAM83D Regulates ESCC Radiosensitivity

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The human normal esophageal cell line HEEC was purchased from the Cellular Biology Institute of the Shanghai Academy of Sciences (Shanghai, China). The human ESCC cell lines ECA109 and TE1 were purchased from Procell Life Science & Technology Co., Ltd. (Wuhan, China). EC9706, KYSE30 and KYSE180 cell lines were purchased from Otwo Biotech Inc. (Shenzhen, China). The above cell lines were cultured in RPMI 1640 supplemented with 10% fetal bovine serum (FBS) at 37°C in 5% CO2. Plasmid containing the short hairpin RNA (shRNA) of FAM83D and the negative control (shNC) shRNA were purchased from GeneChem. Cells were seeded in 6-well plates and incubated for 24 h and transfected using Lipofectamine RNAiMAX (Invitrogen, USA) according to the manufacturer’s protocol. To obtain cells stably expressing FAM83D shRNA, G418 was added twenty-four hours after transfection, and stable transfectants were obtained after several weeks. Cells were irradiated at room temperature with a 6-MV Siemens linear accelerator (Siemens, Concord, CA) at a dose rate of 5 Gy/min after stable transfection and allowed to recover in an incubator for the indicated time until harvesting.
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