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The TJ905 is a laboratory centrifuge designed for the separation of biological samples. It has a maximum speed of 15,000 rpm and a maximum relative centrifugal force (RCF) of 21,380 x g. The TJ905 can accommodate a variety of rotor sizes and configurations, allowing for versatile sample processing. Its precise temperature control and programmable settings make it suitable for a wide range of applications in life science research and clinical laboratories.

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5 protocols using tj905

1

Cell Culture Protocol for Glioblastoma

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Primary normal human astrocytes (NHAs) were purchased from Sciencell Research Laboratories (Carlsbad, CA, USA). Human U87, A172, U251, TJ905, and U373 glioblastoma cell lines were purchased from the ATCC (Manassas, VA, USA). NHAs were cultured in Dulbecco’s modified Eagle’s medium (DMEM), but all glioma cell lines were cultured in DMEM-F12; both mediums were supplemented with 10% fetal bovine serum (FBS). The mediums and FBS were purchased from Invitrogen (Carlsbad, CA). All cells were maintained in a 37°C, 5% CO2 incubator.
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2

Culturing Human Brain Cell Lines

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Normal human brain astroglia cell line SVGP12, normal human astrocyte (HA), glioma cell line TJ905, GOS-3, U87MG, and SHG-44 were obtained from ATCC (Manassas, VA, USA). SVGP12 and U87 were cultured in EMEM (Hyclone, USA). HA was cultured in Astrocyte Medium (ScienCell, USA). GOS-3 and TJ905 were cultured in DMEM (Hyclone, USA). SHG-44 was cultured in RPMI 1640 (Hyclone, USA) [27 (link)]. All cells were cultured in a medium supplemented with 10% FBS (Gibco, USA) at 37°C incubation with 5% CO2.
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Glioma Cell Line Culture Protocol

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Glioma cell lines U251, T98G, U87, TJ905 and U373 in the experiments were purchased from the ATCC. All cell lines were cultured in DMEM medium (HyClone) containing 10% FBS (Clark Bioscience) and stored in a humidified incubator at 37 °C with 5% CO2.
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4

Culturing Human Glial and Glioma Cells

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Human normal glial cell HEB and glioma cell lines (U87, TJ861, TJ905, U251, H4, and A172) were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA). The cells were cultured with RPMI1640 containing 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin (Invitrogen, CA, USA)) at 37℃ and 5% CO2. RPMI1640 and FBS were provided by Thermo Fisher Scientific (MA, USA). During the logarithmic growth phase, cells were treated with 0.25% trypsin (Thermo Fisher, HyClone, Utah, USA) for trypsinization and passage. It was found that CircPIP5K1A was the lowest expressed in U87 cells and the highest expressed in A172. Therefore, U87 and A172 cells were chosen as the research object in subsequent studies.
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5

Cell Line Authentication and Culture

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Human HEB and GBM cells (LN229, U251, U87, T98G, GOS3, and TJ905) were purchased from American Type Culture Collection (ATCC). These cells were authenticated using an STR assay (Beijing Genomics institution). HEB, LN229, U251, U87, GOS3, and TJ905 cells were cultured in DMEM containing 10% FBS (Clark Bioscience, Australia); T98G cells were cultured in MEM containing NEAA and 10% FBS (Clark Bioscience, Australia) and grown in a humidified incubator at 37 °C in an atmosphere of 5% CO2.
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