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The HKBMM is a laboratory equipment designed for the analysis and separation of biological macromolecules. It utilizes high-performance liquid chromatography (HPLC) technology to perform efficient and precise biomolecule purification. The core function of the HKBMM is to facilitate the isolation and characterization of proteins, nucleic acids, and other relevant biomolecules from complex samples.

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2 protocols using hkbmm

1

Establishing Meningioma Cell Lines

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HKBMM, a human malignant meningioma cell line, was obtained from the Riken BioResource Research Center (Tsukuba, Japan) and maintained in Ham’s F12 medium supplemented with 10% fetal bovine serum (FBS). IOMM-Lee, a human malignant meningioma cell line, and IMR90, normal human fetal lung fibroblasts, were obtained from the American Type Culture Collection (Manassas, VA, USA) and cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FBS. M-20-U, M-10-S, and M-16-N were established by H.H. from the brain tumor tissues of benign meningiomas (M-20-U and M-10-S) and an atypical meningioma (M-16-N), as described in detail in the Supplementary Materials and Methods, and were maintained in RPMI-1640 medium supplemented with 20% FBS.
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2

Culturing IMR90, IOMM-Lee, and HKBMM cell lines

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IMR90, normal human fetal lung fibroblasts, and IOMM-Lee, a human malignant meningioma cell line expressing wild-type p53, were obtained from the American Type Culture Collection (Manassas, VA, USA) and cultured in Dulbecco’s modified Eagle’s medium supplemented with 10% or 5% fetal bovine serum (FBS), respectively. HKBMM, a human malignant meningioma cell line expressing a mutant p53 (P177L), was obtained from the Riken BioResource Research Center (Tsukuba, Japan) and maintained in Ham’s F12 medium supplemented with 10% FBS. The culture media were supplemented with 100 U/mL penicillin and 100 μg/mL streptomycin. The p53 status of IOMM-Lee and HKBMM cells was examined by cDNA sequencing as described below. IMR90 cells passaged fewer than 8 times were used in experiments. Detailed conditions for the in vitro drug treatment are described in the respective figure legends. In general, the day after cells had been passaged, the required amount of the drug stock solution was added to cells and gently mixed well. This was followed by an incubation at 37 °C in a 5% CO2 incubator for the specified time, and cells were then subjected to each assay.
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