U-138 MG cell

SKU:BHC11100542
Bulk Pricing Research Validated
Overview
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U-138 MG cell is a cell line derived from Caucasian (Male). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Polygonal. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Astrocytoma
Morphology Polygonal
Growth Properties Adherent
Tissue Brain
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Catalog no. Size
300363 1 cryovial
Available Options

This cell line is available in the U.S. For non-profit users, please sign and submit the Non-Profit Supply Agreement to orders@biohippo.com before placing an order. For commercial users, please complete the CLEAR Form before ordering, as additional usage fees may apply based on the intended use. For further details, please contact orders@biohippo.com. Products ship after the required agreement is completed; typical delivery is 2–3 business days. Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10^6 cells for adherent lines or 5 × 10^6 cells for suspension lines (refer to the batch CoA for details).

Field Specification
Cellosaurus CVCL_0020
Species Human
Applications
  • Cell Culture (Growth)
  • Functional Assay
Classification Brain cancer cell lines
Tissue
  • Brain
Disease Astrocytoma
Age 47 years
Sex Male
Ethnicity Caucasian
Growth properties
  • Adherent
Biosafety level 1
Catalog no. (Mfr.) 300363
Main SKU BHC11100542
This is one of a number of cell lines derived from malignant gliomas, e.g. U-87-MG, U-118-MG and U-373-MG isolated by J. Ponten and associates from 1966 to 1969. It differs from U-87-MG in morphology and it has a slower proliferation rate. U-138-MG shows strong similarity to U-118-MG, sharing at least six derivative marker chromosomes.

SKU:BHC11100542

  • Antigen expression: Blood Type A, Rh+
  • Isoenzymes: Me-2, 1, PGM1, 1, PGM3, 1, ES-D, 1, AK-1, 1, GLO-1, 1-2, G6PD, B,
  • Karyotype: Hyperdiploid to pentaploid with several markers, the stemline chromosome number is near triploid with the 2S component occurring at 9.8%. Five markers [t(11,5), t(8q,4), t(19,?18), M1 and M2] were common to most S metaphases. One chromosome 4 could be found in every S metaphase. Chromosome composition was very uniform among cells. Phenotype Frequency Product: 0.0511
  • cultureMedium: DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a)
  • supplements: Supplement the medium with 10% FBS
  • dissociationReagent: Accutase
  • subculturing: Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
  • seedingDensity: 1 x 104 cells/cm2
  • fluidRenewal: 2 to 3 times per week
  • freezeMedium: As a cryopreservation medium, use 50% basal medium + 40% FBS + 10% DMSO, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
  1. MACC1 driven alterations in cellular biomechanics facilitate cell motility in glioblastomaCell Communication and Signaling : CCS| DOI: 10.1186/s12964-020-00566-1 | PMID: 32503676 | PMC: pmc07275321
  2. Synthetic Cannabinoids Influence the Invasion of Glioblastoma Cell Lines in a Cell- and Receptor-Dependent MannerCancers| DOI: 10.3390/cancers11020161 | PMID: 30709059 | PMC: pmc06406558
  3. Integrative analysis of therapy resistance and transcriptomic profiling data in glioblastoma cells identifies sensitization vulnerabilities for combined modality radiochemotherapyRadiation Oncology (London, England)| DOI: 10.1186/s13014-022-02052-z | PMID: 35440003 | PMC: pmc09020080
  4. The Spheroid Light Microscopy Image Atlas for morphometrical analysis of three-dimensional cell culturesScientific Data| DOI: 10.1038/s41597-025-04441-x | PMID: 39962061 | PMC: pmc11833042
  5. Jamming Transitions in Astrocytes and Glioblastoma Are Induced by Cell Density and TensionCells| DOI: 10.3390/cells12010029 | PMID: 36611824 | PMC: pmc09818602
  6. On the influence of cannabinoids on cell morphology and motility of glioblastoma cellsPLoS ONE| DOI: 10.1371/journal.pone.0212037 | PMID: 30753211 | PMC: pmc06372232
  7. The influence of biomechanical properties and cannabinoids on tumor invasion.Cell adhesion & migration| DOI: 10.1080/19336918.2016.1183867 | PMID: 27149140 | PMC: pm27149140
  8. Effects of tumor treating fields (TTFields) on glioblastoma cells are augmented by mitotic checkpoint inhibitionCell Death Discovery| DOI: 10.1038/s41420-018-0079-9 | PMID: 30210815 | PMC: pmc06125382
  9. An optimized protocol for metabolic measurement in 3D tumor spheroids derived from primary and established glioblastoma cellsPLOS One| DOI: 10.1371/journal.pone.0347569 | PMID: 42030290 | PMC: pmc13108750
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