GIMEN cell

SKU:BHC11100523
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Overview
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GIMEN cell is a cell line derived from Caucasian (Female). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Epithelial-like. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Neuroblastoma
Morphology Epithelial-like
Growth Properties Adherent
Tissue Brain
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Catalog no. Size
300179 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
Mfr No 300179
Species Human
The GIMEN cell line is derived from the bone marrow metastasis of a young child diagnosed with stage IV neuroblastoma. These cells are classified as N-type, which typically indicates a neuroblastic phenotype characterized by high cell density, neuronal properties, and the capability for extensive neurite outgrowth in culture. The establishment of the GIMEN cell line provides a valuable model for studying the molecular and cellular mechanisms underlying aggressive forms of neuroblastoma, particularly those associated with metastatic dissemination. Functionally, GIMEN cells exhibit notable interactions with various cytokines and growth factors. Specifically, their growth is inhibited by interferon-gamma (IFN-gamma), a cytokine known for its antiproliferative effects on certain cancer cells. Furthermore, fibroblast growth factor-2 (FGF-2) demonstrates an antimitogenic effect on these cells, which can be reversed by the addition of IFN-gamma. This reversal suggests a complex interplay between these factors in modulating cell proliferation. Additionally, interleukin-1 beta (IL-1 beta) enhances the antimitogenic effects of FGF-2, indicating its potential role in the regulation of tumor growth dynamics in the neuroblastoma microenvironment. These interactions highlight the GIMEN cell line's utility in exploring the impact of cytokines and growth factors on neuroblastoma progression and response to therapy.

SKU:BHC11100523

  • 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
  • doublingTime: 25 hours
  • 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: 2 to 3 x 104 cells/cm2
  • fluidRenewal: 2 to 3 times per week
  • freezeMedium: As a cryopreservation medium, use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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