C8-D1A cell

SKU:BHC11101231
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Overview
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C8-D1A cell is a Astrocyte cell line (Unspecified). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Neuronal. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Mouse
Morphology Neuronal
Growth Properties Adherent
Tissue Brain
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).

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Catalog no. Size
300316 1 cryovial
Field Specification
Species Mouse
The C8-D1A cell line is an astrocyte cell line derived from the cerebral cortex of an 8-day-old C57BL/6 mouse. This cell line is extensively used in neurobiological research due to its robust astrocytic properties, which make it a representative model for studying various aspects of astrocyte function and neuron-glia interactions. The C8-D1A cells express glial fibrillary acidic protein (GFAP), a hallmark intermediate filament protein of mature astrocytes, indicating their differentiated state and astrocytic lineage. Research utilizing the C8-D1A cell line has contributed significantly to understanding neuroinflammatory responses, glial scar formation, and the role of astrocytes in neurotransmitter regulation and synaptic maintenance. These cells provide a consistent and controlled in vitro environment for dissecting molecular pathways involved in neurodegeneration, CNS injuries, and astrocyte-mediated neuroprotection. Their utility in assays related to drug discovery, particularly for neurological disorders, underscores their importance in therapeutic development processes.

SKU:BHC11101231

  • 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.
  • 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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