C8-D1A Cells

Name: CLS Cell Lines Service GmbH
Address: Dr.-Eckener-Straße 8, Eppelheim, 69214, DE
Telephone: +496221405780
Price range: €€€

USD$395.00*

Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10⁶ cells for adherent lines or 5 × 10⁶ cells for suspension lines (refer to the batch CoA for details).

Prices excl. taxes plus shipping costs

cryovial

Product number: 300316

Safety data sheet

Product sheet

Certificate of Analysis (CoA)

Description	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.
Organism	Mouse
Tissue	Brain
Applications	3D cell culture, Neuroscience
Synonyms	C8D1A, Astrocyte type I clone

Breed/Subspecies	C57BL/6
Age	8 days
Gender	Unspecified
Morphology	Neuronal
Cell type	Astrocyte
Growth properties	Adherent

Citation	C8-D1A (Cytion catalog number 300316)
Biosafety level	1
NCBI_TaxID	10090
CellosaurusAccession	CVCL_6379

Ploidy status	Pseudodiploid

Culture Medium	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
Dissociation Reagent	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.
Freeze medium	As a cryopreservation medium, we 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.
Thawing and Culturing Cells	Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.
Incubation Atmosphere	37°C, 5% CO₂, humidified atmosphere.
Shipping Conditions	Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.
Storage Conditions	For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.

Sterility	Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.

Lot Number	Certificate Type	Date	Catalog Number
300316-280425	Certificate of Analysis	23. May. 2025	300316
300316-201023	Certificate of Analysis	23. May. 2025	300316

C8-D1A Cells

General information

Characteristics

Regulatory Data

Biomolecular Data

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Quality Control & Molecular Analysis

Certificate of Analysis (CoA)