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Neuro-2a Cells Europäischer Partner

ArtNr CLS-400394
Hersteller CLS Cell Lines Service
Menge 1 cryovial
Kategorie
Typ Cell line
Zertifikat The certificate of analysis can be requested on the website or via email at info@cytion.com. Please indicate the lot number of your product in the email.
Specific against Mouse (Murine, Mus musculus)
Dry ice Yes
ECLASS 10.1 42040401
ECLASS 11.0 42040401
UNSPSC 41106509
Alias NEURO-2A, Neuro 2a, Neuro2a, Neuro2A, N-2a, N2a, N2A, Nb2a, NB2a
Lieferbar
Manufacturer - Category
Mouse cell lines
Description
The Neuro-2a cell line, often abbreviated as N2A cells, is a mouse neuroblastoma cell line derived from the neural crest. These cells are known for their rapid proliferation and ability to differentiate into neuron-like cells under certain conditions, making them a valuable model for studying neurogenesis and neuronal differentiation. Neuro-2a cells exhibit characteristics typical of nerve cells or neuroblasts, which are precursors to fully differentiated neuronal cells.
One of the key features of mouse Neuro 2a cells is their utility in exploring the mechanisms of differentiation, particularly in the context of dopaminergic neurons. These cells can be induced to express markers characteristic of dopamine neurons, including the dopamine transporter and proteins involved in dopamine receptor localization. This makes the N2A cell line an essential tool for studies related to the normal neuroendocrine system and disorders associated with dopaminergic signaling.
The N2A cell line also provides insights into the role of various genes and proteins in neuronal function and development. For instance, the DNMT3A gene, known for its involvement in DNA methylation processes, has been studied in Neuro-2a cells to understand its impact on neuronal cells and neurodevelopmental processes. The expression of the human thyroid hormone receptor in these cells allows researchers to investigate thyroid hormone response and its influence on neurodevelopment and the differentiation of neuroblastoma cells into more mature neuronal phenotypes. Protein kinase signaling pathways are another area of intense study in N2A cells, given their critical role in mediating various cellular processes, including cell growth, differentiation, and response to extracellular signals.
In summary, the Neuro-2a (N2A) cell line, derived from mouse neuroblastoma, serves as a versatile model for studying neurogenesis, neuronal differentiation, and dopaminergic signaling, providing valuable insights into the molecular underpinnings of neurodevelopmental processes and neuroendocrine disorders.
Growth properties
Adherent
Cell type
Neuronal and amoeboid stem cells
Disease
Neuroblastoma
Breed
A/J
Biosafety Level
1
Viruses
Ectromelia virus (mousepox): negative
Culture Medium
EMEM, w: 2 mM L-Glutamine, w: 1.5 g/L NaHCO3, w: EBSS, w: 1 mM Sodium pyruvate, w: NEAA (Cytion article number 820100c)
Medium Supplements
Supplement the medium with 10% FBS
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.
Fluid Renewal
1 to 2 times per week
Freezing Recovery
After thawing, plate the cells at 5 x 10^4 cells/cm^2 and allow the cells to recover from the freezing process and to adhere for at least 24 hours.
Freeze Medium
Handling of Cryopreserved Cultures

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.

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.
Safety Precautions
When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments.
Disclaimer
Our cells are provided for in vitro laboratory research purposes exclusively and are not intended for clinical or diagnostic use, nor are they to be administered to humans or used for veterinary purposes. Users must adhere to all applicable guidelines and regulations for the handling and use of these cells in a research setting.
Warranty
We stand by the promise of delivering products with high cell viability and robust culture performance. To achieve the best results, please make sure you follow the storage and culture instructions detailed in the product information sheet closely. Your adherence to these guidelines is key to success.
Amelogenin
X, X
Split Ratio
A ratio of 1:4 is recommended
Seeding Density
1 x 10^4 cells/cm^2
Antigen Expression
H-2a
Reverse Transcriptase
Negative
Products
Tubulin, acetylcholinesterase
Virus Resistance
Poliovirus 1
NOTE
Deutsch:
Universitäre Kunden: Für den Erwerb ist ein Material Transfer Agreement oder eine Limited Use Label License auszufüllen.
Kommerzielle Kunden: Für den Erwerb ist ein Material Transfer Agreement oder ein Master Supply Agreement auszufüllen.
Nach eingegangener Bestellung werden ihnen alle relevanten Dokumente zugeschickt.

English:
University Customers: A Material Transfer Agreement or Limited Use Label License must be completed for purchase.
Commercial Customers: A Material Transfer Agreement or Master Supply Agreement must be completed for purchase.
After the order is received, all relevant documents will be sent to you.

Hinweis: Die dargestellten Informationen und Dokumente (Bedienungsanleitung, Produktdatenblatt, Sicherheitsdatenblatt und Analysezertifikat) entsprechen unserem letzten Update und sollten lediglich der Orientierung dienen. Wir übernehmen keine Garantie für die Aktualität. Für spezifische Anforderungen bitten wir Sie, uns eine Anfrage zu stellen.

Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 1 cryovial
Lieferbar: In stock
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