Vergleich

PC-12 adherent Europäischer Partner

Für die Verwendung dieses Produktes fordert der Hersteller das zu Ihrer Institution passende, ausgefüllte und unterschriebene Formular: Bitte laden Sie dieses entweder beim Kaufabschluss hoch oder senden es alternativ an die purchasing@hoelzel.de
ArtNr CLS-500311
Hersteller CLS Cell Lines Service
Menge 1 cryovial
Kategorie
Typ Cell line
Zertifikat For a certificate of analysis, please send an inquiry to info@hoelzel.de.
Specific against Rat (Rattus norvegicus)
Dry ice Yes
ECLASS 10.1 42040401
ECLASS 11.0 42040401
UNSPSC 41106509
Alias PC 12,PC12
Lieferbar
Manufacturer - Category
Rat cell lines
Description
PC-12 cells are a cell line derived from a pheochromocytoma of the rat adrenal medulla. These cells are of embryonic origin, grow adherently and resemble a mixture of neuroblastic and eosinophilic cells. PC-12 cells are catecholamine cells that synthesize, store and release norepinephrine and dopamine. They have a diameter of approximately 10-12 microns and are small, irregularly shaped cells. The PC12 cell line is a classical neuronal cell model due to its ability to acquire sympathetic neuron features when dealing with nerve growth factor (NGF).
Studies on dopamine regulation have shown that PC12 cells synthesize, release, and reuptake dopamine and have been extensively characterized for neurosecretion and the presence of ion channels and neurotransmitter receptors. Moreover, the relative proportion of various subtypes of Ca channels changes during differentiation. The PC12 cell line is an established neuronal cell model that is particularly useful in studying cellular responses to nerve growth factors (NGF) and how these lead to the expression of differentiation-specific proteins and differentiation. When cultured in NGF, PC12 cells differentiate into sympathetic ganglion neurons morphologically and functionally. The differentiation results from the reversible induction of a neuronal phenotype by NGF. Collagen coating has been shown to be favourable to achieving neuronal characteristics in terms of length and density of neurites by NGF treatment.
PC12 cells are tumorigenic and were derived from male New England Deaconess Hospital strain rats. The PC-12 cell line has 40 chromosomes, 38 autosomes, plus xY. Nerve growth factor (NGF) is expressed in PC12 cells, and exposure to NGF is one crucial regulator of cell differentiation.
In conclusion, PC12 cells are a versatile and widely used model system in neurobiology due to their ability to acquire sympathetic neuron features when dealing with nerve growth factor (NGF). These cells have been extensively characterized for neurosecretion, ion channels, and neurotransmitter receptors. Their extreme versatility for pharmacological testing and use as an established model for studying the proliferation and differentiation of neuronal cells make them a valuable tool in neurobiology research.
Tissue
Adrenal gland
Growth properties
Small clusters in suspension, poorly adherent, patches on collagen.
Disease
Pheochromocytoma
Age
Unspecified
Gender
Male
Ethnicity
Japanese
Morphology
Polygonal
Biosafety Level
1
Culture Medium
RPMI 1640, w: 2.1 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
Medium Supplements
Supplement the medium with 10% FBS
Subculturing
Suspension cells: Remove cells from substrate by pipetting with fresh medium. To obtain single cells, pass the suspension several times through a 22 gauge needle and dispense into new flasks. Growing on collagen: To remove adherent cells, use the following standard protocol. Remove medium and rinse the adherent cells using PBS without calcium and magnesium (3-5 ml PBS for T25, 5-10ml for T75 cell culture flasks). Add TrypleExpress (1-2ml per T25, 2.5ml per T75 cell culture flask), the cell sheet must be covered completely. Incubate at 37 degree Celsius for 10 minutes. Carefully resuspend the cells, the addition of medium is optional but not necessary, and dispense into new flasks which contain fresh medium.
Fluid Renewal
2 to 3 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 48 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.
Tumorigenic
Yes, in New England Deaconess Hospital strain rats
Split Ratio
A ratio of 1:3 to 1:8 is recommended
Seeding Density
1 x 10^4 cells/cm^2
Products
Catecholamines, dopamine
Karyotype
40 chromosomes, 38 autosomes plus XY
Receptors Expressed
Nerve growth factor (NGF)

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
lieferbar

Vergleichen

Auf den Wunschzettel

Angebot anfordern

Lieferzeit anfragen

Technische Frage stellen

Bulk-Anfrage stellen

Fragen zum Produkt?
 
Schließen