ArtNr |
CLS-300423 |
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 |
Human (Homo sapiens) |
Dry ice |
Yes
|
ECLASS 10.1 |
42040401 |
ECLASS 11.0 |
42040401 |
UNSPSC |
41106509 |
Alias |
SK-Mel-2, SK-Mel 2, SK-mel-2, SK-MEL2, SK.MEL.2, SK Mel 2, SK MEL 2, SKMEL-2, SKMEL2, SKmel2, SK-ML2, SKml2 |
Lieferbar |
|
Manufacturer - Category |
Skin cancer cell lines | Human cells |
Description |
Introducing SK-MEL-2 cells, a cell line derived from a 60-year-old, White, male patient with malignant melanoma. These cells express wildtype B-Raf and mutant N-Ras (Q61R). With a doubling time of 32 hours, SK-MEL-2 cells provide a valuable tool for studying melanoma. Melanoma arises when mutations occur in melanocytes, leading to uncontrolled multiplication and cancer development. By using SK-MEL-2 cells, researchers can gain insights into melanoma's mechanisms and explore potential treatments. |
Tissue |
Skin |
Growth properties |
Adherent |
Disease |
Melanoma |
Age |
60 years |
Gender |
Male |
Ethnicity |
Caucasian |
Morphology |
Polygonal |
Biosafety Level |
1 |
Culture Medium |
DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 1.5 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
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 |
2 to 3 times per week |
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 |
Tumorigenic |
Yes, in nude mice. Forms malignant melanoma |
Split Ratio |
A ratio of 1:3 to 1:6 is recommended |
Seeding Density |
1 x 10^4 cells/cm^2 |
Metastatic Site |
Skin of thigh |
Karyotype |
(P6) hypodiploid to hypertetraploid with abnormalities including dicentrics, secondary constrictions and large telocentric marker. Phenotype Frequency Product: 0.0742 |
Isoenzymes |
PGM3, 1, PGM1, 1, ES-D, 1, AK-1, 1, GLO-1, 2, G6PD, B |
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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.