產品名稱 |
VMM425 |
商品貨號 |
B222637 |
Organism |
Homo sapiens, human |
Tissue |
Melanoma, Pelvic Soft Tissue Metastasis |
Cell Type |
Melanocyte |
Product Format |
frozen |
Morphology |
Epithelial-like |
Culture Properties |
adherent |
Biosafety Level |
1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
Disease |
Melanoma, Stage IV; malignant |
Age |
60 |
Gender |
Male |
Ethnicity |
Caucasian |
Applications |
Drug screening
Development of targeted therapy
Development of combination therapy
Tumor vaccine development |
Storage Conditions |
liquid nitrogen vapor phase |
Images |
|
Derivation |
Derived from a pelvic soft tissue recurrence. Established from digest of Right Pelvic Tumor Metastasis in PETI Medium. |
Clinical Data |
Primary Site: Left Foot (Plantar); Metastatic Site: Pelvic Soft Tissue |
HLA Typing |
A2,A31,B7,B51,Cw7?,Cw16?,DR4(DRB1*0404),[DR11(DRB1*1101) or DR13(DRB1*131401)],DR52(DRB3*0202),DR53(DRB4*0103) |
Comments |
NRAS Mutation: Q61L Q61R
CDKN2A: wt
BRAF: wt
PET Scan + |
Complete Growth Medium |
The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, ATCC 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (ATCC 30-2020) to a final concentration of 10%.
|
Subculturing |
Volumes are for a T-75 flask; Adjust accordingly
- Remove and discard the cell culture medium from the flask.
- Rinse the cell monolayer with Dulbecco’s PBS without calcium or magnesium and remove.
- Add 3 to 4 ml of the trypsin-EDTA solution, rotate flask to rinse cell monolayer, remove trypsin solution, and incubate at 37oC.
- Once the cells appear to be detached, add 10 ml of complete growth medium with a pipette to
the cell suspension to inactivate the trypsin. Gently wash any remaining cells from the growth surface of the flask. Check the cells with the microscope to be sure that most (>95%) are single cells. If cell clusters are apparent, continue to disperse the cells with gentle pipetting.
- Subculture as necessary.
- Place the flask back into the incubator. Examine the culture the following day to ensure the cells have reattached and are actively growing.
- Repeat when cells reach ~ 50-75% confluence.
CELLS DO NOT GET CONFLUENT |
Cryopreservation |
Fetal bovine serum, 90%; DMSO, 10% |
Culture Conditions |
Temperature: 37°C
Atmosphere: air, 95%; carbon dioxide (CO2
), 5% |
STR Profile |
Amelogenin: X
D5S818: 11
D13S317: 9,13
D7S820: 9
D16S539: 12
vWA: 17,19
TH01: 8,9.3
TPOX: 8,12
CSF1PO: 12
|
Sterility Tests |
Pass |
Population Doubling Level (PDL) |
unknown |
Population Doubling Capacity |
unknown |
Name of Depositor |
Craig L. Slingluff, Jr. M.D. |
Passage History |
Original deposit at one passage from the primary culture |
Year of Origin |
2007 |
References |
Molhoek K, et al. Comprehensive analysis of RTK activation in human melanomas reveals autocrine signaling through IGF-1R. Melanoma Res 21(4): 274–284, 2011. PubMed: 21654344
|