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VMM425
VMM425
規(guī)格:
貨期:
編號(hào):B222637
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 VMM425
商品貨號(hào) 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 ATCC CRL-3231 Cell Micrograph
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

  1. Remove and discard the cell culture medium from the flask.
  2. Rinse the cell monolayer with Dulbecco’s PBS without calcium or magnesium and remove.
  3. Add 3 to 4 ml of the trypsin-EDTA solution, rotate flask to rinse cell monolayer, remove trypsin solution, and incubate at 37oC.
  4. 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.
  5. Subculture as necessary.
  6. Place the flask back into the incubator. Examine the culture the following day to ensure the cells have reattached and are actively growing.
  7. 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

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于經(jīng)理 18067160830 2088210172
沈經(jīng)理 19548299266 2662369050
李經(jīng)理 13626845108 972239479
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