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是否是腫瘤細胞：1
物種來源：人
細胞形態(tài)：上皮樣
數(shù)量：大量
器官來源：肺
生長狀態(tài)：貼壁生長
ATCC Number：CRL-5941?
相關(guān)疾?。悍切〖毎伟?br /> 年限：stage 3A
運輸方式：凍存運輸
規(guī)格：0.1ml Designations: NCI-H2342 [H2342]
Depositors: ?AF Gazdar, JD Minna
Biosafety Level:1
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
Organism: Homo sapiens
Morphology:epithelial


Source: Organ: lung
Tumor Stage: stage 3A
Disease: adenocarcinoma; non-small cell lung cancer
Permits/Forms:In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
Restrictions:The line is available with the following restrictions: 1. This cell line was deposited at the ATCC by Dr. A. Gazdar and Dr. J. Minna and is provided for research purposes only. Neither the cell line nor products derived from it may be sold or used for commercial purposes. Nor can the cells be distributed to third parties for purposes of sale, or producing for sale, cells or their products. The cells are provided as service to the research community. They are provided without warranty of merchantability or fitness for a particular purpose or any other warranty, expressed or implied. 2. Any proposed commercial use of the these cells, or their products must first be negotiated with the University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, Texas 75235. Telephone (214) 699-8056, FAX (214) 688-7233.
DNA Profile (STR):Amelogenin: X,Y
CSF1PO: 10
D13S317: 12
D16S539: 13
D5S818: 12
D7S820: 10
THO1: 9,9.3
TPOX: 8,10
vWA: 17
Age: 55 years
Gender: male
Ethnicity: Caucasian
Comments:The line was established in April 1990.
The tissue donor was a non-smoker.
Propagation: ATCC complete growth medium: HITES medium supplemented with 5% fetal bovine serum

The base medium for this cell line is ATCC-formulated DMEM:F12 Medium Catalog No.30-2006. To make the complete growth medium,add the following components to the base medium
1. 0.005 mg/ml Insulin
2. 0.01 mg/ml Transferrin
3. 30nM Sodium selenite (final conc.)
4. 10 nM Hydrocortisone (final conc.)
5. 10 nM beta-estradiol (final conc.)
6. extra 2mM L-glutamine (for final conc. of 4.5 mM)
7. 5% fetal bovine serum (final conc.)

Temperature: 37.0°C
Subculturing: Protocol: Volumes used in this protocol are for 75 sq cm flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.

1. Remove and discard culture medium.
2. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) or 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
3. Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
   Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37C to facilitate dispersal.
4. Add 2.0 to 3.0 ml of complete growth medium and aspirate cells by gently pipetting
5. Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to new culture vessels.
6. Incubate cultures at 37C.
   Subcultivation Ratio: 1:2 to 1:6.

Preservation: Culture medium, 95%; DMSO, 5%
Related Products:Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2006
References: 23570: . NCI-Navy Medical Oncology Branch Cell Line Supplement. J. Cell. Biochem. suppl. 24: 1996..