產(chǎn)品名稱 |
Renca |
商品貨號(hào) |
B167192 |
Organism |
Mus musculus, mouse |
Tissue |
kidney |
Cell Type |
epithelial |
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 |
renal adenocarcinoma |
Age |
6 weeks |
Gender |
male |
Storage Conditions |
liquid nitrogen vapor phase |
Images |
|
Derivation |
The Renca cell line was derived from a tumor that arose spontaneously as a renal cortical adenocarcinoma in Balb/cCr mice. |
Clinical Data |
male |
Tumorigenic |
YES |
Comments |
|
Complete Growth Medium |
The base medium for this cell line is RPMI-1640 (ATCC 30-2001). To make the complete growth medium, add the following components to the base medium:
- 10% Fetal Bovine Serum (BSA; ATCC 30-2020)
- Non-essential amino acids (NEAA; 0.1mM extra)
- Additional sodium pyruvate (1 mM extra)
- Additional L-glutamine (2 mM extra)
This medium is formulated for use with a 5% CO2 in air atmosphere. |
Subculturing |
Volumes used in this protocol are for 75 cm 2 flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
- Remove and discard culture medium.
- 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.
- 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 37°C to facilitate dispersal.
- Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
- Add appropriate aliquots of the cell suspension to new culture vessels. An inoculum of 2 X 104 to 4 X 104 viable cells/cm2 is recommended.
- Incubate cultures at 37°C. We recommend that you subculture when the culture reaches a cell concentration between 8 X 104 and 1.5 X 105 cells/cm2.
Subcultivation ratio: A subcultivation ratio of 1:4 to 1:10 is recommended.
Medium renewal: Every 2 to 3 days.
|
Cryopreservation |
Freeze medium: RPMI-1640 Medium, 77.5%; FBS, 15% FBS; DMSO, 7.5% Storage temperature liquid nitrogen vapor phase |
Culture Conditions |
Temperature: 37°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5% |
Population Doubling Time |
approximately 24 hours |
Name of Depositor |
R Wiltrout |
Year of Origin |
1969 |
References |
Murphy GP, Hrushesky WJ. A murine renal cell carcinoma. J. Natl. Cancer Inst. 50(4):1013-25, 1973. PubMed: 4703766
Salup RR, et al. Role of natural killer activity in development of spontaneous metastases in murine renal cancer. J. Urol. 134(6):1236-41, 1985. PubMed: 4057425
Engel J, et al. Transforming growth factor-beta type II receptor confers tumor suppressor activity in murine renal carcinoma (renca) cells . Urology. 54(1):164-70, 1999. PubMed: 10414746
|