CRL-1715 TM4 正常小鼠睪丸Leydig細胞，ATCC 細胞|細胞系|細胞株|腫瘤細胞|細胞|；細胞庫管理規范，提供的細胞株背景清楚，提供參考文獻和*培養條件！
CRL-1715 TM4 正常小鼠睪丸Leydig細胞 的詳細介紹
CRL-1715 TM4 正常小鼠睪丸Leydig細胞
| ATCC? Number: | CRL-1715? | Price: | $329.00 |
| Designations: | TM4 | | Depositors: | JP Mather | | Biosafety Level: | 1 | | Shipped: | frozen | | Medium & Serum: | See Propagation | | Growth Properties: | adherent | | Organism: | Mus musculus （mouse） | | Morphology: | epithelial
| | Source: | Organ: testis
Disease: normal
Cell Type: Sertoli cell; | | Cellular Products: | retinol binding protein
tissue plasminogen activator
transferrin | | 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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location. |
| | Applications: | transfection host （Roche FuGENE? Transfection Reagents） | | Receptors: | follicle stimulating hormone （FSH）, expressed
androgen receptor, expressed
progesterone receptor, expressed | | Tumorigenic: | No | | Antigen Expression: | H-Y antigen; Mus musculus, expressed | | Age: | 11 to 13 days | | Gender: | male | | Comments: | The TM4 cell line is reported to respond to FSH with an increase in cAMP production, but to not respond to luteinizing hormone （LH）. The FSH responsiveness is much reduced compared to primary sertoli cell cultures. Constitutive plasminogen activator production is reported to be low, but is stimulated by FSH and, to a greater extent, by retinoic acid.
Tested and found negative for ectromelia virus （mousepox）. | | Propagation: | ATCC complete growth medium: A 1:1 mixture of Ham'S F12 medium and Dulbecco's modified Eagle's medium with 1.2 g/L sodium bicarbonate and 15 mM HEPES, 92.5%; horse serum, 5%; fetal bovine serum, 2.5%
Atmosphere: air, 95%; carbon dioxide （CO2）, 5%
Temperature: 37.0°C | | Subculturing: | Protocol: - Remove and discard culture medium.
- Briefly rinse the cell layer with 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 37C 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 supension to new culture vessels.
- Incubate cultures at 37C.
Subc*tion Ratio: A subc*tion ratio of 1:10 to 1:50 is recommended
Medium Renewal: Every 3 to 4 days | | Preservation: | Freeze medium: Culture medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase | | Related Products: | Recommended medium （without the additional supplements or serum described under ATCC Medium）:ATCC 30-2006
recommended serum:ATCC 30-2020
recommended serum:ATCC 30-2040 | | References: | 1158: Mather JP. Establishment and characterization of two distinct mouse testicular epithelial cell lines. Biol. Reprod. 23: 243-252, 1980. PubMed: 6774781
1159: Mather JP, et al. Culture of testicular cells in hormone-supplemented serum-free medium. Ann. N.Y. Acad. Sci. 383: 44-68, 1982. PubMed: 7046561
1184: Carson DD, et al. Synthesis and secretion of a novel binding protein for retinol by a cell line derived from Sertoli cells. J. Biol. Chem. 259: 3117-3123, 1984. PubMed: 6538197
26150: Mather JP, Phillips DM. Establishment of a peritubular myoid-like cell line and interactions between established testicular cell lines in culture. J. Ultrastruct. Res. 87: 263-274, 1984. PubMed: 6544874 |
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