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- 文献和实验
- 技术资料
- 细胞形态:
多边形
- 相关疾病:
恶性黑色素瘤
- ATCC Number:
HTB-68™
- 生长状态:
贴壁生长
- 库存:
大量
- 运输方式:
冻存运输
- 器官来源:
皮肤
- 年限:
60 years
- 物种来源:
人
- 是否是肿瘤细胞:
1
| Designations: | SK-MEL-2 | ||
| Depositors: | G Trempe, LJ Old | ||
| Biosafety Level: | 1 | ||
| Shipped: | frozen | ||
| Medium & Serum: | See Propagation | ||
| Growth Properties: | adherent | ||
| Organism: | Homo sapiens | ||
| Morphology: | polygonal |
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| Source: | Organ: skin Disease: malignant melanoma Derived from metastatic site: skin of thigh |
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| 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 cells are distributed for research purposes only. The Memorial Sloan-Kettering Cancer Center releases the line subject to the following: 1.) The cells or their products must not be distributed to third parties. Commercial interests are the exclusive property of Memorial Sloan-Kettering Cancer Center. 2.) Any proposed commercial use of these cells must first be negotiated with The Director, Office of Industrial Affairs, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; phone (212) 639-6181; FAX (212) 717-3439. | ||
| Tumorigenic: | Yes | ||
| Antigen Expression: | Blood Type A; Rh+ | ||
| Cytogenetic Analysis: | (P6) hypodiploid to hypertetraploid with abnormalities including dicentrics, secondary constrictions and large telocentric marker | ||
| Isoenzymes: | AK-1, 1 ES-D, 1 G6PD, B GLO-I, 2 PGM1, 1 PGM3, 1 |
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| Age: | 60 years | ||
| Gender: | male | ||
| Ethnicity: | Caucasian | ||
| Propagation: | ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%. |
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| Subculturing: | Protocol: Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended Medium Renewal: 2 to 3 times per week |
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| Preservation: | Freeze medium: Complete growth medium 95%; DMSO, 5% Storage temperature: liquid nitrogen vapor phase |
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| References: | 21869: . Human tumor cells in vitro. New York: Plenum Press; 1975. 22536: Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871 22539: Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080 32288: Landers JE, et al. Translational enhancement of mdm2 oncogene expression in human tumor cells containing a stabilized wild-type p53 protein. Cancer Res. 57: 3562-3568, 1997. PubMed: 9270029 |
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文献和实验1. Inoculate the entire colony in 5 ml YPD culture O.N. or 12 hours 2. Dilute into YPA medium (1% yeast extract, 2% Bacto-peptone, 2%KOAC) to OD600~ 0.2, Vigorous shaking. 3. For ts mutants, ~15hours at 23C, others ~10 hours at 30C
Induction of Erythroid-Specific Expression in Murine Erythroleukemia (MEL) Cell Lines
Murine erythroleukemia (MEL) cell lines are erythroid progenitor cells derived from the spleens of susceptible mice infected with the Friend virus complex 1 . These virally transformed cells are arrested at the proerythroblast stage
适用标准:GB/T3536-91(克力夫兰开口杯法)GB/T267-88 产品说明: 本仪器采用当代先进技术,集机械、光学,电子及计算机技术于一体,结构紧凑。可自动完成石油产品开口闪点的测试,实验过程中的升温速率及扫描点火动作由微机控制自动进行,油气闪火时,检测系统自动捕捉并记录闪点温度。对闪点数据进行自动气压修正,并以规范的格式打印输出,还可根据需要重复打印数据。 本仪器可由计算机监控(无线/有线通讯方式,由用户选配)。 本仪器结构合理,性能稳定,操作简单,是理想的分析
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