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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
UM-SCC-22B Squamous Carcinoma Cell Line
- 规格:
T25/冻存管
细胞名称:UM-SCC-22B Squamous Carcinoma Cell Line
货号:SCC077
种属:human
细胞系描述:Cancer Cells
应用:This product is available for sale to academic institutions or not-for-profit entities for research use.
质量:
• Each vial contains ≥ 1X10^6 viable cells.
• Cells are tested by PCR and are negative for HPV-16, HPV-18, Hepatitis A, B, C and HIV-1 & 2 viruses.
• Cells are negative for mycoplasma contamination.
• Each lot of cells are genotyped by STR analysis to verify the unique identity of the cell line.
储存及稳定性:UM-SCC-22B cells should be stored in liquid nitrogen. The cells can be cultured for at least 10 passages after initial thawing without significantly affecting the cell marker expression and functionality.
其他说明:Concentration: Please refer to lot specific datasheet.
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文献和实验Brenner JC, Graham MP, Kumar B, Saunders LM, Kupfer R, Lyons RH, Bradford CR, Carey TE. Genotyping of 73 UM-SCC head and neck squamous cell carcinoma cell lines. Head Neck. 2010 Apr;32(4):417-26. doi: 10.1002/hed.21198. PMID: 19760794; PMCID: PMC3292176.
Zhu Z, Xu X, Yu Y, Graham M, Prince ME, Carey TE, Sun D. Silencing heat shock protein 27 decreases metastatic behavior of human head and neck squamous cell cancer cells in vitro. Mol Pharm. 2010 Aug 2;7(4):1283-90. doi: 10.1021/mp100073s. PMID: 20540527; PMCID: PMC2914182.
Isolation and Culture of Squamous Cell Carcinoma Lines
Cutaneous squamous cell carcinoma (SCC) keratinocytes readily grow, expand in culture, and continuously passage, suggesting either spontaneous immortalisation at the early stage of culture or inherent proliferative capacity. One feature
Epigenome and DNA Methylation in Oral Squamous Cell Carcinoma
in epigenetic changes includes the posttranslational modifications of histones, mainly phosphorylation, deacetylation changes, and in the ubiquitinylation status. Oral squamous cell carcinoma is the most common malignancy of the oral cavity, and epigenetic
Cancer Stem Cells in Head and Neck Squamous Cell Carcinoma
isolated based on the presence of specific cell surface antigens. In head and neck squamous cell carcinomas, we have shown that the CSCs are contained within the CD44+ subset of tumor cells. This subset contains cells capable of initiating tumor growth










