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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 应用范围:
Cell Attachment;Cell Culture
- 宿主:
0
- 抗原来源:
0
- 库存:
大量
- 是否单克隆:
0
- 规格:
50
Product Images
- Cell Attachment
- Cell Culture
- Cell Differentiation
- Fluorescence
- Low Protein Binding
- Mouse Embryonic Stem Cells
- Human Embryonic Stem Cells
- Mesenchymal Stem Cells
- Neural Stem Cells
- Hematopoietic Stem Cells
- Epithelial Cells
- Pancreatic Stem Cells
- Cardiac Stem Cells
- Induced Pluripotent Stem Cells
- Embryonic Stem Cells
- Epithelial Cells
- Epithelial Stem Cells
- Mesenchymal Stem Cells
- Mouse Embryos
- Neonatal Liver Cells
- Neural Lineage Cells
- Primary Mouse Embryo Fibroblasts
- Endothelial Cells
Product Family Information
MultiScreen Plates and Millicell inserts with Teflon MembranesTeflon membranes have low reactivity, low protein binding and are extremely resistant to solvents and harsh chemicals. Fluoropore is available in filter plates and Biopore is available in Millicell inserts for cell-based assasy. |
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Millicell Cell Culture InsertsMillicell inserts are available for 24-, 12-, or 6-well plates. The inserts are easily prepared for SEM and TEM visualizing techniques, and they are compatible with cellular and/or fluorescent stains. |
更多产品技术资讯,请访问密理博中国博客:http://blog.milliporechina.com
详细描述见链接:http://www.millipore.com/catalogue/item/PICM03050
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文献和实验利用 Millicell 培养小室培养皮肤及肺类器官的实验方案
DMEM/F12) 混合均匀。避免在胶原蛋白中产生气泡。 c.加入400µl PHFs (4 × 106细胞/mL细胞悬液)或NIH 3T3细胞。完全混合,但避免产生胶原蛋白泡沫。本步骤在冰上进行。 d.将400µL的胶原蛋白/PHF混合物直接等分加入到每个MilliCell插入式细胞培养小室(MCHT12H48)的中心。 在加入时避免产生泡沫。将细胞培养小室/皿在37°C孵育至少30分钟便于完全聚合。在凝胶化后,胶原蛋白/PHF层在37°C的条件下不添加任何培养基,可保持使用长达5小时
containment level Centrifuge CO2 Incubator set at 37oC Microscope (uv Epi-Fluorescent.) 35mm plastic tissue culture dishes (Prod. No. C6296) Multidish 24 well (Prod. No. M9655) Cell scraper Microscope slides and 22mm cover slips Aluminum foil
Cell Suspension Culture of Arabidopsis
(either with or without light). After 7 to 10 days, the flask can be subcultured. 9. To subculture the cells, decant all of the liquid off and add 50 ml of fresh MSA. Pour the entire culture into a 250 ml flask. 10. When the volume of tissue has doubled, transfer 30
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