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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 供应商:
上海逍鹏生物科技有限公司
- 库存:
充足
- 英文名:
DMEM/F12 1:1 mixture, with L-Glutamine and HEPES
- 规格:
500ml
【Product Description】
Dulbecco's Modified Eagle Medium /Nutrient Mixture F12 Ham(DMEM/F12 1:1 mixture) with L-Glutamine and HEPES was originally formulated for rat neuroblastoma cells and MDCK cells. The mixture is extremely nutritious and supports growth of a wide variety of cells including certain epithelial, endothelial and granulosa cells.
It does not contain trace elements. Users are advised to review the literature for recommendations regarding medium supplementation and physiological lines.
【Storage and Stability】
Dulbecco's Modified Eagle Medium /Nutrient Mixture F12 Ham(DMEM/F12 1:1 mixture) with L-Glutamine and HEPES should be kept 2-8°C. The product is light -sensitive and therefore should not be left in the light. When stored in the dark under ideal conditions, the product is stable until the expiry date.
As with any other liquid media formulations, deterioration of liquid media may be recognized by any of the following characteristics, among others including:
(a). Color Change;
(b). Presence of clumping/flocculent debris/ granulation/ particulates\ precipitates or sediments;
(c). Insolubility;
(d). And/or decrease in expected performance parameters.
Any material described above should not be used and therefore discarded.
【Procedure】
1.Take a bottle from the defined storage conditions at 2-8°C and read the label.
2.Wipe the outside of the bottle with a disinfectant solution such as 70% ethanol.
3.Using aseptic/sterile technique under a laminar-flow culture hood, work according to established protocols.
4.Antibiotics may be added if desired.
【Quality Control】
Dulbecco's Modified Eagle Medium /Nutrient Mixture F12 Ham(DMEM/F12 1:1 mixture) with L-Glutamine and HEPES is tested for sterility, pH, osmolality and endotoxin concentrations. In addition, each batch is tested for cell growth using A549.
【Precaution and Disclaimer】
For research use only, not for clinical diagnosis and treatment.
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文献和实验,补充以2mm谷氨酰胺,6mg/ml葡萄糖,1mg/ml谷胱甘肽,10 units/ml青霉素,10ul/ml链霉素和7.5%胎牛血清)。细胞然后种植于35mm的预先以10ug/m1 po1y1ysine (Sigma)和2.5ug/ml merosin(Chemicon)铺底的培养皿中,种植密度为50,000细胞/cm2。培养16小时后,培养基换为无血清培养基。该培养基为F12和basa1Eag1e’s medium,补充以33mM葡萄糖,2mM谷氨酰胺, 15 mM碳酸氢钠,10mM HEPES
实验材料: 1. 一般来自鼻咽癌活检组织或引产胚胎的鼻咽组织; 2. 不含Ca2+ 和Mg2+ 的1×PBS,添加200000IU/L青霉素、200mg/L链霉素,pH7.2; 3. 培养基:可使用ROMI1640培养液,添加20%胎牛血清、5μg/ml胰岛素、2.7×10-7 mol/L氢化可的松。也可用DMEM培养液; 4. 低血清培养液与无血清培养液:基础培养液均为DMEM/F12(1:1,V/V)混合液。配置时,添加1.2g/L
一、常规的试剂配制: 1、培养基:选用高糖型DMEM/F12 (1:1)培养基干粉(含15 mmol Hepes),每升培养液中加入碳酸氢钠1.8 g,调节pH值7.0,0.22 μm的微孔滤膜过滤除菌后,加入谷氨酰胺、无菌的青霉素和链霉素液,使其终浓度分别为0.5 mmol/L 、100 U/ml和100 μg /ml,分装后置于4℃保存,临用前加入2%的B27。神经细胞代谢旺盛,选用高糖型培养基;谷胱甘肽可保持培养
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