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- VivaCell
- C3132-0500
- 2026年01月19日
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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， without HEPES
- 规格：
500ml
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.
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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文献和实验基的离心管中，轻轻震荡混匀后，放置于 37℃ 培养箱中解离 1 h。每隔15min 轻轻震荡或吹打混匀一次。 5、加入 8ml 预冷的 DMEM/F12（含 10%FBS）终止消化。 6、将悬浮液经过 70μm 细胞筛网过滤，收集解离的细胞。 7、将过滤的细胞悬液在 4℃ 条件下 450g 离心 5min。 8、若细胞沉淀有明显的红色，则将细胞重悬于 5ml 的红细胞裂解液中，冰上孵育 10min 使红细胞裂解。 9、向细胞悬液中加入 5ml DMEM/F12 冲洗细胞一次，离心收集细胞沉淀后，加入
，促进解离。 4、向悬浮液中加入 50μl 脱氧核糖核酸酶（2mg / ml），并在 20°C-22°C 下孵育1min。 5、加入 8ml 预冷的 DMEM/F12（含 10%FBS）终止消化。 6、将悬浮液经过 70μm 细胞筛网过滤，收集解离的细胞。 7、将过滤的细胞悬液在 4℃ 条件下 220g 离心 5min。 8、用 1mlDMEM / F12（20°C-22°C）冲洗细胞一次，离心收集细胞沉淀后，加入500μl DMEM / F12（20°C-22°C）重悬细胞，并在细胞计数后，将细胞
基 NP培养基 中胚层诱导培养基 ABC3R培养基 C1F培养基 基础培养基 Knockout DMEM DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 DMEM/F12 Penicillin-Streptomycin
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