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Z688835

Nunc® UpCell表面细胞培养皿

别名:

cell culture dish, tissue culture dish

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30 EA
$2,420.00

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30 EA
$2,420.00

About This Item

分類程式碼代碼:
41121812
NACRES:
NB.22

$2,420.00


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材料

polystyrene

無菌

sterile

特點

lid vented
membrane not included

包裝

case of 30 ea

製造商/商標名

Nunc 174903

皿直徑× 高度

60 mm × 15 mm

外部長度 × 寬度

60 mm × 15 mm

尺寸

60 mm

表面積

21.5 cm2 , culture area (cm2)/well

有效容積

5 mL

結合類型

(UpCell Surface)

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一般說明

Nunc UpCell 表面培养皿具有温度响应型细胞培养表面。这些 UpCell 表面培养皿适用于收获具有完整表面蛋白的细胞,用于培养传代、单细胞分析和细胞移植研究。UpCell 表面能够收集细胞层并通过正常细胞连接和细胞外基质将这些细胞连接起来而创建三维组织模型。


  • 收集具有完整表面蛋白的细胞
  • 不进行胰蛋白酶消化 - 保留细胞表面蛋白
  • 无需机械力处理 - 获得高细胞活性
  • 通过降低细胞培养物的温度释放贴壁细胞
  • 用于培养传代、单细胞分析和细胞移植研究
  • 能收集细胞层并通过正常细胞连接和细胞外基质将这些细胞连接起来而创建三维组织模型
  • 最少的动手操作时间
  • 仅供研究和一次性使用
  • 快速、清洁、简单 - 只需降低温度

注意:适用于收集具有完整表面蛋白的细胞,用于细胞培养传代、单细胞分析和细胞移植研究

法律資訊

Nunc is a registered trademark of Thermo Fisher Scientific or its subsidiaries
UpCell is a trademark of Thermo Fisher Scientific or its subsidiaries

历史批次信息供参考:

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Questions

  1. How many minutes does it take to Detach cells at 20 degree from 100 mm dish?  Does cells be released as a single cells ? Or sheet format?  Your answer is appreciated. Thanks 

    1 answer
    1. This is a product Nunc/ThermoFisher. The manufacturer offers the same detachment information, regardless of dish size or number of wells.
      The following example protocol for cell suspensions:
      1. Mouse Peritoneal Macrophages were washed with Ca2+– and Mg2+–free PBS to remove non-adherant cells
      2. Fresh medium including FBS was added to the plate.
      3. Cultures were incubated for 30 minutes at 20°C prior to harvesting.

      The following example protocol for harvesting cells as a single sheet:
      Madin-Darby Canine Kidney (MDCK) cells in Dulbecco’s Modifi ed Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS), penicillin (100 units/mL) and streptomycin (100 μg/mL) were seeded at 5.7 x 104 cell/cm2 in a 3.5 cm dish with UpCell Surface. The cells were incubated for 21 days at 37°C in a humidifi ed atmosphere of 5% CO2 in air. The cells were then harvested as an intact sheet:
      1. The dish was placed at 20°C for 60 min.
      2. A supporting membrane was placed on top of the cell layer and the culture medium was aspirated
      3. The edge of the membrane was gently released from the dish using forceps, and the membrane with the attached cell layer was then transferred to a cell culture insert and incubated at 20°C for 30 min.
      4. Sufficient culture medium was added to cover the cell sheet and membrane and the membrane was removed from the cell layer using forceps

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