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Key Documents

Z734853

Nunc ® Lab-Tek ® II 腔室盖玻片

8 wells, polystyrene chambers, 1.5 borosilicate coverglass, 0.7 cm2/well, 96/cs

别名:

chamber slides, microscope slides, microscopy slides

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About This Item

分類程式碼代碼:
41122600
NACRES:
NB.22

材料

borosilicate glass
colorless
polystyrene chamber

無菌

non-sterile
sterile

品質

CE marked

包裝

case of 96

製造商／商標名

Nunc 155409

寬度 × 長度

24 mm × 55 mm

孔面積

0.7 cm2

孔

8

有效容積

0.2-0.5 mL

適合性

suitable for (high power inverted microscopic viewing; confocal image analysis)

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一般說明

  • 非常适合共聚焦图像分析
  • 最适合高功率倒置显微镜观察
  • 腔室盖玻片
  • 培养液槽不可拆卸

特點和優勢

  • 在单个设备上培养、检查和分析活细胞的理想选择。
  • 可提供 1、2、4 和 8 孔形式。
  • 采用生物相容性丙烯酸粘合剂将培养基腔室安全地固定在 1.5 号硼硅酸盐盖玻片上。
  • 带标签的聚苯乙烯盖实现最小的蒸发量，确保最佳的气体交换。
  • 在可堆叠的培养托盘中方便地运输。

法律資訊

Lab-Tek is a registered trademark of Thermo Fisher Scientific or its subsidiaries
Nunc is a registered trademark of Thermo Fisher Scientific or its subsidiaries

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Massimo D'Agostino et al.
The EMBO journal, 37(19) (2018-08-19)
Constitutive membrane fusion within eukaryotic cells is thought to be controlled at its initial steps, membrane tethering and SNARE complex assembly, and to rapidly proceed from there to full fusion. Although theory predicts that fusion pore expansion faces a major
Charles R Krois et al.
Cellular and molecular life sciences : CMLS, 76(12), 2425-2447 (2019-02-23)
RDH1 is one of the several enzymes that catalyze the first of the two reactions to convert retinol into all-trans-retinoic acid (atRA). Here, we show that Rdh1-null mice fed a low-fat diet gain more weight as adiposity (17% males, 13%
Mary Mirvis et al.
PLoS biology, 17(7), e3000381-e3000381 (2019-07-18)
The primary cilium is a central signaling hub in cell proliferation and differentiation and is built and disassembled every cell cycle in many animal cells. Disassembly is critically important, as misregulation or delay of cilia loss leads to cell cycle
Dae-Hee Lee et al.
Autophagy, 14(11), 1870-1885 (2018-07-07)
Macroautophagy is induced under various stresses to remove cytotoxic materials, including misfolded proteins and their aggregates. These protein cargoes are collected by specific autophagic receptors such as SQSTM1/p62 (sequestosome 1) and delivered to phagophores for lysosomal degradation. To date, little

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