35 mm Glass bottom dish with 10 mm micro-well #1.5 cover glass
35mm glass bottom dish, dish size 35mm, well size 10mm, #1.5 glass(0.16-0.19mm). Designed for high resolution imaging such as confocal microscopy.
Note: We found that a small percentage of microscope adapters are too small for our 35 mm glass bottom dishes. Please check carefully the dimension diagram. If your adapter is too small, you should use our 29 mm glass bottom dish instead.
65 cases in stock
Features:
- Suitable for long term tissue culture
- Manufactured in a class 100,000 clean room
- Dish made from virgin polystyrene, tissue culture treated.
- German cover glass of superior optical quality
- A USP class VI adhesive is used to assemble the cover glass and the dish.
- Packed in easy to open peelable bag
- Sterilized by Gamma radiation.
Suitable for:
- Differential Interference Contrast (DIC)
- Widefield Fluorescence
- Confocal Microscopy
- Two-Photon and Multiphoton Microscopy
- Fluorescence Recovery After Photobleaching (FRAP)
- Förster Resonance Energy Transfer (FRET)
- Fluorescence Lifetime Imaging Microscopy (FLIM)
- Total Internal Reflection Fluorescence (TIRF)
- Super-Resolution Microscopy
Recommended for:
- Confocal Microscopy
Technical specifications
» View technical specification of different coverslips.
Coverslip | #1.5 cover glass (0.16 - 0.19 mm) |
---|---|
Temperature Range | -20°C to 50°C |
Lid diameter(outer) | 40 mm |
Dimension diagram (units in mm)
Cited Publications before 2019 (10)
-
The effect of low-intensity ultrasound and met signaling on cellular motility and morphology
N Mazzawi,, Applied Acoustics Volume 143, 1 January 2019, Pages 1-6
Quote: "The fluorescently tagged MDCK cells (pEYFP-mem & pmCherry) were seeded on a glass-coverslip bottomed 35 mm Petri dish (10 mm micro-well #1.5 cover glass, catalog number D35-10-1.5-N, Cellvis), 24 h before experiment" -
Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
Aidan M Fenix1, et al., ElifeScience, 2018
Quote: "For both live and fixed cell micros-copy, cells were plated and imaged on 35 mm glass bottom dishes with a 10 mm micro-well #1.5 cover glass (Cellvis, Mountain View, CA) coated with 25 mg/mL laminin (114956-81-9, Sigma-Aldrich)." -
Cell Polarity and Division Symmetry Analyses in Transformed Blood Cells
B Mizukawa, et al., Rho GTPases pp 257-266
Quote: "35 mm Glass-bottom dish (#1.5) with 10 mm diameter microwell (Cellvis D35-10-1.5-N)" -
In vitro exploration of ACAT contributions to lipid droplet formation during adipogenesis
Y Zhu, et al., Journal of Lipid Research, March 16, 2018
Quote: "Deuterium labeled glucose was used to visualize and quantify de novo lipogenesis by SRS imaging. 3T3-L1 preadipocytes were cultured in glass-bottomed dishes (#D35-10-1.5-N, Cellvis Inc.)." -
Visualizing Autophagic Lysosome Reformation in Cells Using In Vitro Reconstitution Systems
Yang Chen, et al., Current Protocols in Cell Biology 11.24.1–11.24.15, March 2018
Quote: "Amaxa Biosystems Nucleofector Device 3.5-cm glass-bottom dish (eg, In Vitro Scientific, cat. no. D35-10-1.5-N) 37°C, 5% CO2 incubator Confocal microscope with live-cell imaging system (eg, Olympus F1000) Visualizing Autophagic Lysosome Reformation" -
Force-activatable biosensor enables single platelet force mapping directly by fluorescence imaging
Y Wang, et al., Biosensors and Bioelectronics Volume 100, 15 February 2018, Pages 192-200 Biosensors and Bioelectronics
Quote: "In ITS surface preparation, glass-bottom dish (D35-10-1.5-N, In Vitro Scientific) or glass-bottom 96-well plate (P96G-0–5-F, MaTek Corp) was first immersed in 100 µg/ml BSA-biotin (biotinylated bovine serum albumin, A8549, Sigma-Aldrich) mixed with 5 µg/ml fibronectin for 30" -
Focal adhesion kinase regulates early steps of myofibrillogenesis in cardiomyocytes
Nilay Taneja, et al., bioRxiv, February 07, 2018.
Quote: "Cells were then resuspended in 200 μL of culture media and plated on 35 mm dishes with 10 mm glass bottom (D35-10-1.5-N; CellVis, Sunnydale, CA) pre-coated with 10 μg/mL fibronectin" -
Muscle specific stress fibers give rise to sarcomeres and are mechanistically distinct from stress fibers in non-muscle cells
Aidan M Feinx, et al., Biorxiv 2017
Quote: "cells were plated and imaged on 35 mm glass bottom dishes with a 10mm micro-well #1.5 cover glass (Cellvis, Mountain View, CA) coated with 25 μg/mL laminin" -
Highly sensitive transient absorption imaging of graphene and graphene oxide in living cells and circulating blood
Junjie Li, et al., Scientific Reports, June 2015
Quote: "cells were plated into 35 mm glass-bottom dishes (In Vitro Scientific, D35-10-1.5-N) at density of 1 × 10 5 cells/plate" -
Direct Visualization of De novo Lipogenesis in Single Living Cells
Junjie Li & Ji-Xin Cheng, Nature, Scientific Reports 4, October 29 2014
Quote: "For SRS imaging of glucose-d 7 , around 0.3 M cells were seeded on glass-bottom dishes (In Vitro Scientific, Cat# D35-10-1.5-N) with 25 mM glucose-d 7 in glucose-free DMEM media supplemented with or without 10% FBS"