29 mm Glass bottom dishes
Designed for high resolution imaging such as confocal microscopy.
We found that a small percentage of microscope adapters are too small for our 35 mm glass bottom dishes. 29 mm glass bottom dishes are designed for these adapters. In general 29 mm glass bottom dishes can fit into adapters that 35 mm glass bottom dishes fit. However 29 mm glass bottom dishes are smaller thus are harder to handle.
|Product #||Well Size||Coverslip » view coverslip spec||Packing||Price(case)|
|D29-10-0-N||10.0 mm||#0||10/sleeve, 100/case||$110.00|
|D29-10-1-N||10.0 mm||#1||10/sleeve, 100/case||$110.00|
|D29-10-1.5-N||10.0 mm||#1.5||10/sleeve, 100/case||$110.00|
|D29-14-0-N||14.0 mm||#0||10/sleeve, 100/case||$110.00|
|D29-14-1-N||14.0 mm||#1||10/sleeve, 100/case||$110.00|
|D29-14-1.5-N||14.0 mm||#1.5||10/sleeve, 100/case||$110.00|
|D29-20-0-N||20.0 mm||#0||10/sleeve, 100/case||$137.00|
|D29-20-1-N||20.0 mm||#1||10/sleeve, 100/case||$137.00|
|D29-20-1.5-N||20.0 mm||#1.5||10/sleeve, 100/case||$137.00|
|D29-20-1.5H||20.0 mm||#1.5H||10/sleeve, 100/case||$215.00|
|D29-20-1.5P||20.0 mm||#1.5P||10/sleeve, 100/case||$150.00|
- 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 or glass-like cover slip 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.
Cited publications (34)
The effect of substrate bulk stiffness on focal and fibrillar adhesion formation in human abdominal aortic endothelial cells
H Hassanisaber, et al., Materials Science and Engineering: C Available online 29 December 2018
Quote: "Prior to imaging, the samples were washed three times with 1× PBS and mounted on 29 mm glass-bottom petri-dishes (Cellvis, D29-20-0-N, California, USA) on 100 μl of 50% (v/v) Glycerol (Thermo Fisher Scientific, G33) in 1× PBS"
Vertebrate Dynein-f depends on Wdr78 for axonemal localization and is essential for ciliary beat
Y Zhang, et al., Journal of Molecular Cell Biology, 28 July 2018
Quote: "The remaining radial glia-enriched cells were further cultured to ∼80% con- fluency (usually 3 days) and then transferred into the wells of laminin-coated 29-mm glass-bottom dishes (Cellvis, D29-14-1.5-N) at a density of 2 × 10 5 cells per well (SS d–3)"
Mother centrioles are dispensable for deuterosome formation and function during basal body amplification
H Zhao, et al., BioRxiv, July 20, 2018
Quote: "The cells were then transferred into the wells of laminin-coated 29-mm glass-bottom dishes (Cellvis, D29-14-1.5-N) at a density of 2×105 cells per well and were maintained in serum-free medium to induce multiciliate mEPCs"
Non-canonical Opioid Signaling Inhibits Itch Transmission in the Spinal Cord of Mice
Admire Munanairi, et al., Cell Reports, Volume 23, Issue 3, 17 April 2018, Pages 866-877
Quote: "PKC Translocation Assay: KOR-GRPR HEK293 cells, transiently expressing PKCδ-EGFP or PKCα-EGFP (kindly provided by Dr. Peter M. Blumbergtaken) were seeded in 29-mm glass bottom dishes (In Vitro Scientific)."
ADAMTS9-Regulated Pericellular Matrix Dynamics Governs Focal Adhesion-Dependent Smooth Muscle Differentiation
Timothy J. Mead, et al., Cell Reports, Volume 23, Issue 2, 10 April 2018
Quote: "Monolayers of HUSMCs were grown and siRNA-transfected. The cells were re-plated on a glass-bottom dish (D-29-10-0-N; Cellvis, Mountain View, CA) and imaged 24 hr later in a heat/CO2-controlled environmental chamber on an inverted Leica SP8 confocal microscope"
Microtubule-bundling protein Spef1 enables mammalian ciliary central apparatus formation
J Zheng, et al., Journal of Molecular Cell Biology (2018), 1–11
Quote: "The remaining radial glia-enriched cells were further cultured to ∼90% confluency (usually 4 days) and then transferred into the wells of laminin-coated 29-mm glass-bottom dishes (Cellvis, D29-14-1.5-N) at a density of 2 × 10 5 cells per well"
In Vivo Superresolution Imaging of Neuronal Structure in the Mouse Brain
BE Urban, et al., IEEE Transactions on Biomedical Engineering ( Volume: 65 , Issue: 1 , Jan. 2018 )
Quote: "Before the solution solidified, 1 mL of the mixture was placed in a 29 mm glass bottom dish with a 20 mm bottom well (D29-20-0-N, In Vitro Scientific) and immediately placed in a 4 °C environment to solidify"
In vivo super-resolution imaging of neuronal structure in the mouse brain
BE Urban, et al., IEEE Transactions on Biomedic, Volume: 65 Issue: 1
Quote: "1 mL of the mixture was placed in a 29 mm glass bottom dish with a 20 mm bottom well (D29-20-0-N, In Vitro Scientific)"
Effect of pH on polyethylene glycol (PEG)-induced silk microsphere formation for drug delivery
J Wu, et al., Materials Science and Engineering: C Volume 80, 1 November 2017, Pages 549-55
Quote: "Drug-loaded silk microspheres were suspended in 20 μl ultrapure water which was added to a well of cell culture dish with a glass bottom (29 mm dish with 20 mm bottom well, In Vitro Scientific"
Cellular Contraction Can Drive Rapid Epithelial Flows
Dhruv K.Vig, et al., Biophysical Journal, Volume 113, Issue 7, 3 October 2017, Pages 1613-1622
Quote: "silane (3-aminopropyl triethoxysilane) (Sigma-Aldrich) was vapor-deposited onto a 29-mm glass-bottom dish with a 14-mm microwell (In Vitro Scientific)"