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Publications Citing Cellvis (formerly In Vitro Scientific) Products

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Publications citing Cellvis "29 mm Glass bottom dishes"

1 - 34 of 34 publications before 2019

  1. 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"

  2. 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)"

  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"

  4. 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)."

  5. 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"

  6. 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"

  7. 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"

  8. 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)"

  9. 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"

  10. 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)"

  11. Patterned surface anchoring of nematic droplets at miscible liquid–liquid interfaces
    X Wang, et al., Soft Matter, 2017
    Quote: "29 mm-in-diameter glass bottom dish with 10 mm-in-diameter and 1 mm-in-depth microwell (#1.5 cover glass) was purchased from Cellvis (Mountain View, CA)"

  12. Subdiffractional tracking of internalized molecules reveals heterogeneous motion states of synaptic vesicles
    erja Joensuu, et al., The Journal of Cell Biology
    Quote: "Hippocampal neurons were obtained from Sprague Dawley rats at embryonic day 18 as previously described (Kaech and Banker, 2006; Heine et al., 2008; Harper et al., 2011) and cultured on poly-d-lysine–coated glass-bottom dishes (D29-20-1.5N; Cellvis)"

  13. The machinery underlying malaria parasite virulence is conserved between rodent and human malaria parasites
    Mariana De Niz, et al., Nature Communications
    Quote: "For binding assays, individual CHO cell lines were grown to 70% confluence, and 104 cells seeded in 33 mm polystyrene dishes (In Vitro Scientific) 24–36 h before binding assays"

  14. Structural insights and in vitro reconstitution of membrane targeting and activation of human PI4KB by the ACBD3 protein
    M Klima, et al., Sci Rep. 2016; 6: 23641.
    Quote: "COS-7 cells were plated onto 29-mm-diameter poly-L-Lysine coated glass bottom dishes (In Vitro Scientific) at 100,000 cells/well density and transfected using the Lipofectamine2000 reagent"

  15. The ML1Nx2 Phosphatidylinositol 3, 5-Bisphosphate Probe Shows Poor Selectivity in Cells
    GRV Hammond, et al, PLOS One, October 13, 2015
    Quote: "Cells seeded in 29 mm glass bottom dishes (CellVis) were transfected"

  16. Mitochondria-acting hexokinase II peptides carried by short-length carbon nanotubes with increased cellular uptake, endosomal evasion, and enhanced bioactivity
    Sia Lee Yoong, et al., Nanoscale, July 2015
    Quote: "MCF-7 cells were seeded into a 29 mm glass bottom dish (In Vitro Scientific, USA) at a density of 5 × 10 4 cells per mL for 24 h"

  17. Control of Autophagosome Axonal Retrograde Flux by Presynaptic Activity Unveiled Using Botulinum Neurotoxin Type A
    Tong Wang, et al., The Journal of Neuroscience, 15 April 2015, 35(15): 6179-6194
    Quote: "devices were design based on aforementioned devices but adapted to fit on 22 mm, glass-bottomed, super-resolution compatible culture dish dishes (In Vitro Scientific, catalog #D29-20-1.5-N)"

  18. Spatiotemporal Stability of Neonatal Rat Cardiomyocyte Monolayers Spontaneous Activity Is Dependent on the Culture Substrate
    J Boudreau-Béland, et al., Plos One, Jan 2, 2015
    Quote: "Isolated cells (enriched cardiomyocytes) were counted and seeded at a density of 10 6 cells/mL in 20-mm diameter glass-bottom culture dishes (D29-20-0-N, In Vitro Scientific, Sunnyvale, CA, USA) pre-coated (on glass or on PDMS)"

  19. Tropomyosin isoforms support actomyosin biogenesis to generate contractile tension at the epithelial zonula adherens
    Benjamin J. Caldwell, et al., Cytoskeleton, 2014
    Quote: "For transient transfection of plasmids, Caco-2 monolayers were seeded at 40% confluency on either 29mm glass bottom dish (In Vitro Scientific) for live cell imaging analysis"

  20. Multicellular automaticity of cardiac cell monolayers: effects of density and spatial distribution of pacemaker cells
    JE Duverger, et al., New Journal of Physics, Volume 16, November 2014
    Quote: "Isolated cells (enriched cardiomyocytes) were counted and seeded at a density of 1 × 10 6 cells mL −1 in 29 mm diameter glass-bottom culture dishes (D29-20-0-N, In vitro Scientific, Sunnyvale, CA) pre-coated with 0.2% gelatine and 0.001 25% fibronectin solution"

  21. A G-Protein Subunit Translocation Embedded Network Motif Underlies GPCR Regulation of Calcium Oscillations
    Lopamudra Giri, et al., Biophysical Journal, Volume 107, Issue 1, p242–254, 1 July 2014
    Quote: "0.2 × 10 6 cells were seeded on 29 mm glass bottom dishes (In Vitro Scientific, Sunnyvale, CA) and maintained in culture until 70–80% confluency."

  22. Subcellular optogenetic inhibition of G proteins generates signaling gradients and cell migration
    Patrick R. O’Neill et al., Mol. Biol. Cell June 11, 2014
    Quote: "Cells were plated at 2x10 5 cells per dish in 29 mm glass bottom dishes (In Vitro Scientific) one day prior to transfection"

  23. Optical control of protein activity and localization by fusion to photochromic protein domains
    X Zhou, MZ Lin, US Patent 2014
    Quote: "Hela cells were transfected at 75-90% confluency with Lipofectamine 2000 (Invitrogen) in 33-mm coverglass-bottom dishes (In Vitro Scientific)"

  24. “Pointsource” Delivery of a Photosensitizer Drug and Singlet Oxygen: Eradication of Glioma Cells In Vitro
    Ashwini A. Ghogare et al, Photochemistry and Photobiology, April 2014
    Quote: "Cell culture glass bottom dishes (29 mm glass well size and 14 mm microwell) and #1 cover glass (0.13–0.16 mm) were purchased from In Vitro Scientific (Sunnyvale, CA)"

  25. A novel probe for phosphatidylinositol 4-phosphate reveals multiple pools beyond the Golgi
    Gerald R.V. Hammond, et al., The Journal of Cell Biology, April 2014, Vol. 205 no. 1 113-126
    Quote: "Cells were seeded in 29-mm dishes with 20-mm #1 cover glass bottoms (In Vitro Scientific) at appropriate densities so that cells reached 50–100% confluence on the day of imaging"

  26. RGS2 regulates urotensin II‐induced intracellular Ca2+ elevation and contraction in glomerular mesangial cells
    Adebowale Adebiyi, Journal of Cellular Physiology, 2013
    Quote: "Intracellular Ca2+ [Ca2+]i imaging GMCs were seeded sparsely on 29 mm glass-bottom dishes with 14 mm micro-well (In Vitro Scientific, Sunnyvale CA)."

  27. Optically triggering spatiotemporally confined GPCR activity in a cell and programming neurite initiation and extensions
    W. K. Ajith Karunarathne, Lopamudra Giri, Vani Kalyanaraman, and N. Gautam, PNAS April 23, 2013, vol. 110 no. 17
    Quote: "A total of 0.1 × 106 cells were seeded in 29-mm glass-bottom dishes (In Vitro Scientific) the day before transfections"

  28. Identification of Endoplasmic Reticulum Export Motifs for G Protein-Coupled Receptors
    Guangyu Wu, Methods Enzymol. 2013; 521: 189–202.
    Quote: "COS7 cells are grown on 29-mm glass-bottom culture dishes (In Vitro Scientific) and transfected with either YS mutant"

  29. G-protein signaling leverages subunit-dependent membrane affinity to differentially control βγ translocation to intracellular membranes
    Patrick R. O’Neill, W. K. Ajith Karunarathne, Vani Kalyanaraman, John R. Silvius, and N. Gautam, Proc Natl Acad Sci U S A. 2012 December 18; 109(51): E3568–E3577.
    Quote: "Cells were cultured and transiently transfected in 29-mm glass-bottom culture dishes (In Vitro Scientific), using Lipofectamine 2000 (Invitrogen) and 1 μg of DNA corresponding to each transfected subunit"

  30. Assembly of Dishevelled 3-based supermolecular complexes via phosphorylation and Axin
    Noriko Yokoyama, Nelli G Markova, Hsien-yu Wang and Craig C Malbon, Journal of Molecular Signaling, 2012 7:8, doi:10.1186/1750-2187-7-8
    Quote: "COS7cells were cultured on 29 mm glass bottom culture dishes (In Vitro Scientific,Sunnyvale, CA) and transfected with GFP-tagged α2B-AR mutants"

  31. Visualizing Escherichia coli Sub-Cellular Structure Using Sparse Deconvolution Spatial Light Interference Tomography
    Mustafa Mir, S. Derin Babacan, Michael Bednarz, Minh N. Do, Ido Golding, Gabriel Popescu, Plosone, June 2012, Volume 7, issue 6
    Quote: "The cells are then concentrated to an OD of ~0.4 and 2 µl of the culture ispipetted onto a glass bottom dish (In Vitro Scientific D29-20-1-N) and covered bya 1 mm thick agar slab (1.5% Agarose, M9CA media)."

  32. All G protein βγ complexes are capable of translocation on receptor activation
    W.K. Ajith Karunarathne, Patrick R. O’Neill, Pedro L. Martinez-Espinosa, Vani Kalyanaraman, N. Gautam, Biochemical and Biophysical Research Communications, April 2012
    Quote: "Cells were cultured and transiently transfected either in 29 mm glassbottom culture dishes (In vitro Scientific) or on 40 mm glass coverslips"

  33. A Triple Arg Motif Mediates α2B-Adrenergic Receptor Interaction with Sec24C/D and Export
    Chunmin Dong, Charles D. Nichols, Jianhui Guo, Wei Huang, Nevin A. Lambert, Guangyu Wu, Traffic 2012, DOI: 10.1111/j.1600-0854.2012.01351.x
    Quote: "COS7 cells were cultured on 29 mm glass bottom culture dishes (In Vitro Scientific, Sunnyvale, CA) and transfected with GFP-tagged α2B-AR mutants"

  34. Analyzing planar cell polarity during zebrafish gastrulation.
    Jason R. Jessen, Methods in Molecular Biology, 2012, Volume 839, 69-78, DOI: 10.1007/978-1-61779-510-7_6
    Quote: "Glasspetri dishes for dechorionating live embryos. 7. 0.16–0.19 mm glass coverslip dishes(In Vitro Scientific, cat. no. D29-14-1.5-N or MatTek, cat. no"