Webinars

Designing the Future with Novel Stem Cell Culture

United Kingdom • Webinar

26 Feb 2025

Designing the Future: Novel Stem Cell Culture and RNA Tech

Singapore • Webinar

Complete camera overview of EM grid recorded with 3 channels. Inserts displaying the positions, where superresolved 3D confocal images were recorded. 3D renderings of these positions are shown in the zoomed inserts. Fluorescence channels (nuclei by Hoechst, blue; mitochondria by MitoTracker Green, green; lipid Droplets by Bodipy and Crimson Beads, red). Width of a grid square is 90 ?m, width of a grid bar is 35 ?m. Samples kindly provided by Ievgeniia Zagoriy, Mahamid-Group, EMBL Heidelberg, Germany.

From Bench to Beam: A Complete Correlative Cryo Light Microscopy Workflow

In the webinar entitled "A Multimodal Vitreous Crusade, a Cryo Correlative Workflow from Bench to Beam" a team of experts discusses the exciting world of correlative workflows for structural biology…

Transfection using the Uncommon Bio reprogramming system. Image acquired using the THUNDER Imager 3D Cell Culture with THUNDER Large Volume Computational Clearing (LVCC) applied. Image courtesy of Samuel East, Uncommon Bio.

Designing the Future with Stem Cell and RNA Technology

Visionary biotech start-up Uncommon Bio is tackling one of the world’s biggest health challenges: food sustainability. In this webinar, Stem Cell Scientist Samuel East will show how they use RNA…

Developing embryos of different species at different stages during the elongation of their posterior body axis, from left to right in developmental time. The labelled regions in red depict a region of undifferentiated cells called the tailbud, with the corresponding region generated from that tissue shaded in grey. Upper row: lamprey; middle row: catshark; bottom row, zebrafish. This figure has been adapted from the following publication: Steventon, B., Duarte, F., Lagadec, R., Mazan, S., Nicolas, J.-F., & Hirsinger, E. (2016). Species tailoured contribution of volumetric growth and tissue convergence to posterior body elongation in vertebrates. Development, 2016. 143(10):1732-41

How to Study Gene Regulatory Networks in Embryonic Development

Join Dr. Andrea Boni by attending this on-demand webinar to explore how light-sheet microscopy revolutionizes developmental biology. This advanced imaging technique allows for high-speed, volumetric…

[Translate to chinese:] GLP-1 and PYY localized to distinct secretory pools in L-cells.

前沿成像技术用于 GPCR 信号传导

通过这个按需网络研讨会，提升您的药理研究，了解 GPCR 信号传导，并探索旨在理解 GPCR 信号如何转化为细胞和生理反应的尖端成像技术。发现领先的研究，扩展我们对这些关键通路的认识，以寻找新的药物发现途径。

Stripe assay performed on a THUNDER Imager Cell. Courtesy of Maria Carrasquero Ordaz, University of Oxford.

Revealing Neuronal Migration’s Molecular Secrets

Different approaches can be used to investigate neuronal migration to their niche in the developing brain. In this webinar, experts from The University of Oxford present the microscopy tools and…

Dapi – Nucleus, GFP – Plasma Membrane, Thickness 100µm, 63x objektive, 469 Z planes, 2 channels, THUNDER Imager 3D Cell Culture. Courtesy M.Sc. Dana Krauß, Medical University of Vienna (Austria).

您的 3D 类器官成像和分析工作流程效率如何？

类器官模型已经改变了生命科学研究，但优化图像分析协议仍然是一个关键挑战。本次网络研讨会探讨了类器官研究的简化工作流程，首先是实时的三维细胞培养检查，接下来是高速、高分辨率的三维成像，生成清晰的图像和更纯净的数据，以便对生长速率、细胞迁移和三维细胞相互作用等参数进行准确地人工智能分割和量化，从而实现更深入的洞察。

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