STELLARIS 8 FALCON 蛍光寿命イメージングを素早く入手



In vivo imaging of a mouse pial and cortical vasculature through a glass window (ROSAmT/mG::Pdgfb-CreERT2 mouse meningeal and cortical visualization following tamoxifen induction and craniotomy). Courtesy: Thomas Mathivet, PhD

Windows on Neurovascular Pathologies

Discover how innate immunity can sustain deleterious effects following neurovascular pathologies and the technological developments enabling longitudinal studies into these events.
Lifetime-based multiplexing in live cells using TauSeparation. Mammalian cells expressing LifeAct-GFP (ibidi GmbH) and labelled with MitoTracker Green. Acquisition with one detector, intensity information shown in grey. The two markers can be separated using lifetime information: LifeAct-GFP (cyan), MitoTracker Green (magenta). Image acquired with STELLARIS 5.

The Power of Reproducibility, Collaboration and New Imaging Technologies

In this webinar you willl learn what impacts reproducibility in microscopy, what resources and initiatives there are to improve education and rigor and reproducibility in microscopy and how…
Combining spectrally resolved detection and fluorescence lifetime multiplexing

Live-Cell Fluorescence Lifetime Multiplexing Using Organic Fluorophores

On-demand video: Imaging more subcellular targets by using fluorescence lifetime multiplexing combined with spectrally resolved detection.
Donor (D) and acceptor (A) molecule which participate in FRET (Förster resonance energy transfer).

What is FRET with FLIM (FLIM-FRET)?

This article explains the FLIM-FRET method which combines resonance energy transfer and fluorescence lifetime imaging to study protein-protein interactions.

Visualizing Protein-Protein Interactions by Non-Fitting and Easy FRET-FLIM Approaches

The Webinar with Dr. Sergi Padilla-Parra is about visualizing protein-protein interaction. He gives insight into non-fitting and easy FRET-FLIM approaches.
Transverse histological cut of a rabbit tongue. 50 Mpixels images (2326 µm x 1739 µm) in 14 x 18 tiles. Lifetime gives an additional contrast that allows to differentiate different structures in histological stainings.

A Guide to Fluorescence Lifetime Imaging Microscopy (FLIM)

The fluorescence lifetime is a measure of how long a fluorophore remains on average in its excited state before returning to the ground state by emitting a fluorescence photon.
Identification of distinct structures_roundworm_Ascaris_female

Find Relevant Specimen Details from Overviews

Switch from searching image by image to seeing the full overview of samples quickly and identifying the important specimen details instantly with confocal microscopy. Use that knowledge to set up…

How to Quantify Changes in the Metabolic Status of Single Cells

Metabolic imaging based on fluorescence lifetime provides insights into the metabolic dynamics of cells, but its use has been limited as expertise in advanced microscopy techniques was needed. Now,…

How FLIM Microscopy Helps to Detect Microplastic Pollution

The use of autofluorescence in biological samples is a widely used method to gain detailed knowledge about systems or organisms. This property is not only found in biological systems, but also…


LIGHTNINGは、他の方法では簡単に可視化できない、微細な構造や形態を完全自動で明らかにする、適応能力に優れた情報抽出プロセスです。 LIGHTNINGは、画像全体を同一のパラメーターで演算する従来型の手法とは異なり、ボクセル(3次元画素)ごとに適切なパラメーターを算出することによって、最高の忠実度であらゆる微細形態を明らかにします。

Microscopy in Virology

The coronavirus SARS-CoV-2, causing the Covid-19 disease effects our world in all aspects. Research to find immunization and treatment methods, in other words to fight this virus, gained highest…

TauSense Technology Imaging Tools

Leica Microsystems’ TauSense technology is a set of imaging modes based on fluorescence lifetime. Found at the core of the STELLARIS confocal platform, it will revolutionize your imaging experiments.…



蛍光寿命イメージング顕微鏡法(FLIM)は、蛍光色素固有の特性を活かしたイメージング技術です。 各蛍光分子は、固有の蛍光スペクトルに加えて、蛍光体が光子放出前に励起状態に留まる時間を反映する固有の寿命を持っています。 寿命解析により、標準的な蛍光強度測定に加え、新たな情報を得ることができます。


視点を単体の顕微鏡コンポーネントから必要なすべての機能を備えた生細胞イメージングソリューションへと移し、ライカ マイクロシステムズは顕微鏡、LAS X イメージングソフトウェア、カメラおよび専用サードパーティコンポーネントを 1 つの完全な生細胞イメージングシステムに統合します。


ライフサイエンス研究で近年最も目覚ましい発展の一つは、オルガノイド、スフェロイド、生体機能チップモデルなどの3D細胞培養システムの開発です。 3D細胞培養は、細胞が成長し、全3次元で周囲と相互作用できる人工環境です。 これらの条件は、生体内条件に似ています。




高度な顕微鏡技術には、高解像度および超解像のイメージング技術が含まれます。これらの技術は主に、細胞や組織などの試料にできるだけ優しく、極めて高い解像度で生物学的事象を可視化するために使用されます。 研究者は、高度な顕微鏡技術によって、生物学的経路、遺伝子やタンパク質の発現、病気のメカニズムなどに大きな影響を与える生体分子を調べ、理解することができます。
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