Your Compact Confocal for Multiplex Imaging

高解析:提升2倍的解析度(逼近超高解析度SIM的解析能力)
低價格高規格的組合,客製化滿足不同的實驗需求
- Scan head 全新光路設計
精準的Pinhole位置,絕無色差問題,可連續調整針孔大小,進而達到精確的光學切片厚度。
FixGate main beamsplitter,操作方便,且採與LSM 980相同的低角度設計,高反射性的樣品也不會干擾影像擷取。
- LSM 900 延續 LSM 700的分光設計
精準的Pinhole位置,絕無色差問題,可連續調整針孔大小,進而達到精確的光學切片厚度。
FixGate main beamsplitter,操作方便,低角度設計,高反射性的樣品也不會干擾影像擷取。
- 實用的雷射模組
固態雷射具有體積小、穩定等優點,且壽命超長,省去日後需常更換的煩惱。]
- 經濟實惠的價格


螢光感測器可以選擇傳統光電倍增管(PMT)或是磷酸砷化鎵(GaAsP)感測器!

LSM900 同時支援Zeiss 推出最新技術Airyscan 2 ! ,XYZ解析度同步提升2倍的超高解析技術,488nm波長的激發下,XY可以解析到120nm,Z軸也有350nm的解析力!


LSM 900 with Airyscan 2 依照客戶需求可進行2Y(兩倍的速度)、4Y(四倍高速)下進行高解析影像擷取。

LSM 900 Neurons DepthCoded 3D, Fluorescence

The micrograph shows a Lilium auratum pollen grain, acquired with Airyscan 2 in Multiplex mode. Image courtesy of Jan Michels, Zoological Institute, Kiel University

LSM 900 Airyscan 2, Drosophila ZEN Connect 1-01-Airyscan Processing-01-Stitching-02-Color-coded Projection-04-2

Mouse brain slice; EGFP-Thy1 (green): nerve cells (subset), Calretin-Cy3 (red): Calretinin-expressing neurons,GAD65-Cy5 (blue): GABAergic synapses. Scale bar 50 µm.
Living Pig Kidney Epithelial cells (LLC-PK1), green: Tubulin-eGFP, red: h2b-mCherry; Imaged with ZEISS LSM 800 with Airyscan, Plan-Apochromat 63x/1.4 Oil,
Drosophila brain, neuromuscular junction stained for Bruchpilot (BRP), comparison between confocal LSM and Airyscan.
The example shows Kaede expressed in HepG2 cells before photoactivation (0 s) and at different time points (1 s, 3 s and 10 s) after repeated photoactivation (every 0.1 s) with 405 nm at the indicated regions (white box).
Kaede diffuses freely between the nucleus and the cytoplasm. The relative intensities in AU of the non-converted form (green bars) and converted form (red bars) are shown in each image.
Hep G2 cells, application image for FRET,Two interacting proteins (donor false coloredin green, acceptor false colored in red) in HepG2 cells ("before bleach"). By acceptor-photobleaching (within the indicated white circle) acceptor intensity will decrease while donor intensity will increase ("after bleach") as indicated by the green (donor)and red (acceptor) bars. The increase in donor intensity can be used to calculate FRET efficiencies.