傳統熒光顯微鏡受到光學衍射限的影響，高的分辨率為200 nm，因此很難觀察細胞中的超微結構。LiveCodim是一款模塊化超分辨共聚焦顯微系統，能夠適配絕大多數的倒置熒光顯微鏡，將現有的倒置顯微鏡升成為具備寬場、共聚焦、超分辨三大模式的成像系統。LiveCodim通過特的錐形衍射顯微鏡—— 一種強大的波束成形器，能夠直接提供分辨率高達120 nm的實時活細胞超分辨共聚焦成像，同時無需對樣品進行任何額外操作，結合其低光毒性，以及方便快捷的操作系統等優勢，非常適合拍攝熒光成像。
產品優勢
· 超高性價比：模塊化超分辨，節省成本，兼容絕大多數倒置顯微鏡
· xy軸超高分辨率：<120 nm
· z軸深度成像：具備z-stack成像能力，高成像深度50 μm
· 活細胞成像：低光毒性和光漂白性，適合活細胞成像
· 制樣簡單：樣品無需特殊處理，無需特殊染料
· 全自動軟件：全自動調節各種參數，簡單易上手
主要參數
· xy軸分辨率：< 120 nm
· z軸分辨率：< 500 nm
· z軸成像深度：50 μm
· 成像視野：共聚焦模式下80 μm * 80 μm，超分辨模式下： 50 μm * 50 μm
· 成像模式：寬場、共聚焦、LiveCodim超分辨
· 四色成像通道：405 nm, 488 nm, 561 nm, 640 nm (根據需求可增加)
測試數據
1. MDCK細胞中線粒體的動態變化
2. Hela胞的微管寬場，共聚焦，LiveCodim超分辨成像
3. 細胞分裂中期的COS-7細胞3D多色超分辨成像
4. 植物細胞成像：觀測鈴蘭草的根莖
5. 天然免疫分子TRIM5α作用機制研究
天然免疫分子TRIM5α蛋白是人類基因中決定疾病的易感性和發病速度的重要因素，其抗病毒活性通常通過小泛素相關修飾物(SUMO)調節，但是具體的作用機制仍有待進一步研究。LiveCodim超分辨圖像揭示了TRIM5α主要分布在肌小管的核膜上，同時與存在于核孔的細胞質絲上的RanGTPase蛋白RanGAP1有明顯的共定位現象，和主要定位于核籃上的蛋白Nup153無明顯共定位，說明TRIM5α主要定位于這類細胞的胞質面。
部分發表文章
[1] Fernandez, Juliette, et al. "Transportin-1 binds to the HIV-1 capsid via a nuclear localization signal and triggers uncoating." Nature microbiology 4.11 (2019): 1840-1850.
[2] Vargas, Jessica Y., et al. "The Wnt/Ca2+ pathway is involved in interneuronal communication mediated by tunneling nanotubes." The EMBO journal 38.23 (2019): e101230.
[3] Maarifi, Ghizlane, et al. "RanBP2 regulates the anti-retroviral activity of TRIM5α by SUMOylation at a predicted phosphorylated SUMOylation motif." Communications biology 1.1 (2018): 1-11.
[4] Garita-Hernandez, Marcela, et al. "Optogenetic light sensors in human retinal organoids." Frontiers in neuroscience 12 (2018): 789.
[5] Getz, Angela M., et al. "Tumor suppressor menin is required for subunit-specific nAChR α5 transcription and nAChR-dependent presynaptic facilitation in cultured mouse hippocampal neurons." Scientific reports 7.1 (2017): 1-16.
[6] Portilho, Débora M., Roger Persson, and Nathalie Arhel. "Role of non-motile microtubule-associated proteins in virus trafficking." Biomolecular concepts 7.5-6 (2016): 283-292.
[7] Pagliuso, Alessandro, et al. "A role for septin 2 in Drp1‐mediated mitochondrial fission." EMBO reports 17.6 (2016): 858-873.
[8] Fallet, Clement, and Gabriel Y. Sirat. "Achromatization of conical diffraction: application to the generation of a polychromatic optical vortex." Optics letters 41.4 (2016): 769-772.
[9] Fallet, Clement, et al. "Accurate axial localization by conical diffraction beam shaping generating a dark-helix PSF." Single Molecule Spectroscopy and Superresolution Imaging IX. Vol. 9714. International Society for Optics and Photonics, 2016.
[10] Fallet, Clement, Arvid Lindberg, and Gabriel Y. Sirat. "Generating 3D depletion distribution in an achromatic single-channel monolithic system." Single Molecule Spectroscopy and Superresolution Imaging IX. Vol. 9714. International Society for Optics and Photonics, 2016.
[11] Fallet, Clément, et al. "A new method to achieve tens of nm axial super-localization based on conical diffraction PSF shaping." Single Molecule Spectroscopy and Superresolution Imaging VIII. Vol. 9331. International Society for Optics and Photonics, 2015.
[12] Caron, Julien, et al. "Conical diffraction illumination opens the way for low phototoxicity super-resolution imaging." Cell adhesion & migration 8.5 (2014): 430-439.
[13] Fallet, Clément, et al. "Conical diffraction as a versatile building block to implement new imaging modalities for superresolution in fluorescence microscopy." Nanoimaging and Nanospectroscopy II. Vol. 9169. International Society for Optics and Photonics, 2014.
[14] Rosset, Sybille, Clement Fallet, and Gabriel Y. Sirat. "Focusing by a high numerical aperture lens of distributions generated by conical diffraction." Optics letters 39.23 (2014): 6569-6572.
用戶單位
法國巴斯德研究所 | 蒙彼利埃大學 |
相關產品
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3D單分子熒光成像系統-SAFe 360：http://www.dongsenyule.com/product/2019073110.shtml
