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    模塊化超分辨共聚焦顯微系統(tǒng)-LiveCodim

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    產(chǎn)品特點(diǎn)

    產(chǎn)品優(yōu)勢(shì)



    · 超高性價(jià)比:模塊化超分辨,節(jié)省成本,兼容絕大多數(shù)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(xì)胞成像:低光毒性和光漂白性,適合活細(xì)胞成像

    · 制樣簡(jiǎn)單:樣品無需特殊處理,無需特殊染料

    · 全自動(dòng)軟件:全自動(dòng)調(diào)節(jié)各種參數(shù),簡(jiǎn)單易上手

    詳細(xì)介紹


    模塊化超分辨共聚焦顯微系統(tǒng)-LiveCodim


        傳統(tǒng)熒光顯微鏡受到光學(xué)衍射極限的影響,高的分辨率為200 nm,因此很難觀察細(xì)胞中的超微結(jié)構(gòu)。LiveCodim是一款模塊化超分辨共聚焦顯微系統(tǒng),能夠適配絕大多數(shù)的倒置熒光顯微鏡,將現(xiàn)有的倒置顯微鏡升級(jí)成為具備寬場(chǎng)、共聚焦、超分辨三大模式的成像系統(tǒng)。LiveCodim通過獨(dú)特的錐形衍射顯微鏡—— 一種強(qiáng)大的波束成形器,能夠直接提供分辨率高達(dá)120 nm的實(shí)時(shí)活細(xì)胞超分辨共聚焦成像,同時(shí)無需對(duì)樣品進(jìn)行任何額外操作,結(jié)合其低光毒性,以及方便快捷的操作系統(tǒng)等優(yōu)勢(shì),非常適合拍攝熒光成像。


    產(chǎn)品優(yōu)勢(shì)

    ·  超高性價(jià)比:模塊化超分辨,節(jié)省成本,兼容絕大多數(shù)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(xì)胞成像:低光毒性和光漂白性,適合活細(xì)胞成像

    ·  制樣簡(jiǎn)單:樣品無需特殊處理,無需特殊染料

    ·  全自動(dòng)軟件:全自動(dòng)調(diào)節(jié)各種參數(shù),簡(jiǎn)單易上手


    主要參數(shù)

    ·  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(chǎng)、共聚焦、LiveCodim超分辨

    ·  四色成像通道:405 nm, 488 nm, 561 nm, 640 nm (根據(jù)需求可增加)


    測(cè)試數(shù)據(jù)

    1. MDCK細(xì)胞中線粒體的動(dòng)態(tài)變化

    MDCK細(xì)胞中線粒體的動(dòng)態(tài)變化_gaitubao_1000x412.gif


    2.  Hela胞的微管寬場(chǎng),共聚焦,LiveCodim超分辨成像

    2021_11_9_10273342.png


    3.  細(xì)胞分裂中期的COS-7細(xì)胞3D多色超分辨成像

    細(xì)胞3D多色成像-壓縮版.gif



    4.  植物細(xì)胞成像:觀測(cè)鈴蘭草的根莖


    2021_11_9_515823342.png


    5.  天然免疫分子TRIM5α作用機(jī)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(fā)病速度的重要因素,其抗病毒活性通常通過小泛素相關(guān)修飾物(SUMO)調(diào)節(jié),但是具體的作用機(jī)制仍有待進(jìn)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(shí)與存在于核孔的細(xì)胞質(zhì)絲上的RanGTPase激活蛋白R(shí)anGAP1有明顯的共定位現(xiàn)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(xì)胞的胞質(zhì)面。

    2021_11_9_423383689.png



    部分發(fā)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  

    2021_11_9_1343552772.jpg

    法國(guó)巴斯德研究所


    2021_11_9_287988137.jpg

    蒙彼利埃大學(xué)  



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