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    3D單分子熒光成像系統(tǒng)-SAFe 360

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    產(chǎn)品特點

    這款產(chǎn)品使用突破性的DAISY技術(shù),能夠在保持高精度、大視野成像的同時,解決以往SMLM顯微鏡中不易解決的震動、熱、時間、不同波長染料等因素引起的漂移。

    詳細介紹

          SAFe 360是法國abbelight公司推出的一款基于單分子定位的顯微成像(SMLM)的新型3D單分子成像系統(tǒng),它獨有的DAISY技術(shù)整合了散光技術(shù)和超臨界角光技術(shù),能夠極大的提高定位精度,xyz三軸定位精度高達15nm,可以提供高清晰三維亞細胞結(jié)構(gòu)圖像,支持同時四色成像,可以用于細胞納米三維成像,觀測高清晰亞細胞器結(jié)構(gòu),實時研究不同的結(jié)構(gòu)功能蛋白的共定位信息,在單分子水平研究分子動力學(xué)反應(yīng)以及細胞間的相互作用等。


    加裝
    TIRF
    PALM
    STORM
    SPT

    smFRET

    ...... 


    兼容
    Confocal
    Spinning-Desk
    Widefield
    SIM

    STED

    ......


    設(shè)備參數(shù)


    + 成像模式:PALM、STORM、PAINT、smFRET 、SPT

    + 光源模式:Epi、TIRF、HILO

    分辨率:15 nm的XYZ軸分辨率

    超大視野:200 × 200 μm2的視野

    +  一次可同時采集1.2 μm深度圖像信息

    +  圖像深度:10 μm

    +  實時漂移矯正

    +  四色同時成像

    +  活細胞成像模式


    配套試劑


    Smart kit


    ?  10 doses per box

    ?  200 μL per dose

    ?  30 sec prepartion

    ?  2 months in a fridge

    ?  2 weeks on sample



    Compatible dyes


    ?  Atto 488, WGA-AF?488

    ?  AF?532, CF?532, Cy3b

    ?  AF?555, AF?594, CF?555, AF?568, CF?568, Cy5, MemBriteTM 568, TMR

    ?  AF?647, CF?647, AF?680, CF?680, MemBriteTM 640, Actin-stain 670, SiR647


    測試數(shù)據(jù)

    3D線粒體結(jié)構(gòu)

    核孔復(fù)合物

    老鼠海馬神經(jīng)元

    微管蛋白網(wǎng)絡(luò)


    發(fā)表文章

    [1] Radhakrishnan, A. V., et al. "Single-Protein Tracking to Study Protein Interactions During Integrin-Based Migration." The Integrin Interactome. Humana, New York, NY, (2021). 85-113.

    [2] Jouchet, Pierre, et al. "Nanometric axial localization of single fluorescent molecules with modulated excitation." Nature Photonics (2021): 1-8.

    [3] Pernier, Julien, et al. "Myosin 1b flattens and prunes branched actin filaments." Journal of cell science 133.18 (2020).

    [4] Jimenez, Angélique, Karoline Friedl, and Christophe Leterrier. "About samples, giving examples: optimized single molecule localization microscopy." Methods 174 (2020): 100-114.

    [5] Mau, Adrien, et al. "Fast scanned widefield scheme provides tunable and uniform illumination for optimized SMLM on large fields of view." bioRxiv (2020).

    [6] Orre, Thomas, et al. "Molecular motion and tridimensional nanoscale localization of kindlin control integrin activation in focal adhesions." bioRxiv (2020).

    [7] Cabriel, Clément, et al. "Combining 3D single molecule localization strategies for reproducible bioimaging." Nature communications 10.1 (2019): 1980.

    [8] Woodhams, Stephen G., et al. "Cell type–specific super-resolution imaging reveals an increase in calcium-permeable AMPA receptors at spinal peptidergic terminals as an anatomical correlate of inflammatory pain." Pain 160.11 (2019): 2641-2650.

    [9] Belkahla, Hanen, et al. "Carbon dots, a powerful non-toxic support for bioimaging by fluorescence nanoscopy and eradication of bacteria by photothermia." Nanoscale Advances (2019).

    [10] Denis, Kevin, et al. "Targeting Type IV pili as an antivirulence strategy against invasive meningococcal disease." Nature microbiology 4.6 (2019): 972.

    [11] Szabo, Quentin, et al. "TADs are 3D structural units of higher-order chromosome organization in Drosophila." Science advances 4.2 (2018): eaar8082. 

    [12] Boudjemaa, Rym, et al. "Impact of bacterial membrane fatty acid composition on the failure of daptomycin to kill Staphylococcus aureus." Antimicrobial agents and chemotherapy 62.7 (2018): e00023-18.

    [13] Culley, Sian, et al. "Quantitative mapping and minimization of super-resolution optical imaging artifacts." Nature methods 15.4 (2018): 263.

    [14] Berger, Stephen L., et al. "Localized myosin II activity regulates assembly and plasticity of the axon initial segment." Neuron 97.3 (2018): 555-570.

    [15] Cabriel, Clément, et al. "Aberration-accounting calibration for 3D single-molecule localization microscopy." Optics letters 43.2 (2018): 174-177. 

    [16] Bouissou, Ana?s, et al. "Podosome force generation machinery: a local balance between protrusion at the core and traction at the ring." ACS nano 11.4 (2017): 4028-4040. 

    [17] Sellés, Julien, et al. "Nuclear pore complex plasticity during developmental process as revealed by super-resolution microscopy." Scientific reports 7.1 (2017): 14732.

    [18] Bourg, Nicolas, et al. "Direct optical nanoscopy with axially localized detection." Nature Photonics 9.9 (2015): 587.


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