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3D單分子熒光成像系統(tǒng)-SAFe 360簡(jiǎn)介：
SAFe 360是法國(guó)abbelight公司推出的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*的DAISY技術(shù)整合了散光技術(shù)和超臨界角光技術(shù)，能夠很大的提高定位精度，xyz三軸定位精度高達(dá)15nm，可以提供高清晰三維亞細(xì)胞結(jié)構(gòu)圖像，支持同時(shí)多四色成像，可以用于細(xì)胞納米三維成像，觀測(cè)高清晰亞細(xì)胞器結(jié)構(gòu)，實(shí)時(shí)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(dòng)力學(xué)反應(yīng)以及細(xì)胞間的相互作用等。
| 加裝 | TIRF smFRET ...... | 兼容 | Confocal STED ...... |
3D單分子熒光成像系統(tǒng)-SAFe 360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
+ 次可同時(shí)采集1.2 μm深度圖像信息
+ 圖像深度：10 μm
+ 實(shí)時(shí)漂移矯正
+ 四色同時(shí)成像
+ 活細(xì)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(cè)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
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[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).
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[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.
用戶單位
