大视野单分子超分辨模块-SAFe 180

 

    abbelight SAFe180是一款基于单分子定位技术的显微成像（SMLM）的超分辨模块。该设备具有高度灵活性，能够搭载在大多数的倒置显微镜上，并且仅仅需要使用一个C-mount（CCD或CMOS所连接的部位）接口，即可将您的倒置显微镜直接升为超分辨成像系统。并且改造过程不会破坏原有显微镜系统的光路和功能，不会与其它的显微镜改造相冲突。

    本设备既在配置上的选择也十分灵活。它既可以作为显微镜的一个升配件来改造您的显微镜，也拥有完整的超分辨系统。让用户在获得专业的图像质量的同时，获得经济合理的超分辨升方案。

大视野单分子超分辨模块-SAFe 180

 

设备参数

+  模块化系统：可接到大多数倒置荧光显微镜

+  成像模式：PALM、STORM、smFRET、PAINT、SPT

+  光源模式：Epi、TIRF、HILO

+  超高分辨率：25 nm的XY轴分辨率，50nm的Z轴分辨率

+  超大视野：180 × 180 μm²的视野

+  全自动化控制

+  无需高功率激光光源

 

加装 TIRF PALM STORM SPT smFRET ......

兼容 Confocal Spinning-Desk Widefield SIM STED

 

Now We See......

超大的视野神经元	伪足小体
模式生物	微管蛋白

 

配套试剂

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

 

发表文献列表 

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

[2] 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.

[3] 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).

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

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

[6] 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.

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

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

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

[10] Bouissou, Anaïs, 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. 

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

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

用户单位
 

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