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大视野单分子超分辨模块-SAFe180

QUANTUM量子科学仪器贸易(北京)有限公司

企业性质生产商

入驻年限第6年

营业执照已审核
同类产品成像系统(22件)

    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,能够搭载在绝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级为超分辨成像系统。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级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,享受到经济合理的超分辨升级方案。


加装
TIRF
PALM
STORM
SPT

smFRET

...... 


兼容
Confocal
Spinning-Desk
Widefield
SIM

STED

......


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


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


测试数据

大视野单分子超分辨模块-SAFe180

超大的视野神经元

大视野单分子超分辨模块-SAFe180

伪足小体

大视野单分子超分辨模块-SAFe180

模式生物

大视野单分子超分辨模块-SAFe180

微管蛋白


发表文章

[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. 


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