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          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360
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          • 3D單分子熒光成像系統-SAFe 360
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          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

            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,它的DAISY技術整合了散光技術和超臨界角光技術,能夠大的提高定位精度,xyz三軸定位精度高達15nm,可以提供高清晰三維亞細胞結構圖像,支持同時多四色成像,可以用于細胞納米三維成像,觀測高清晰亞細胞器結構,實時研究不同的結構功能蛋白的共定位信息,在單分子水平研究分子動力學反應以及細胞間的相互作用等。

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

            

          設備參數

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

            +  光源模式:Epi、TIRF、HILO

            +  超高分辨率: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

          加裝TIRF

          PALM

          STORM

          SPT

          smFRET

          ...... 

          兼容Confocal

          Spinning-Desk

          Widefield

          SIM

          STED

          3D單分子熒光成像系統-SAFe 360

            

          Now We See......

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D線粒體結構核孔復合物

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          老鼠海馬神經元微管蛋白網絡

            

          配套試劑

          SmartkitCompatibledyes

          - 10 doses per box

          - 200 μL per dose

          - 30 sec prepartion

          - 2 months in a fridge

          - 2 weeks on sample

          - 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

            

          發表文獻列表

            [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 science133.18 (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 communications10.1 (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." Pain160.11 (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 microbiology4.6 (2019): 972.

            [11] Szabo, Quentin, et al. "TADs are 3D structural units of higher-order chromosome organization in Drosophila." Science advances4.2 (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 chemotherapy62.7 (2018): e00023-18.

            [13] Culley, Sian, et al. "Quantitative mapping and minimization of super-resolution optical imaging artifacts." Nature methods15.4 (2018): 263.

            [14] Berger, Stephen L., et al. "Localized myosin II activity regulates assembly and plasticity of the axon initial segment." Neuron97.3 (2018): 555-570.

            [15] Cabriel, Clément, et al. "Aberration-accounting calibration for 3D single-molecule localization microscopy." Optics letters43.2 (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 nano11.4 (2017): 4028-4040. 

            [17] Sellés, Julien, et al. "Nuclear pore complex plasticity during developmental process as revealed by super-resolution microscopy." Scientific reports7.1 (2017): 14732.

            [18] Bourg, Nicolas, et al. "Direct optical nanoscopy with axially localized detection." Nature Photonics9.9 (2015): 587. 

            

          用戶單位

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360

          3D單分子熒光成像系統-SAFe 360


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