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            當(dāng)前位置:QUANTUM量子科學(xué)儀器貿(mào)易(北京)有限公司>>生命科學(xué)>>3D單分子熒光成像系統(tǒng)-SAFe 360

            3D單分子熒光成像系統(tǒng)-SAFe 360

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            所  在  地:北京市

            更新時(shí)間:2024-04-18 11:31:38瀏覽次數(shù):2694

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            產(chǎn)地類別 進(jìn)口 價(jià)格區(qū)間 面議
            儀器種類 光學(xué)成像 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,生物產(chǎn)業(yè),制藥/生物制藥,綜合
            abbelight 3D單分子熒光成像系統(tǒng)-SAFe 360是款基于單分子定位的顯微成像(SMLM)的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可同時(shí)高達(dá)15nm的定位精度

            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
            PALM
            STORM
            SPT

            smFRET

            ......


            兼容

            Confocal
            Spinning-Desk
            Widefield
            SIM

            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

            [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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