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大視野單分子超分辨模塊-SAFe180
- 品牌:法國abbelight
- 型號: abbelight
- 產(chǎn)地:歐洲 法國
- 供應(yīng)商報價:面議
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QUANTUM量子科學(xué)儀器貿(mào)易(北京)有限公司
更新時間:2025-04-21 10:15:39
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銷售范圍售全國
入駐年限第10年
營業(yè)執(zhí)照已審核
- 同類產(chǎn)品成像系統(tǒng)(21件)
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產(chǎn)品特點
- abbelight是一款模塊化的多功能的單分子定位顯微鏡(SMLM)系統(tǒng),它獨有的DASEY技術(shù)能夠極大的提高定位精度的同時,還保持在較小的尺寸。該設(shè)備具有高度靈活性,能夠搭載在絕大多數(shù)的倒置顯微鏡上,并且僅僅需要使用一個C-mount(CCD或CMOS所連接的部位)接口,即可將您的倒置顯微鏡直接升級為超分辨顯微鏡。并且改造過程不會破壞原有顯微鏡系統(tǒng)的光路和功能,不會與其它的顯微鏡改造相沖突。
詳細介紹
abbelight SAFe180是一款基于單分子定位技術(shù)的顯微成像(SMLM)的超分辨模塊。該設(shè)備具有高度靈活性,能夠搭載在絕大多數(shù)的倒置顯微鏡上,并且僅僅需要使用一個C-mount(CCD或CMOS所連接的部位)接口,即可將您的倒置顯微鏡直接升級為超分辨成像系統(tǒng)。并且改造過程不會破壞原有顯微鏡系統(tǒng)的光路和功能,不會與其它的顯微鏡改造相沖突。
本設(shè)備既在配置上的選擇也十分靈活。它既可以作為顯微鏡的一個升級配件來改造您的顯微鏡,也擁有完整的超分辨系統(tǒng)。讓用戶在獲得專業(yè)的圖像質(zhì)量的同時,享受到經(jīng)濟合理的超分辨升級方案。
加裝 TIRF
PALM
STORM
SPTsmFRET
......
兼容 Confocal
Spinning-Desk
Widefield
SIMSTED
......
設(shè)備參數(shù)
+ 模塊化系統(tǒng):可接到大多數(shù)倒置熒光顯微鏡
+ 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軸分辨率,50nm的Z軸分辨率
+ 超大視野:180 × 180 μm2的視野
+ 全自動化控制
+ 無需高功率激光光源
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
測試數(shù)據(jù)
超大的視野神經(jīng)元
偽足小體
模式生物
微管蛋白
發(fā)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, Sian, 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, 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.
[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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