分享 收藏

大視野單分子超分辨模塊-SAFe180

品牌：法國abbelight
型號(hào)： abbelight
產(chǎn)地：歐洲法國
供應(yīng)商報(bào)價(jià)：面議

QUANTUM量子科學(xué)儀器貿(mào)易（北京）有限公司更新時(shí)間：2025-04-21 10:15:39

銷售范圍售全國

入駐年限第10年

營(yíng)業(yè)執(zhí)照已審核

同類產(chǎn)品成像系統(tǒng)(21件)

立即掃碼咨詢

聯(lián)系方式：4008558699轉(zhuǎn)8120

聯(lián)系我們時(shí)請(qǐng)說明在儀器網(wǎng)（www.vietnamtrade.org）上看到的!

掃碼分享

為您推薦

產(chǎn)品特點(diǎn)

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(dú)有的DASEY技術(shù)能夠極大的提高定位精度的同時(shí)，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(gè)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(jí)為超分辨顯微鏡。并且改造過程不會(huì)破壞原有顯微鏡系統(tǒng)的光路和功能，不會(huì)與其它的顯微鏡改造相沖突。

詳細(xì)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(gè)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(jí)為超分辨成像系統(tǒng)。并且改造過程不會(huì)破壞原有顯微鏡系統(tǒng)的光路和功能，不會(huì)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(gè)升級(jí)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(shí)，享受到經(jīng)濟(jì)合理的超分辨升級(jí)方案。

加裝

TIRF
PALM
STORM
SPT

smFRET

......

兼容

Confocal
Spinning-Desk
Widefield
SIM

STED

......

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(dòng)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(cè)試數(shù)據(jù)

大視野單分子超分辨模塊-SAFe180

超大的視野神經(jīng)元

大視野單分子超分辨模塊-SAFe180

偽足小體

大視野單分子超分辨模塊-SAFe180

模式生物

大視野單分子超分辨模塊-SAFe180

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.

用戶單位