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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全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

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            所  在  地:北京市

            更新時(shí)間:2025-04-11 07:29:34瀏覽次數(shù):2217

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            產(chǎn)地類別 進(jìn)口 應(yīng)用領(lǐng)域 生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥
            顆粒大小分辨范圍 大于50 nm(可分析大于40 nm的病毒顆粒) 熒光粒徑分辨范圍 大于20 nm
            所需樣本體積 25 μL 激發(fā)波長 410 nm,488 nm,555 nm,640 nm
            可一次檢測 16個(gè)樣本,每個(gè)樣本可同時(shí)檢測6個(gè)不同亞型及3種生物標(biāo)記的熒 單個(gè)樣品檢測時(shí)間 8分鐘
            捕獲抗體 一個(gè)芯片最多允許6種捕獲抗體(+陰性對照) 熒光通道 3個(gè)熒光通道
            法國Abbelight公司開發(fā)的3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)是一款無需純化的、全自動(dòng)的可對單個(gè)外泌體進(jìn)行表征分析的全新設(shè)備。該設(shè)備能夠提供外泌體表征信息,包括外泌體粒徑大小、亞型分布、攜帶蛋白表達(dá)、單個(gè)外泌體的膜蛋白與生物標(biāo)志物共定位等。操作簡單,結(jié)果可靠。

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            法國Abbelight公司開發(fā)的3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)是一款無需純化的、全自動(dòng)的可對單個(gè)外泌體進(jìn)行表征分析的全新設(shè)備。該設(shè)備能夠提供外泌體表征信息,包括外泌體粒徑大小、亞型分布、攜帶蛋白表達(dá)、單個(gè)外泌體的膜蛋白與生物標(biāo)志物共定位等。操作簡單,結(jié)果可靠。

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)基于特異性免疫捕獲技術(shù),允許研究者直接分析特定群體的外泌體。通過單分子定位技術(shù)成像,可以得到單個(gè)外泌體的超分辨成像結(jié)果,尺度可以到20nm。全自動(dòng)外泌體熒光檢測分析系統(tǒng)兼容各種生物樣本,除了純化的外泌體之外,對于血液、尿液、惡性腫瘤、腹水中的外泌體也可直接檢測分析,大大拓展了研究范圍。

            應(yīng)用方向及主要特征

             

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            超高分辨單外泌體成像

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            左:2D單個(gè)外泌體成像;右:3D單個(gè)外泌體成像

            外泌體粒徑分析:通過團(tuán)簇分析外泌體的整體和亞群的粒徑分布

            膜蛋白表征與共定位分析,以CD63,CD81&CD9為例表征其單陽,雙陽和三陽的比例

             

             

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            外泌體內(nèi)容物表征

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            對比穿膜處理后外泌體中內(nèi)容物aGFP的表達(dá)

            觀測細(xì)胞中外泌體的分布情況,研究細(xì)胞中細(xì)胞器或者其他蛋白和外泌體的定位關(guān)系

             

            應(yīng)用案例

             

            法國Abbelight公司開發(fā)的3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)是一款無需純化的、全自動(dòng)的可對單個(gè)外泌體進(jìn)行表征分析的全新設(shè)備。該設(shè)備能夠提供單個(gè)外泌體表征信息,包括外泌體粒徑大小、亞型分布、攜帶蛋白表達(dá)、單個(gè)外泌體的膜蛋白與生物標(biāo)志物共定位等。

            應(yīng)用領(lǐng)域:腫瘤診斷,藥系統(tǒng)開發(fā),眼科疾病診斷,疫苗研發(fā),脊髓受傷機(jī)制研究,血漿/血清外泌體分析,外泌體工程化,呼吸疾病診斷

            測試數(shù)據(jù)

            外泌體2D成像

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

            外泌體3D成像

             

            外泌體形態(tài)分析

            3D全自動(dòng)外泌體熒光檢測分析系統(tǒng)

             

            發(fā)表文章

            [1] Storci, Gianluca, et al. "CAR+ extracellular vesicles predict ICANS in patients with B cell lymphomas treated with CD19-directed CAR T cells." The Journal of Clinical Investigation 134.14 (2024).

            [2] Huang, Xiaowan, et al. "Nanoreceptors promote mutant p53 protein degradation by mimicking selective autophagy receptors." Nature Nanotechnology (2024): 1-9.

            [3] Ye, Qian-Ni, et al. "Orchestrating NK and T cells via tri-specific nano-antibodies for synergistic antitumor immunity." Nature Communications 15.1 (2024): 6211.

            [4] Shafaq-Zadah, Massiullah, et al. "Exploration into Galectin-3 Driven Endocytosis and Lattices." Biomolecules 14.9 (2024): 1169.

            [5] Sanchez-Londono, Mariana, et al. "Visualization of Type IV-A1 CRISPR-mediated repression of gene expression and plasmid replication." Nucleic Acids Research 52.20 (2024): 12592-12603.

            [6] Rajbanshi B, Guruacharya A, Mandell J W, et al. Localization, induction, and cellular effects of tau phosphorylated at threonine 217 1[J]. Alzheimer's & Dementia, 2023, 19(7): 2874-2887.

            [7] Friedl, Karoline, et al. "Robust and fast multicolor Single Molecule Localization Microscopy using spectral separation and demixing." BioRxiv (2023): 2023-01.

            [8] Baschieri, Francesco, et al. "Fibroblasts generate topographical cues that steer cancer cell migration." Science Advances 9.33 (2023): eade2120.

            [9] Wessel, Aimee K., et al. "Escherichia coli SPFH membrane microdomain proteins HflKC contribute to aminoglycoside and oxidative stress tolerance." Microbiology Spectrum 11.4 (2023): e01767-23.

            [10] Liu, Wei, et al. "Mitofusin-2 regulates leukocyte adhesion and β2 integrin activation." Journal of leukocyte biology 111.4 (2022): 771-791.

            [11] Rajbanshi, Binita, et al. "Localization, induction, and cellular effects of tau phosphorylated at threonine 217." Alzheimer's & Dementia (2023).

            [12] Pagliuca, M., et al. "38P Single molecule localization microscopy for extracellular vesicles detection in cancer." Annals of Oncology 33 (2022): S1395-S1396.

            [13] Robaszkiewicz, A., and K. Gronkowska. "36P EP300 as an epigenetic target in p53 wild-type tumors treated with cisplatin." Annals of Oncology 33 (2022): S1395.

            [14] He, Jin, et al. "Heterozygous Seryl‐tRNA Synthetase 1 Variants Cause Charcot–Marie–Tooth Disease." Annals of Neurology (2022).

            [15] Gazzola, Morgan, et al. "Microtubules self-repair in living cells." Current Biology (2022).

            [16] Liu, Wei, et al. "Mitofusin‐2 regulates leukocyte adhesion and β2 integrin activation." Journal of Leukocyte Biology 111.4 (2022): 771-791.

            [17] Portes, Marion, et al. "Nanoscale architecture and coordination of actin cores within the sealing zone of human osteoclasts." Elife 11 (2022): e75610.

            [18] Wessel, Aimee K., et al. "Escherichia coli membrane microdomain SPFH protein HflC interacts with YajC and contributes to aminoglycoside and oxidative stress tolerance." bioRxiv (2022).

            [19] 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.

            [20] Jouchet, Pierre, et al. "Nanometric axial localization of single fluorescent molecules with modulated excitation." Nature Photonics (2021): 1-8.

            [21] Orré, Thomas, et al. "Molecular motion and tridimensional nanoscale localization of kindlin control integrin activation in focal adhesions." Nature Communications 12.1 (2021): 3104.

            [22] Pernier, Julien, et al. "Myosin 1b flattens and prunes branched actin filaments." Journal of cell science 133.18 (2020).

            [23] Jimenez, Angélique, Karoline Friedl, and Christophe Leterrier. "About samples, giving examples: optimized single molecule localization microscopy." Methods 174 (2020): 100-114.

            [24] Mau, Adrien, et al. "Fast scanned widefield scheme provides tunable and uniform illumination for optimized SMLM on large fields of view." bioRxiv (2020).

            [25] Cabriel, Clément, et al. "Combining 3D single molecule localization strategies for reproducible bioimaging." Nature Communications 10.1 (2019): 1980.

            [26] 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.

            [27] 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).

            [28] Denis, Kevin, et al. "Targeting Type IV pili as an antivirulence strategy against invasive meningococcal disease." Nature microbiology 4.6 (2019): 972.

            [29] Szabo, Quentin, et al. "TADs are 3D structural units of higher-order chromosome organization in Drosophila." Science advances 4.2 (2018): eaar8082.

            [30] 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.

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