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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Mobin, Shaikh M. | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:30:58Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:30:58Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Kumari, P., Verma, S. K., & Mobin, S. M. (2018). Water soluble two-photon fluorescent organic probes for long-term imaging of lysosomes in live cells and tumor spheroids. Chemical Communications, 54(5), 539-542. doi:10.1039/c7cc07812a | en_US |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.other | EID(2-s2.0-85040542394) | - |
dc.identifier.uri | https://doi.org/10.1039/c7cc07812a | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9080 | - |
dc.description.abstract | The morphological alteration of lysosomes is a powerful indicator of various pathological disorders. In this regard, we have designed and synthesized a new water soluble fluorescent Schiff-base ligand (L-lyso) containing two hydroxyl groups. L-lyso exhibits excellent two-photon properties with tracking of lysosomes in live cells as well as in 3D tumor spheroids. Furthermore, it can label lysosomes for more than 3 days. Thus, L-lyso has an edge over the commercially available expensive LysoTracker probes and also over other reported probes in terms of its long-term imaging, water solubility and facile synthesis. © 2018 The Royal Society of Chemistry. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.source | Chemical Communications | en_US |
dc.subject | Article | en_US |
dc.subject | bleaching | en_US |
dc.subject | controlled study | en_US |
dc.subject | crystallization | en_US |
dc.subject | endocytosis | en_US |
dc.subject | flow cytometry | en_US |
dc.subject | human | en_US |
dc.subject | human cell | en_US |
dc.subject | hydrophilicity | en_US |
dc.subject | image analysis | en_US |
dc.subject | live cell imaging | en_US |
dc.subject | lysosome | en_US |
dc.subject | molecular probe | en_US |
dc.subject | morphology | en_US |
dc.subject | multiphoton microscopy | en_US |
dc.subject | nuclear magnetic resonance spectroscopy | en_US |
dc.subject | oxidative phosphorylation | en_US |
dc.subject | protein localization | en_US |
dc.subject | synthesis | en_US |
dc.subject | tumor spheroid | en_US |
dc.subject | water soluble two photon fluorescent organic probe | en_US |
dc.subject | cell survival | en_US |
dc.subject | chemical structure | en_US |
dc.subject | chemistry | en_US |
dc.subject | fluorescence | en_US |
dc.subject | fluorescence imaging | en_US |
dc.subject | HeLa cell line | en_US |
dc.subject | lysosome | en_US |
dc.subject | multicellular spheroid | en_US |
dc.subject | pathology | en_US |
dc.subject | photon | en_US |
dc.subject | solubility | en_US |
dc.subject | fluorescent dye | en_US |
dc.subject | water | en_US |
dc.subject | Cell Survival | en_US |
dc.subject | Fluorescence | en_US |
dc.subject | Fluorescent Dyes | en_US |
dc.subject | HeLa Cells | en_US |
dc.subject | Humans | en_US |
dc.subject | Lysosomes | en_US |
dc.subject | Molecular Structure | en_US |
dc.subject | Optical Imaging | en_US |
dc.subject | Photons | en_US |
dc.subject | Solubility | en_US |
dc.subject | Spheroids, Cellular | en_US |
dc.subject | Water | en_US |
dc.title | Water soluble two-photon fluorescent organic probes for long-term imaging of lysosomes in live cells and tumor spheroids | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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