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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 | 2022-03-21T11:30:30Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:30:30Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Kumari, P., Verma, S. K., & Mobin, S. M. (2019). A facile two-photon fluorescent probe: An endoplasmic reticulum tracker monitoring ER stress and vesicular transport to lysosomes. Chemical Communications, 55(3), 294-297. doi:10.1039/C8CC07429A | en_US |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.other | EID(2-s2.0-85059405482) | - |
dc.identifier.uri | https://doi.org/10.1039/C8CC07429A | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/8975 | - |
dc.description.abstract | The morphological divergence of the Endoplasmic Reticulum (ER) during stress is a powerful indicator of several diseases. A new two-photon, non-cytotoxic, fluorescent probe (ERLp) was designed and synthesized in a facile manner for selective tracking of the Endoplasmic Reticulum (ER) with a high Pearson co-localization coefficient (0.91) in live cells and tumor spheroids. Further, ER stress during cell apoptosis and vesicular transport from the ER to the lysosomal compartment were also explored by employing ERLp. Therefore, ERLp can be used as a potent tool for examining vesicle transport or ER stress associated diseases in real time. © 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 | acetonitrile | en_US |
dc.subject | fluorescent dye | en_US |
dc.subject | phosphate buffered saline | en_US |
dc.subject | fluorescent dye | en_US |
dc.subject | A-375 cell line | en_US |
dc.subject | absorption spectroscopy | en_US |
dc.subject | apoptosis | en_US |
dc.subject | Article | en_US |
dc.subject | biocompatibility | en_US |
dc.subject | cell tracking | en_US |
dc.subject | cell transport | en_US |
dc.subject | cellular distribution | en_US |
dc.subject | confocal microscopy | en_US |
dc.subject | controlled study | en_US |
dc.subject | crystal structure | en_US |
dc.subject | DU145 cell line | en_US |
dc.subject | endoplasmic reticulum | en_US |
dc.subject | endoplasmic reticulum stress | en_US |
dc.subject | flow cytometry | en_US |
dc.subject | fluorescence | en_US |
dc.subject | fluorescence microscopy | en_US |
dc.subject | Fourier transform infrared spectroscopy | en_US |
dc.subject | HeLa cell line | en_US |
dc.subject | hydrophobicity | en_US |
dc.subject | live cell imaging | en_US |
dc.subject | lysosome | en_US |
dc.subject | mass spectrometry | en_US |
dc.subject | MCF-7 cell line | en_US |
dc.subject | multiphoton microscopy | en_US |
dc.subject | polymerization | en_US |
dc.subject | proton nuclear magnetic resonance | en_US |
dc.subject | single cell analysis | en_US |
dc.subject | synthesis | en_US |
dc.subject | tumor spheroid | en_US |
dc.subject | vesicular transport | en_US |
dc.subject | X ray diffraction | en_US |
dc.subject | chemistry | en_US |
dc.subject | human | en_US |
dc.subject | lysosome | en_US |
dc.subject | metabolism | en_US |
dc.subject | multicellular spheroid | en_US |
dc.subject | neoplasm | en_US |
dc.subject | pathology | en_US |
dc.subject | photon | en_US |
dc.subject | transport vesicle | en_US |
dc.subject | Apoptosis | en_US |
dc.subject | Endoplasmic Reticulum | en_US |
dc.subject | Endoplasmic Reticulum Stress | en_US |
dc.subject | Fluorescent Dyes | en_US |
dc.subject | Humans | en_US |
dc.subject | Lysosomes | en_US |
dc.subject | Neoplasms | en_US |
dc.subject | Photons | en_US |
dc.subject | Spheroids, Cellular | en_US |
dc.subject | Transport Vesicles | en_US |
dc.title | A facile two-photon fluorescent probe: an endoplasmic reticulum tracker monitoring ER stress and vesicular transport to lysosomes | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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