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by
Tan, Metin, author.
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fluorescence quenching where intensity average lifetime decreases below 1 ns. Separating these layers with an
by
Sayar, Melike, author.
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and high cost or requiring of sophisticated procedures. However, fluorescence analysis has high
by
Batı, Gizem, author.
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are not known. Using fluorescence microscopy and antibodies that recognize actin, cortactin and MT1
by
Kanlı, Ali İhsan, author.
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fluorescence spectrum measurements in the UV-VIS range (vascular volume, oxygenation, extra cellular matrix
by
Yersel, Müşerref.
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reflectance (FTIR-ATR) accessory, and fluorescence spectrophotometer (synchronous fluorescence mode and 3D
by
Önol, Ayşenur Başar, author.
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20%, respectively. Fluorescence spectrophotometry determined Doxorubicin loading, showing
by
Karabıyık, Merve, author.
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film based quantum dot-nitroxide radical fluorescence sensor nanoprobe, which has a multi-use property
by
Meşe Sezen, Ayten Ekin, author.
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spectroscopic methods which are UV-Vis, Fluorescence, FT-NIR and FTIR-ATR spectroscopy, were performed and
by
Chilufya, Langson, author.
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of the organic moiety use was a BODIPY-type organic dye, the fluorescence properties of these newly
by
Başlar, Muhammet Semih, author.
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), and screened for improved peroxidation activity. Additionally, fluorescence based Amplex Red
by
Yırtıcı, İlayda Melek, author.
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fluorescence peak was not observed. Therefore, the further study was continued with MPA capped ZnS xSe1-x
by
Arslan, Nurhan, author.
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fluorochrome-conjugated target proteins in a cell through fluorescence following excitation. We thirdly simulated the
43 sonuç bulundu
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