define fluorescence - EAS

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  1. Fluorescence - Wikipedia

    https://en.wikipedia.org/wiki/Fluorescence

    Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation.It is a form of luminescence.In most cases, the emitted light has a longer wavelength, and therefore a lower photon energy, than the absorbed radiation. A perceptible example of fluorescence occurs when the absorbed radiation is in the ultraviolet …

  2. Fluorescence Polarization (FP) | Molecular Devices

    https://www.moleculardevices.com/technology/fluorescence-polarization

    Fluorescence polarization (FP) is a technique that is widely used to monitor binding events in solution. It can be used to assess biomolecular interactions, including protein-antibody binding and DNA hybridization, as well as enzyme activity, and it has been adapted to basic research as well as high-throughput screening.

  3. Fluorescence lifetime imaging microscopy: fundamentals and ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219965

    May 13, 2020 · Fluorescence is a radiative process in which molecules (fluorophores) decay to the ground state by emitting detectable photons (on the timescale of 10 − 9 s).The fluorescence emission happens from the lowest excited electronic level (S 1).This mandatory emission from the lowest excited electronic level ensures that the emission spectrum remains the same and …

  4. Fluorescence - Chemistry LibreTexts

    https://chem.libretexts.org/.../Fluorescence

    Aug 15, 2020 · Another way to define the fluorescence quantum yield is by the excited state decay rates: \[ \Phi = \dfrac{k_f}{\sum_i k_i} \label{Eq1}\] where \(k_f\) is the rate of spontaneous emission of radiation and the denominator is the sum of all rates of excited state decay for each deactivation process (ie phosphorescence, intersystem crossing ...

  5. FACS - Fluorescence Activated Cell Sorting • iBiology

    https://www.ibiology.org/techniques/facs

    00:00:28.15 FACS is the abbreviation for fluorescence activated cell sorting, 00:00:31.20 and many people say FACS 00:00:34.21 when they just mean flow cytometry, 00:00:37.20 as as shown here in the cartoon on the right side. 00:00:41.23 So, here we have a single cell suspension 00:00:45.16 labeled with fluorescent dyes, which we bring, here,

  6. A technical review and guide to RNA fluorescence in situ ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085896

    Mar 19, 2020 · RNA-fluorescence in situ hybridization (FISH) is a powerful tool to visualize target messenger RNA transcripts in cultured cells, tissue sections or whole-mount preparations. As the technique has been developed over time, an ever-increasing number of divergent protocols have been published.

  7. Sample Preparation for Fluorescence Microscopy: An ...

    https://www.biotek.com/resources/white-papers/...

    Fluorescence microscopy of live cells uses either genetically encoded fluorescent proteins (e.g. GFP, mcherry, YFP, RFP, etc.) or cell membrane-permeable, non-toxic fluorescent stains. Fluorescence microscopy of fixed cells uses a fixative agent that renders the cells dead, but maintains cellular structure, allowing the use of specific ...

  8. Detection by thresholding · Analyzing fluorescence ...

    https://petebankhead.gitbooks.io/imagej-intro/...

    The usual way to generate a binary image is by thresholding: identifying pixels above or below a particular threshold value.In ImageJ, the Image Adjust Threshold… command allows you to define both low and high threshold values, so that only pixels falling within a specified range are found. After choosing suitable thresholds, pressing Apply produces the binary image [].

  9. Polarization modulation with optical lock-in detection ...

    https://www.nature.com/articles/s41377-021-00689-1

    Jan 01, 2022 · OLID via polarization modulation. In FPM, the background noise can easily overwhelm the weak polarized fluorescence signal. Background noise could come from various sources, such as the scattered ...

  10. www.flowlab-childrens-harvard.com/yahoo_site_admin/...

    Drag to draw a gate to set the range of fluorescence values that will define FL1 positive cells. Name this subset FL1+. Click the plus sign to add the name to the list for future use. Click OK. There are several gating tools for bivariate plots. Rectangle, Polygon, Quadrant or Ellipse gating tools can be selected from the top of the Graph



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