小样品，固体样品中荧光检测方案(分子荧光光谱)

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Fluorescence on Small or Solid Samples Sensitivity to small samples Samples can be valuable. Eitheryou don’t want to waste them， or youmay not have very much starting mate-rial. Biological proteins and enzymes， forexample， are often obtained in small vol-umes and may be expensive. In a mate-rials-science application， you may haveaccess only to a single fine crystal or aminute slice of a polymer. Fig. 1. Emission spectra of 20 nM resorufin us-ing the flowcell and cuvette. Signal-level is main-tained no matter what volume of sample is used.lnset is a comparative sketch of the 4 mL cu-vette and 20 pL flowcell. That'swhen the fine imagingquality and photon-counting sensitivityof the FluoroMax and Fluorolog@ spec-trofluorometers are essential. In Figure1， the signal level is maintained with ei-ther the 4-mL (#1920 or 1925) or the20-pL(#1955) cell containing indenticalsamples. A variety of reduced-volumecells (20 pL， 50 pL， 250 pL， and 1 mL)are available for all your fluorescenceneeds. Front-face fluorescence detection For highly concentrated， opaque，or solid samples such as blood， paint，optical brighteners， living cells， polymerfilms， or phosphors， front-face fluores-cence detection offers many advantagesfor quantitative and qualitative fluores-cence measurements.Concentratedand opaque liquids typically suffer fromself-absorption and complete attenua-tion of the beam. When measuring fluo-rescence at 90°， intensity measure-ments may be unreproducible or unde-tectable， and the excitation or emissionspectra may appear distorted. Front-face detection solves these problems(see Fig.2). Fig. 2. Comparison of fluorescence emissionfrom sickle-cell hemoglobin using right-angledetection and front-face detection. The B-37tryptophan is primarily responsible for this fluo-rescence. Front-face detection for opaqueliquids and solids can be an importantanalytical tool for characterizing fluores-cence of various sample types (See Fig.3). In the front-face technique， the exci-tation light is focused to the front surfaceof the samples and then fluorescenceemission is collected from the same re- gion at an angle that minimizes reflectedand scattered light. Fig. 3. Comparison of fluorescence emissionsignals from three contact-lens samples. Thesespectra can be used to determine if protein fromtears adhered to the lens surface. Contact-lensmanufacturers must verify that enzymatic clean-ers actually remove these proteins. (A) Tyrosine；(B) tryptophan； (C) enzymatically cleaned lens.This verifies that the solution actually cleanedthe lens. For our Fluorolog@ modular spec-trofluorometer， use the 22.5°collection- path for liquid and solid samples. Forourbench-top FluoroMaxspectro-fluorometer， use the 1933 Solid-SampleHolder (Fig. 4) at a 30°or 60° angle forsolids. For liquids， use the 1967 Front-Face Thermostatted Cell Holder withmagnetic stirrer accessory. Fig. 4. 1933 Solid-Sample Holder accessorywith sample block. Copyright C HORIBA Jobin Yvon； version .HORIBAExplore the future HORIBAJOBIN YVONChina： +() ORIBAExplore the future For our Fluorolog® modular spectrofluorometer, use the 22.5° collectionpath for liquid and solid samples. For our bench-top FluoroMax® spectrofluorometer, use the 1933 Solid-Sample Holder (Fig. 4) at a 30° or 60° angle for solids. For liquids, use the 1967 Front-Face Thermostatted Cell Holder with magnetic stirrer accessory.