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游离及与蛋白质结合的荧光素染料的荧光特性。I. 宏观光谱荧光测量

Fluorescence properties of free and protein bound fluorescein dyes. I. Macrospectrofluorometric measurements.

作者信息

Schauenstein K, Schauenstein E, Wick G

出版信息

J Histochem Cytochem. 1978 Apr;26(4):277-83. doi: 10.1177/26.4.77868.

Abstract

Excitation and emission properties of fluorescein derivatives were studied macrofluorometrically. Measurements were performed with solutions of various concentrations (0.07-100 microgram/ml) of free sodium fluorescein prepared from fluorescein diacetate (FDA), fluorescein isothiocyanate (FITC) and FITC bound to rabbit gamma-globulin. Both excitation and emission spectra as well as fluorescence intensities at constant excitation/emission wavelengths (496/515 nm) were recorded. The findings indicate that (1) FDA gives about twice the fluorescence intensity compared to equal concentrations of FITC. (2) The fluorescence properties of FITC upon excitation with blue light (lambda = 496 nm) are only slightly altered by the conjugation to rabbit gamma-globulin. (3) Considerable quenching due to conjugation could, however, be shown to occur upon UV excitation (lambda = 340 nm). (4) Fluorescence emission excited by visible blue light (496 nm) increases linearly to dye concentration in a range of 0.07-2.5 microgram/ml. Beginning at 5 microgram/ml (10-(5) M/1) all three compounds show a sharp decrease of fluorescence intensity with further increasing concentration. Practical aspects of these data for the immunofluorescence method are discussed.

摘要

采用宏观荧光测定法研究了荧光素衍生物的激发和发射特性。使用由荧光素二乙酸酯(FDA)、异硫氰酸荧光素(FITC)以及与兔γ球蛋白结合的FITC制备的不同浓度(0.07 - 100微克/毫升)的游离荧光素钠溶液进行测量。记录了激发光谱和发射光谱以及在恒定激发/发射波长(496/515纳米)下的荧光强度。研究结果表明:(1)与等浓度的FITC相比,FDA的荧光强度约为其两倍。(2)蓝光(λ = 496纳米)激发时,FITC与兔γ球蛋白结合后其荧光特性仅略有改变。(3)然而,在紫外激发(λ = 340纳米)时,可显示出由于结合导致的显著淬灭。(4)在0.07 - 2.5微克/毫升范围内,可见光蓝光(496纳米)激发的荧光发射随染料浓度呈线性增加。从5微克/毫升(10⁻⁵摩尔/升)开始,随着浓度进一步增加,所有三种化合物的荧光强度均急剧下降。讨论了这些数据在免疫荧光法中的实际应用。

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