Long Stokes
Long stokes To address this shortcoming, we developed a long Stokes shift RFP-based Ca(2+) indicator, REX-GECO1, with optimal two-photon excitation at REX-GECO1 fluoresces at nm when excited at nm or nm by a one- or two-photon process, [HOST] by:
DyLight Long Stokes Shift Dyes can be used individually or combined with DyLight for multiplexed analysis. The excitation and emission peaks are sufficiently separated so as to minimize dye-dye quenching in assays. Single excitation wavelength –DyLight Long Stokes Shift Dyes all can be excited together at nm using an Argon laser. Image.
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Oct 31, · To address this shortcoming, we developed a long Stokes shift RFP-based Ca2+ indicator, REX-GECO1, with optimal two-photon excitation at Cited by:
Thermo Scientific DyLight Long Stokes Shift Specialty Dyes have fluorescence emission from green to far red with a single excitation peak that matches the laser line and very large Stokes shifts that inhibit quenching.
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A transient ischemic attack (TIA) is sometimes called a “mini-stroke.” It is different from the major types of stroke because blood flow to the brain is blocked for only a short time—usually no more than 5 minutes. 2 It is important to know that.
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The Thermo Scientific DyLight Long Stokes Shift Dyes are amine-reactive fluorescent dyes that produce long Stokes (LS) shifts of nm in excitation/emission wavelengths (see Table 1). The DyLight LS Dyes provide multicolor detection.
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Abberior STAR SX is the dye of choice for long Stokes STED applications in the orange fluorescent regime. The dye is particularly designed and tested for 2-color STED microscopy in combination with our STAR using a single STED wavelength. The dye is our recommendation for usage in the Leica TCS STED Ti:Sa 2-color system. Key Features.
Long Stokes-Shift The common characteristic of the dyes is an exceptional long Stokes-shift between the excitation and emission maximum. Our abberior STAR SXP dyes are designed to provide bright fluorescence for multiplexed imaging.
Feb 27, · Long Stokes shift fluorescence of fluorescent proteins occurs when the pK a of the neutral phenol form of the chromophore substantially decreases upon excitation, leading to excited state proton transfer (ESPT) and emission of fluorescence from the anionic phenolate form. As the phenol form is higher energy than the phenolate form, the energy difference between excitation and emission Cited by:
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