Figure 7.
Recommendations for DNA quantitation by SYBR Gold fluorescence. (A) Phase diagram depicting different regimes of DNA detection by SYBR Gold fluorescence, as a function of SYBR Gold and DNA concentrations. (B) Fluorescence intensity recorded using a qPCR cycler at constant DNA concentration (Lambda DNA, 2.7 μM bp) at varying SYBR Gold concentrations. The data points are the mean values of two independent experiments including their standard deviations or stem from just one experiment. (C) Fluorescence intensity recorded using a plate reader as a function of the dye per base ratio. The circles and error bars are the mean and standard deviation from at least two independent measurements. The SYBR Gold concentrations are (from blue to orange) 0.124, 0.62, 0.83, 1.24, 2.48 μM. These are the same data as in Figure 5D plotted as a function of dyes per bp. (D) Fluorescence intensity recorded using a plate reader as a function of the dye per base ratio. The circles and error bars are the mean and standard deviation from at least two independent measurements. The DNA base pair concentrations are (from dark to light brown) 0.07, 0.13, 0.26, 0.66, 1.3, 2, 2.7 μM.

Recommendations for DNA quantitation by SYBR Gold fluorescence. (A) Phase diagram depicting different regimes of DNA detection by SYBR Gold fluorescence, as a function of SYBR Gold and DNA concentrations. (B) Fluorescence intensity recorded using a qPCR cycler at constant DNA concentration (Lambda DNA, 2.7 μM bp) at varying SYBR Gold concentrations. The data points are the mean values of two independent experiments including their standard deviations or stem from just one experiment. (C) Fluorescence intensity recorded using a plate reader as a function of the dye per base ratio. The circles and error bars are the mean and standard deviation from at least two independent measurements. The SYBR Gold concentrations are (from blue to orange) 0.124, 0.62, 0.83, 1.24, 2.48 μM. These are the same data as in Figure 5D plotted as a function of dyes per bp. (D) Fluorescence intensity recorded using a plate reader as a function of the dye per base ratio. The circles and error bars are the mean and standard deviation from at least two independent measurements. The DNA base pair concentrations are (from dark to light brown) 0.07, 0.13, 0.26, 0.66, 1.3, 2, 2.7 μM.

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