A fluorometer typically consists of a light source, a sample chamber, and a detector. The light source is used to excite the fluorescent molecules in the sample. The excited molecules then emit light of a different wavelength, which is detected by the detector. The intensity of the emitted light is proportional to the concentration of fluorescent molecules in the sample. This allows fluorometers to be used for quantitative measurements. It can be selective for specific fluorescent molecules, which makes it useful for identifying and quantifying specific compounds in a mixture and measurements can be made quickly and easily.
Dynamic range : Five orders of magnitude
Linear dynamic range : R2 >0.995
Processing time : 3s (Once)
Light source : UV LED Blue LED
Dynamic range : Five orders of magnitude
Linear dynamic range : R2 >0.995
Processing time : 3s (Once)
Light source : Blue LED Red LED
Dynamic range : Five orders of magnitude
Linear dynamic range : R2 >0.995
Processing time : 3s (Once)
Light source : Blue LED Green LED