Different methods of target DNA detection has been used using FRET QNZ price phenomena. Most of these methods are based on the hybridization between target DNA and QD-tagged probes (QD nanoprobes). These probes are usually double-tagged with QD (in one end) as well as a quencher molecule (in the other end). As mentioned previously, these nanoprobes can be designed to produce signal (signal on) or disappear the signal of tagged QD molecule (signal off) when they recognize target DNA. In the signal-on method the probe

DNA is designed as stem-loop structure. In this state QD is located in the vicinity of quencher molecule, absorbing the fluorescent signal of QD and preventing it from detection. However, when the nanoprobe hybridizes with the target DNA, the stem-loop structure denatures and is converted to the linear conformation. The QD and quencher molecule are thus located away from each other, making it possible to detect the fluorescent signal of tagged QD. In the signal-off method, the nanoprobe is tagged with QD and the target selleck compound is tagged with quencher. In unhybridized state, the tagged QD emits signal and its

signal is detectable. But when the nanoprobe recognizes the target DNA, it hybridizes the target DNA, leading to bringing QD to the vicinity of quencher and prevention of QD emission [52]. QDs can also be used as electroactive labels for detection

of target DNA in the electrochemical biosensors. This property originates from inherent electrochemical properties with ease of miniaturization, low cost, low power requirements, and excellent biocompatibility. In electrochemical detection of target DNA molecules by QDs, they serve as electrochemical catalyst (electroactive molecules), which transports loads of electrons through the reduction of dissolved oxygen, resulting in a significant increase in the reduction peak current. In fact, they show sharp selleck kinase inhibitor voltammetry signals proportional to the concentration of corresponding DNA targets and serve as signal-enhancing agents [53]. In addition to detection of one target, several different-sized Mirabegron QD molecules can be excited by one excitation source simultaneously. This ability is advantageous in detecting more than one target in the same time [54]. It is thus possible to implement multiplex iLAMP assays for detecting multiple proteins in a sample. The application of nanoprobes for detecting iLAMP products is depicted in Figure 2. Figure 2 The principle and possible ways of iLAMP products analysis with different nanoprobes (nanoprobe-iLAMP platform). Integration with liposome Liposomes are spherical micro/nanostructures made of lipid bilayers and can be filled with various molecules.