By taking advantage of the large signal amplification through efficient fluorescence resonance energy transfer (FRET) from the conjugated polymer to the intercalating dye mediated by DNA, a new strategy for nuclease assay has been developed using conjugated polymer and DNA/intercalating dye complex. The discrimination of DNA before or after digestion by nuclease denotes the universal application of the approach, in which either dsDNA or ssDNA substrates could be used for detecting nuclease activity. This method can be extended to most nucleases by simply changing the Substrate DNA. The present method is label-free, rapid,and highly sensitive, with a detection limit Much better or at least comparable to previous reports. fit addition, this a...
Visual DNA amplification using a simple polymerase chain reaction (PCR) device is useful for field t...
In this paper, a simple and rapid method was developed for real-time monitoring of the kinetics of d...
In this study, we developed an innovative highly specific nucleic acid isothermal detection assay ba...
Here we report on the development of an antibody-modified nucleotide and its sequence-selective inco...
We show that nucleotides which are modified with a G-quadruplex-derived DNAzyme are substrates for D...
The research presented in this thesis introduces design criteria for development of a new type of se...
We developed a versatile DNA assay and framework for monitoring polymerization of DNA in real time a...
This is the final version. Available from Springer Nature via the DOI in this record.DNA and RNA nuc...
A label-free complex probe composed of a water-soluble fluorescent pyrene-functionalized polymer, ss...
A facile and general label-free assay for sensitive and selective DNA detection has been developed b...
In this article, we report on the first use of fluorescence resonance energy transfer (FRET) dye-lab...
Sensitive detection assays are a prerequisite for the analysis of small amounts of samples derived f...
An alternative fluorescence-based method has been developed for the direct detection of small quanti...
We have developed a new sensing system based on quantitative real-time polymerase chain reaction ass...
Nucleolytic enzymes are associated with various diseases, and several methods have been developed fo...
Visual DNA amplification using a simple polymerase chain reaction (PCR) device is useful for field t...
In this paper, a simple and rapid method was developed for real-time monitoring of the kinetics of d...
In this study, we developed an innovative highly specific nucleic acid isothermal detection assay ba...
Here we report on the development of an antibody-modified nucleotide and its sequence-selective inco...
We show that nucleotides which are modified with a G-quadruplex-derived DNAzyme are substrates for D...
The research presented in this thesis introduces design criteria for development of a new type of se...
We developed a versatile DNA assay and framework for monitoring polymerization of DNA in real time a...
This is the final version. Available from Springer Nature via the DOI in this record.DNA and RNA nuc...
A label-free complex probe composed of a water-soluble fluorescent pyrene-functionalized polymer, ss...
A facile and general label-free assay for sensitive and selective DNA detection has been developed b...
In this article, we report on the first use of fluorescence resonance energy transfer (FRET) dye-lab...
Sensitive detection assays are a prerequisite for the analysis of small amounts of samples derived f...
An alternative fluorescence-based method has been developed for the direct detection of small quanti...
We have developed a new sensing system based on quantitative real-time polymerase chain reaction ass...
Nucleolytic enzymes are associated with various diseases, and several methods have been developed fo...
Visual DNA amplification using a simple polymerase chain reaction (PCR) device is useful for field t...
In this paper, a simple and rapid method was developed for real-time monitoring of the kinetics of d...
In this study, we developed an innovative highly specific nucleic acid isothermal detection assay ba...