Related Experiment Video
Updated: Jul 23, 2026

09:16
Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
Published on: February 21, 2015
Universal labeling chemistry for nucleic acid detection on DNA-arrays
E Bernal-Méndez1, C Tora, I Sothier
1BioMérieux, Advanced Technology, Marcy l'Etoile, France. eloy.bernalmendez@eu.biomerieux.com
Nucleosides, Nucleotides & Nucleic Acids
|October 21, 2003
Summary
Researchers developed a novel aqueous chemistry for labeling nucleic acids, enabling detection on DNA chips. This method uses a diazo group for selective phosphate labeling and biotin for detection without affecting hybridization.
Area of Science:
- Biochemistry
- Molecular Biology
- Analytical Chemistry
Background:
- Nucleic acid detection is crucial for molecular diagnostics and research.
- Current labeling methods may face limitations in efficiency or specificity.
- DNA chips offer a platform for high-throughput nucleic acid analysis.
Purpose of the Study:
- To develop a new, efficient aqueous chemistry for labeling any class of nucleic acids.
- To enable sensitive detection of labeled nucleic acids on DNA chips.
- To ensure the labeling chemistry preserves nucleic acid hybridization specificity.
Main Methods:
- A novel aqueous labeling chemistry was designed.
- The chemistry utilizes a diazo function as the reactive moiety.
- Biotin was incorporated as the detectable unit.
Main Results:
- The developed chemistry efficiently labels various nucleic acids in an aqueous environment.
- The diazo group selectively reacts with the phosphate backbone.
- Labeling did not interfere with base pairing or hybridization specificity on DNA chips.
Conclusions:
- This new aqueous chemistry provides an efficient and selective method for nucleic acid labeling.
- The method is suitable for detecting nucleic acids on DNA chips.
- The preservation of hybridization specificity is a key advantage for diagnostic applications.
Related Concept Videos
Labeling DNA Probes
DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Southern Blot
Agarose gel electrophoresis is very useful in separating DNA fragments by size. Running a DNA ladder containing fragments of the known length alongside the sample helps determine the approximate length of the sample DNA fragments. However, additional steps are needed to verify the sequence identity of the sample DNA fragments.
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
DNA Microarrays
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
Sanger Sequencing
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
In-situ Hybridization
In situ hybridization (ISH) is a technique used to detect and localize specific DNA or RNA molecules in cells, tissue, or tissue sections using a labeled probe. The technique was first used in 1969 for the investigation of nucleic acids. It is currently an essential tool in scientific research and clinical settings, especially for diagnostic purposes.
Types of probes and labels
A probe is a complementary strand of DNA or RNA that binds to corresponding nucleotide sequences in a cell. Many...
Types of probes and labels
A probe is a complementary strand of DNA or RNA that binds to corresponding nucleotide sequences in a cell. Many...

