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Related Concept Videos

DNA Microarrays02:34

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...

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Related Experiment Video

Updated: Jul 19, 2026

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning
09:27

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning

Published on: March 15, 2011

Robust and efficient synthetic method for forming DNA microarrays.

P L Dolan1, Y Wu, L K Ista

  • 1Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.

Nucleic Acids Research
|November 3, 2001
PubMed
Summary

Researchers developed a new DNA microarray method using p-aminophenyl trimethoxysilane (ATMS)/diazotization chemistry. This technique enables sensitive gene expression analysis with reusable slides and improved DNA binding.

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Last Updated: Jul 19, 2026

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning
09:27

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Published on: March 15, 2011

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High-Density DNA and RNA microarrays - Photolithographic Synthesis, Hybridization and Preparation of Large Nucleic Acid Libraries

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Area of Science:

  • Biotechnology
  • Molecular Biology
  • Genomics

Background:

  • DNA microarray technology is crucial for measuring global gene expression patterns.
  • Current methods require interdisciplinary collaboration for efficient gene expression analysis.
  • Improving DNA immobilization on glass slides is key to enhancing microarray performance.

Purpose of the Study:

  • To develop a chemically reactive surface for covalent DNA binding on glass slides.
  • To improve cDNA microarray technology through enhanced DNA immobilization.
  • To create reusable microarrays with sensitive detection capabilities.

Main Methods:

  • Fabrication of microarrays using p-aminophenyl trimethoxysilane (ATMS)/diazotization chemistry.
  • Analysis of DNA spot uniformity and quantity compared to commercial techniques.
  • Hybridization analysis to assess sensitivity and background fluorescence.

Main Results:

  • The ATMS/diazotization method resulted in uniform DNA spots with equivalent or greater DNA amounts than commercial methods.
  • Hybridization analyses demonstrated 2-3 orders of magnitude greater sensitivity for target sequence detection.
  • Minimal DNA loss during repeated stripping and re-hybridization confirmed slide reusability.

Conclusions:

  • ATMS/diazotization chemistry facilitates covalent binding of unmodified DNA to glass slides.
  • The developed reusable microarrays exhibit enhanced hybridization sensitivity and low background fluorescence.
  • This advancement offers a more efficient and sensitive platform for gene expression profiling.