Microarray Technique
Microarray Technique - Related Videos
03:31
A Technique to Detect Cyanobacterial Strains Using an Antibody Microarray Chip
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2025
This video demonstrates a method to detect the Cyanobacterial strains in an environmental sample using an antibody microarray chip. Samples carrying various bacteria interact with printed antibodies, and immunostaining with fluorophore-labeled anti-cyanobacterial-strain antibodies reveals the presence of specific cyanobacterial strains through fluorescence in distinct spots.
08:29
Expression Profiling with Microarrays
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2023
Microarrays are important tools for profiling gene expression, and are based on complementary binding between probes that are attached to glass chips and nucleic acids derived from samples. Using these arrays, scientists can simultaneously evaluate the expression of thousands of genes. In addition, the expression profiles of different cells or tissue types can be compared, allowing researchers to deduce how the expression of different genes change during biological processes, and thus gain...
03:02
Antibody Microarray: A Technique to Study the Protein Expression of miRNA Treated Lung Cancer Cells
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2023
This video describes the technique to study the protein expression in miRNA transfected lung cancer cells by using antibody microarray to measure specific gene expression. In the featured protocol, we perform antibody microarray for the identification of the activity of a combinatorial miRNA treatment in halting cell cycle and angiogenesis.
13:37
Polymer Microarrays for High Throughput Discovery of Biomaterials
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Cited by 32 •
2012
A description of the formation of a polymer microarray using an on-chip photopolymerization technique. The high throughput surface characterization using atomic force microscopy, water contact angle measurements, X-ray photoelectron spectroscopy and time of flight secondary ion mass spectrometry and a cell attachment assay is also described.
07:04
Performing Custom MicroRNA Microarray Experiments
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Cited by 8 •
2011
A simple procedure of performing custom microRNA microarray experiments is described. The steps include isolating RNA, labeling RNA and reference DNA, hybridizing the samples to microarrays, scanning the microarrays, quantifying and analyzing hybridization signals.
FAQs
Probe–target hybridization provides the specificity that lets a microarray distinguish selected nucleic acid sequences. Known DNA probes are fixed at defined locations, and complementary DNA or RNA in the labeled sample binds there. Fluorescent detection then links signal at each location to the presence of the corresponding target, allowing many targets to be assessed in one experiment.
Fluorescence signal intensity indicates the relative amount of a target associated with a probe, so researchers can compare abundance patterns across biological samples. Stronger or weaker signals are interpreted at the corresponding probe locations rather than as a simple whole-array value. This makes the technique useful for identifying coordinated changes in many targets during sample comparisons.
Microarrays are optimized for efficient, standardized measurements across a defined collection of genes or variants, whereas sequencing offers broader resolution. The choice therefore depends on whether the study prioritizes a consistent, targeted panel or more expansive sequence information. For repeated comparisons using the same selected targets, the microarray format can provide a practical analytical design.
Probe location and sequence determine which nucleic acid target contributes to a measured signal. Because the array contains known DNA probes, researchers can organize readouts around selected genes or variants rather than treating the sample as an undifferentiated mixture. This design supports sequence-specific presence measurements as well as abundance comparisons, depending on the biological question.
A basic workflow begins with an array carrying immobilized probes, followed by application of fluorescently labeled sample DNA or RNA. After complementary sequences hybridize to matching probes, fluorescence is detected at the probe locations. The resulting pattern of signals is then compared across samples or targets to evaluate relative abundance or sequence-specific presence.
For gene-expression studies, researchers compare signal patterns from biological samples to determine which selected genes show different relative abundance. The method can also help classify disease-related sample patterns when the array includes relevant targets. These applications turn many individual probe measurements into a profile that supports comparison among biological states using a defined set of nucleic-acid features.
Genotyping applications focus on whether sample nucleic acids produce signals at probes representing selected variants. A signal pattern can therefore distinguish samples according to sequence-specific presence across the tested set. This approach is useful when the biological question concerns known variants rather than broad sequence discovery, matching the technique’s targeted design.
In studies of environmental or experimental conditions, microarrays can reveal coordinated changes in cellular responses by comparing profiles between treated or otherwise differing samples. The outcome is a pattern of relative signal changes across selected targets, which helps connect a condition with altered gene activity or other measured nucleic-acid features. Interpretation remains tied to the probes included.