Multiplexed Probe Sets
Multiplexed Probe Sets - Related Videos
10:15
Multiplex PCR and Reverse Line Blot Hybridization Assay (mPCR/RLB)
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Cited by 21 •
2011
An inexpensive, high throughput method for simultaneous detection of up to 43 molecular targets is described. Applications of mPCR/RLB include microbial typing and detection of multiple pathogens from clinical samples.
13:14
Genetic Barcoding with Fluorescent Proteins for Multiplexed Applications
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Cited by 4 •
2015
Since the discovery of the green fluorescent protein gene, fluorescent proteins have impacted molecular cell biology. This protocol describes how expression of distinct fluorescent proteins through genetic engineering is used for barcoding individual cells. The procedure enables tracking distinct populations in a cell mixture, which is ideal for multiplexed applications.
05:22
A Multiplex Serological Assay for the Detection of Antibody Responses to Arboviruses
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2025
Multiplex fluorescence immunoassays are becoming a reference for serology testing. Their application, however, is limited by the complexity and time-consuming bead-analyte coupling processes. This report presents a semi-automated, reproducible multiplex microsphere bead coupling protocol that is comparable to the standard method while considerably reducing time to results.
08:05
Multiplexed Fluorometric ImmunoAssay Testing Methodology and Troubleshooting
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Cited by 19 •
2011
Using Luminex Corporation’s xMAP microsphere technology, we have developed the Multiplexed Fluorometric ImmunoAssay (MFIA) for serosurveillance of various laboratory animal species. The MFIA is a suspension microarray where antigen, tissue control or immunoglobulins are covalently linked to color-coded polystyrene microspheres. The MFIA testing method as well as various troubleshooting topics is addressed.
08:43
Highly Multiplexed, Super-resolution Imaging of T Cells Using madSTORM
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Cited by 5 •
2017
We demonstrate a method to image multiple molecules within heterogeneous nano-structures at single molecule accuracy using sequential binding and elution of fluorescently labeled antibodies.
FAQs
Each probe is designed to hybridize with a different RNA or DNA sequence. The resulting target-specific signals are then distinguished through unique fluorescent labels, molecular barcodes, or combinations of signals. This encoding lets researchers assign observed signals to particular transcripts while examining multiple molecular features within the same cell or tissue section.
These identifiers provide the readout needed to separate overlapping measurements. Rather than treating all probe binding as one signal, researchers can associate each color, barcode, or signal combination with a particular target. That distinction supports simultaneous analysis of several transcripts and makes complex molecular patterns interpretable in spatially organized neural samples.
Spatial context shows where a molecular signature occurs within a cell or tissue section. Researchers can therefore relate transcript patterns to cell identity, anatomy, and the organization of neuronal or glial populations. This adds positional information to gene-expression profiling, helping connect molecular observations with the structure of brain tissue.
The selected probe sequences determine which RNA or DNA targets are represented in the measurement. A set focused on several transcripts can reveal molecular signatures, whereas targets chosen across neuronal or glial populations can support comparisons among cell types. Thus, probe-set composition links the assay directly to the biological questions being examined.
At a high level, researchers apply a collection of sequence-specific probes to cells or a tissue section, allow each probe to hybridize with its corresponding RNA or DNA sequence, and distinguish the resulting signals through labels, barcodes, or signal combinations. The detected pattern can then be examined for transcript distribution and cellular or anatomical relationships.
They are useful when a study must examine several molecular targets while preserving their locations in neural tissue. Applications include multiplexed in situ hybridization, gene-expression profiling, and spatial mapping of neuronal and glial populations. These uses help researchers investigate brain organization and function without separating each target into an entirely different spatial analysis.
The combined signal pattern can identify molecular signatures associated with neuronal or glial populations and show where those signatures occur. Researchers can use this information to relate cell identity to anatomy and connectivity, or to examine disease-associated changes. The outcome is a spatially resolved view of how molecular features are organized across brain tissue.