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Luminex Life Science Assays



About xMAP Technology

Luminex’s xMAP technology is built on proven, existing technology that have been combined in a unique way. Featuring a flexible, open-architecture design, xMAP technology can be configured to perform a wide variety of bioassays quickly, cost-effectively and accurately.

 

 

The Luminex reader combines two lasers, fluidics, and real-time digital signal processing to distinguish up to 100 different sets of color-coded polystyrene beads, each bearing a different assay. The Luminex reader is an essential tool that performs the key functions of this multiplex technology.

 


Fluidics
— The reader detects individual beads by flow cytometry. The fluidics system of the reader aligns the beads into single file as they enter a stream of sheath fluid and then enter a flow cell. Once the beads are in single file within the flow cell, each bead is individually interrogated for bead color (analyte) and assay signal strength (PE fluorescence intensity).

 

Lasers — The reader uses a 532 nm green laser (“assay” laser) is used to excite the PE dye of

the assay (Streptavidin-PE). The 635 nm solid state laser (red “classify” laser) is used to excite

the dyes inside the beads to determine their “color” or “region” and is also used for doublet

discrimination by light scatter

 

Detectors — The reader has four detectors, one for each of the optical paths shown in the figure below. Detectors are used to measure the fluorescence of the assay, to make bead determination (1-100) and the last to discriminate between single and aggregate beads.

 

 




How xMAP Technology Works
 
Luminex uses proprietary techniques to  internally color-code microspheres with two fluorescent dyes. Through precise concentrations of these dyes, 100 distinctly colored bead sets can be created, each of which can be coated with a reagent specific to a particular bioassay. Reagents may include antigens, antibodies, oligonucleotides, enzyme substrates, or receptors.




An analyte from a test sample is captured by the bead, a reporter molecule, labeled with a different fluorescent dye, is introduced to complete the reaction on the surface of each microsphere.



 

 

The microspheres pass rapidly through a laser, which excites the internal dyes marking the microsphere set. A second laser excites the fluorescent dye on the reporter molecule.
 
High-speed digital-signal processors identify each individual microsphere and quantify the result of its bioassay, based on fluorescent reporter signals.






High-throughput Multiplex Bead Based Assays
 
Panomics has an aggressive program for the development of a broad range of assays for the Luminex platform and similar instruments based on the xMAP technology.
Panomics is also proud to be one of the few Luminex Certified Developers. Luminex have recognized Panomics as having both unique and extensive assay development capabilities.
 
Gene Expression: Quantitatively measure up to 36 different RNA transcripts directly from sample source with unparalleled accuracy and precision.
Transcription Factor: Quantitate the DNA binding activity of up to 44 different TFs in a sinlge well using nuclear extract or whole cell lysates.
Cytokine/Chemokines: Quantitatively measure 3-30 cytokines simultaneously from a variety of matrices including cell culture supernatants, serum, plasma, cell/tissue lysates and bodily fluids.
SH2 Domain: Profile phosphotyrosine protein interactions against 30 SH2 in a single well using treated and untreated cell lysates.

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Protein DNA
Electrophoresis
Gene Expression
Cytokines
Fluorochromes
Precast Gel

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