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Multiplex cell microarrays for high-throughput screening

delete2016-01-01
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PRE
AI
O
Ophélie I. Berthuy
S
Sinan Muldur
F
François Rossi
P
Pascal Colpo
L
Loı̈c J. Blum
C
Christophe A. Marquette *
DOI:10.1039/c6lc00831cdelete
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Abstract

Abstract

En 中文
Microarray technology was developed in the early 1990s to measure the transcription levels of thousands of genes in parallel. The basic premise of high-density arraying has since been expanded to create cell microarrays. Cells on chip are powerful experimental tools for high-throughput and multiplex screening of samples or cellular functions. Miniaturization increases assay throughput while reducing both reagent consumption and cell population heterogeneity effect, making these systems attractive for a wide range of assays, from drug discovery to toxicology, stem cell research and therapy. It is usual to functionalize the surface of a substrate to design cell microarrays. One form of cell microarrays, the transfected cell microarray, wherein plasmid DNA or siRNA spotted on the surface of a substrate is reverse-transfected locally into adherent cells, has become a standard tool for parallel cell-based analysis. With the advent of technology, cells can also be directly spotted onto functionalized surfaces using robotic fluid-dispensing devices or printed directly on bio-ink material. We are providing herein an overview of the latest developments in optical cell microarrays allowing high-throughput and high-content analysis.
Keywords:
SECRETED ALKALINE-PHOSPHATASE
GENE-EXPRESSION
ELECTROCHEMICAL DETECTION
PLASMA POLYMERIZATION
ON-CHIP
SURFACE FUNCTIONALIZATION
CYTOMETRY PLATFORM
SINGLE CELLS
STEM
PROTEIN
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Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.

Journal

L
Lab on a Chip
IF:
5.4
Papers:
9.0K
Citations:
3.3W

Organization

C
centre national de la recherche scientifique (cnrs)
Scholars:
24.5W
Papers: 18.2W
Citations: 279
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