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Kroneis, T; Chen, S; El-Heliebi, A.
Low-Volume On-Chip Single-Cell Whole Genome Amplification for Multiple Subsequent Analyses.
Methods Mol Biol. 2015; 1347(22):245-261 Doi: 10.1007/978-1-4939-2990-0_17
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Führende Autor*innen der Med Uni Graz
Kroneis Thomas
Co-Autor*innen der Med Uni Graz
Chen Shukun
El-Heliebi Amin
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Abstract:
Multiple analyses such as DNA profiling, sequencing, or comparative genome hybridization (CGH) done on the single-cell level long for pre-amplification due to the diploid human genome. Isothermal whole genome amplification allows amplification of long DNA templates from single cells. When analysis needs to be performed under rare cell conditions additional care needs to be taken due to the fact that, even after pre-enrichment, few candidate target cells are still dispersed among an overwhelming number of non-target background cells. Here, we describe a protocol where we define a population of candidate target cells based on specific staining. Candidate cells are then isolated by laser microdissection and pressure catapulting (LMPC) and transferred onto a microliter reaction slide. This slide allows monitoring the single-cell isolation process and isothermal whole genome amplification in less than 2 μL. The amplification products obtained from single cells can be forwarded to multiple analyses.
Find related publications in this database (using NLM MeSH Indexing)
Genome -
Genomics - methods
Immunohistochemistry -
Laser Capture Microdissection -
Microfluidic Analytical Techniques -
Nucleic Acid Amplification Techniques -
Single-Cell Analysis - methods

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