CRG/UPF FACS Unit

CRG/UPF FACS Unit

CRG/UPF FACS Unit

Head of unit
j

CRG/UPF FACS Unit

Head of unit
j

Overview

Flow cytometry studies optical parameters emitted by particles (cells, cell fractions). Flow cytometers can study a series of parameters of individual particles simultaneously, quickly and on a large number of individualized particles in suspension. Flow cytometers use lasers as a source of light excitement; therefore, it must be possible to mark the particles with one or more fluorescent substances. Information is also collected regarding the size and structural complexity of each particle. This multiparameter study of each particle enables us to analyse subpopulations in complex samples through electronic sorting. Some cytometers are also equipped with sorting and collection modules for particles of interest.

The most important applications of flow cytometry include those relating to the study of cell surface receptors, nuclear and cytoplasmic antigens, DNA content, enzyme activity, cell integrity and membrane permeability and calcium flows.

The Unit currently hosts five analyzers and two sorters, and is therewith the largest Becton Dickinson site in Spain. The sorters are operated by the facility personnel, who also support the users in experimental design and data analysis. The analyzers are operated by the users themselves, after they have been trained. The facility personnel helps with the experimental design and supervises and monitors the experiments when necessary.

For further information, please contact Òscar Fornas.

Latest Updates

New technology acquisition:

New SP6800 Spectral Analyzer (Sony Biotechnology) has been acquired to cover advanced multicolour flow cytometry assays. This new technology facilitates the access to complex phenotype analysis while managing up to 34 fluorescences at the same time. Also simplifies the access to complex multicolor panel by eliminating conventional filters and compensation.

References:
https://www.sonybiotechnology.com/us/instruments/sp6800
https://www.ncbi.nlm.nih.gov/pubmed/28518119
https://www.ncbi.nlm.nih.gov/pubmed/27500930

Implemented applications: 

Flow Karyotyping for chromosome sorting was implemented in our facility to isolate chromosomes for chromosome sequencing. Additionally, this methodology allows the detection of numerical and structural chromosome aberrations. Chromosomes of a single type can be purified facilitating gene mapping or production of chromosome-specific recombinant DNA libraries.

Referencehttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753228/

Single Virus Sorting has been developed in our facility to isolate single virus. Single virus isolation allows the access to genome of single virus for sequencing. Single Virus Genomics enable the discovery of some of the likely most abundant and ecologically relevant marine viral species. The method could be used to study other biological entities into different ecosystems.

Reference
Francisco Martinez-Hernandez, Oscar Fornas, Monica Lluesma Gomez, Benjamin Bolduc, Maria Jose de la Cruz Peña, Joaquín Martínez Martínez, Josefa Anton, Josep M. Gasol, Riccardo Rosselli, Francisco Rodriguez-Valera, Matthew B. Sullivan, Silvia G. Acinas & Manuel Martinez-Garcia.
"Single-virus genomics reveals hidden cosmopolitan and abundant viruses"
Nature Communications, 8:15892 (2017)
http://www.nature.com/articles/ncomms15892

Òscar Fornas CV

1996 PhD in Biochemistry at the Autonomous University of Barcelona (UAB), Barcelona, Spain.
1996-2000 Postdoc at Oncologic Research Institute (IRO), Barcelona, Spain.
2000-2001 PI at IDIBAPS, Barcelona, Spain.
2001-2010 Head of Flow Cytometry Core Facility at Pompeu Fabra University (UPF), Barcelona, Spain.
Since March 2010 Head of Flow Cytometry Core Facility at UPF/CRG, Barcelona, Spain.

 

 

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