Welcome in INRA - GABI

Welcome in INRA - GABI
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ICE (Iso Cell Express): an integrated solution for microgenomics

INRA ICE Integrated Microgenomics platform
© INRA ICE
At ICE, we have solid experience in the field of "Integrative Microgenomics", combining Laser Capture Microdissection (LCM) and Expressional Genomics (transcriptomics and proteomics). Our team, made up of experienced experts in this innovating field, provides access to cutting edge technology for your analyses.
 
One of today's challenges for biologists is the ability to understand and analyse the genome expressed by a particular cell type. This means working on very small or even tiny quantities of biological material.
 
ICE is an open structure working mainly at a local and regional level, supported by the research team "Milk, Genome and Health" or LGS of the joint research unit GABI (Animal Genetics and Integrative Biology) involved in programs for the analysis of gene expression.
 
The originality of the ICE platform relies on its capacity to produce and analyse microquantities of material extracted from cells isolated from their tissular environment, under morphological control, using laser microdissection.
 
Microgenomics requires highly specialised equipment and an expertise for handling very small amounts of biological material.

Our staff with expertise in transcriptomics and proteomics makes it possible to offer access to high level support, a customized offer to match your specific needs in integrated solutions in microgenomics and individual services for the differential analysis of biomolecules, in close interaction with the other platforms at Jouy-en-Josas (PAPSSO i.e. platform for proteomic analyses, CRB-GADIE and MIMA2 i.e. platform for microscopy and imaging analyses of micro-organisms, animals and foods). T
his localization provides a specific environment, enabling the platform to work on improving necessary technology that is then made available to its users.

 
The objectives of the platform are:
 
  • Hosting, providing council and accompanying users to develop, perform and interpret genetic expression analyses, on both the tissular and cellular levels using high-performance technology
  • Providing theoretical and pratical training for the technologies that are offered by the platform
  • Monitoring technological surveillance and providing tested and validated methods
 
Our specificities: 
 

1 - Laser microdissection: capturing and/or cutting (LCM)


« Laser capture microdissection » is based on the use of an IR laser (low energy) that permits cell capture by adhering the cells to a film. This technology is particularly adapted to the isolation of single cells (or epithelia), therefore preserving the integrity of the extracted biomolecules, in particular RNA.
 
« Laser cutting microdissection » is based on the use of a UV laser that ablates the tissue surrounding the targeted region, which is then retrieved for further analysis. This technique is particularly well adapted to the isolation of large pieces of tissueresistant tissues or chromosomes.
 
The ICE platform is equipped with the VERITAS microdissector (Arcturus, Molecular Device), which permits both capture and cutting of samples. This unique combination is therefore adapted to a larger number of applications.

Before beginning a project, a "feasibility test" is performed in order to check that the tissue sample is compatible with laser microdissection, to decide on which technology should be used (capture and/or cutting) and to define which procedures will be performed for the analysis of the biomolecules. The sample's quantity and quality are also verified.  Then users are quickly informed on their demand is feasible or not.
 

2 - Real Time Quantitative PCR and TLDA


The ICE platform has an ABI Prism 7900 HT (Applied Biosystems) equipped with a standard 96-well block and a block adapted to
TLDA (TaqMan Low Density Array) microfluidic chips, precharged (TaqMan primers and probes specific for important genes). These microarrays permit simultaneous analysis of the expression of 16 to 384 genes. (For more information, please consult the Applied Biosystems website). 
 

3 - Expressionnal Microgenomics


ICE has optimised its methods for the molecular study of cells and offers an overall package integrating the preparation of histological cuts, microdissection, biomolecule extraction, quality control and differential analysis of proteins (2D-DIGE, marking with saturation) and/or on transcripts (simple qPCR or TLDA, or after microarray amplification).
 
The staff on the platform may accompany users in the development of their qPCR project including the analysis of the results.
 

Equipment


  • Laser Microdissection:
- Sample preparation: liquid nitrogen cryogrinder, Nanodrop (Nixor Biotech), Bioanalyser 2100 (Agilent)
- Laser Microdissection (LCM): Cryostat (Thermo), Veritas (Arcturus, Molecular Devices)
 
  • Electrophoresis:
- 2D-DIGE electrophoresis system
- Automatic cutting of spots: EXQuest spot cutter (Bio-Rad)
- Scanners and imaging for data acquisition: Typhoon (GE-Healthcare)
 

Services


  • Histological cuts
  • Laser capture microdissection (LCM)
  • RNA and protein quality control and quantification 
  • 2D Gel separation of proteins: 2D-DIGE
  • Quantification and qualification of microquantities of proteins
 

BILLING


ICE defines its own billing conditions as flat rates or individual services. The costs include the prices established by similar Shared Experimental Facilities (DEP) outside of INRA. Our prices are guaranteed for one calendar year.
 

DELAYS


ICE guarantees a response to all  requests within eight days. An estimate will then be made indicating the exact nature of the service(s) provided, their cost and the delays.
 

Contacts


INRA JOUY-EN-JOSAS Center - Building 221 – Lait Génome et Santé (for the Milk Genome and Health team)
Domaine de Vilvert, 78352 Jouy- en-Josas cedex

> Patrice Martin, Scientific director of the platform; email: patrice.martin@jouy.inra.fr
> Claudia Bevilacqua, Operational manager of the platform; email: claudia.bevilacqua@jouy.inra.fr                                               
Writing: P. Martin - Edition P. Huan - Translation W. Brand-Williams and H. Hayes
Creation date: 12 April 2010
Update: 26 March 2013