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    ATTA


        Cell Based Assays 2012
                     26th -27th June 2012 London, UK

       Cell Based Assays Conference is a much awaited symposium where latest
       developments on cell based assays and their significance to the strategic
       future of Research and Development in pharmaceutical industry will be
       discussed and debated. Here in Cell Based Assays Conference keynote
       speakers like Eberhard Krausz, Marianthi Papakosta, Marie H. Delmotte,
       Dr. Peter Horvath, Professor Marc Bickle etc will come and provide latest
       updates on cell based assays. Plenary sessions, debates and discussions
       will be very much beneficial


       Who should attend this event?


       Heads of Department, Directors, Managers, Team Leaders Researchers and
       Scientists from:


          Screening
          Pre-clinical Research
          Pharmacology
          Lead discovery technologies
          Molecular and cellular biology
          Biological technologies
          Lead generation and optimization
          High-content analysis
          Target identification and validation
          Target discovery
          In vitro assays
          Compound profiling
          Assay development




1
                                                                       ATTA
Cell Based Assays 2012
                                 26th-27th June 2012, London UK.


Key Speakers
Eberhard Krausz, Director, Assay Development & Target Validation, Enabling Biology, Janssen
Research & Development

Marianthi Papakosta Scientific Director at Grunenthal GmbH

Marie H. Delmotte Lab Head Cellular and Molecular Biology at Novartis

Dr. Jeroen van Bergeijk GPRD Research Neuroscience Molecular Biology & Biochemistry Abbott
GmbH & Co. KG

Dr. Xavier Leroy Project Promoter & Leader Associate Director Drug Discovery Dept. Actelion
Pharmaceuticals Ltd

Thomas Koblizek Senior Scientist R&D Lonza

Dr. Peter Horvath, Head of image and data analysis, ETH Zurich, Light Microscopy Centre.

Marc Bickle Head of Technology Development Studio at Max Planck Institute of Molecular Cell
Biology and Genetics

Remko de Pril Team Leader Target Discovery and High-Content Screening Galapagos

David R. Greaves Professor of Inflammation Biology Sir William Dunn School of Pathology University
of Oxford

Robin Ketteler MRC LMCB University College London

Jens Kelm, PhD, co-founder of InSphero AG




Sponsored by:
InSphero AG          Lonza         TAP Biosystems




Organized by: ATTA LTD. http://www.attaconference.co.uk
Day 1                                               Cell Based Assays 2012
                                             12:00 Sponsor Speaking section th June 2012
                                                                             contact
09:00 Registration and refreshments                                      26
                                             tareef.ahmed@atta-online.co.uk


09:30 Opening address from the Chair         12:40 Networking lunch

09:40 Quantitative analysis of cell-based    13:40 Targeting endogenous stem cells
high-content drug and siRNA screens -        for therapy
How can machine intelligence help?           Targeting endogenous stem cells for
Image quality enhancement (vignetting)       therapy and related approaches (e.g.
Image analysis of end point- and time-       IPSCs).
resolved data (segmentation, feature         Recruitment of (neuronal) stem and
extraction, tracking) Multi-parametric       precursor cells for regeneration &
analysis of single cell-based assays using   neuroprotection
machine learning (classification,            Targeting cancer stem cells for
regression, method optimization, weakly-     oncology
supervised approaches)                       Hedgehog signaling
Statistical analysis and quality control     Dr. Jeroen van Bergeijk GPRD
issues                                       Research Neuroscience Molecular
Dr. Peter Horvath, Head of image and         Biology & Biochemistry Abbott GmbH
data analysis, ETH Zurich, Light             & Co. KG
Microscopy Centre
                                             14:20 Carcinogenicity risk assessment
10:20 Systematic analysis of complex         of Biologics using in vitro cell-based
signal transduction pathways using protein   assays
fragment complementation assays              Marie H. Delmotte Lab Head -
Protein:protein interactions Classical       Cellular and Molecular Biology at
GPCR signaling Non-classical GPCR            Novartis
pathways and interconnectivity Examples
for complex networks The PCA working         15:00 Afternoon Refreshments
principle Some PCA examples
Somatostatin homodimers/heterodimer          15:20 Sponsor Speaking section contact
data CXCR4 agonist/antagonist data           tareef.ahmed@atta-online.co.uk for more
Thomas Koblizek Senior Scientist R&D         detail
Lonza
                                             16:00 Pores for thought; analyses of
11:00 Morning refreshments                   TRPV1 chimeras using a bespoke heat
                                             activation assay, demonstrate that
11:20 Use of cell based GPCR assays to       differences in the pore domain confer
identify novel CB2 agonists and              species specific pharmacological
chemokine receptor antagonists               sensitivity
David R. Greaves Professor of                Marianthi Papakosta Scientific
Inflammation Biology Sir William             Director at Grunenthal GmbH
Dunn School of Pathology University of
Oxford                                       16:40 Closing remarks from the Chair
Day 2                                               Cell Based Assays 2012
                                                                      th
                                                                             27 June 2012

09:00 Registration and refreshments          12:40 Networking lunch

09:30 Opening address from the Chair         13:40 plate based screening
                                             Gene expression assay
09:40 Primary cells and 3D models in         Label-free as well as assay
high-throughput screening                    development native neuronal cell types
Robin Ketteler MRC LMCB University           Presentation from Pfizer
College London
                                             2:00 Sponsor Speaking section contact
10:20 Polarity markers as functional         tareef.ahmed@atta-online.co.uk for more
readouts of hepatic toxicity in 3D           detail
use of bacterial artificial chromosome to
ensure physiological levels of tpj1-cherry   14:20 Beta-Arrestin 2 in Drug
polarity marker expression 3 dimensional     Discovery
cell culture to ensure polarity and          Deorphanisation
functional bile canaliculi system             HTS
generation of transgenic animals for          Biased signaling
primary cell culture high throughput         Scavanger
imaging of live polarised hepatocytes         In-vitro to in-vivo
automated image analysis                      Xavier Leroy, Ph.D. Project Promoter
Marc Bickle Head of Technology               & Leader Associate Director Drug
Development Studio at Max Planck             Discovery Dept. Actelion
Institute of Molecular Cell Biology and      Pharmaceuticals Ltd
Genetics                                     15:00 Afternoon Refreshments

11:00 Morning refreshments                   15:20 Sponsor Speaking section contact
                                             tareef.ahmed@atta-online.co.uk for more
11:20 Application of in vitro 3D models      detail
for drug discovery
More complex and therefore                   16:00 High-Content screen for
physiologically more relevant cell-based     inhibitors of cell migration in cancer
assays will ultimately be more predictive    metastasis using adenoviral knock-
than current 2D-based assays.                down, high-throughput wound healing
Technologies and assay set-up for            assay which we developed to identify
medium-throughput compound screening         novel genes involved in metastatic cell
in 3D (co-) cultures                         migration. Genes whose knock-down
High-content analysis is a versatile         inhibit cell migration were identified
technology platform to capture complex       by their effect on the open wound
cell-based assays.                           Remko de Pril Galapagos Team
Applications in oncology, virology and       Leader Target Discovery and High-
safety pharmacology                          Content Screening
                                             16:40 Closing remarks from the Chair
Eberhard Krausz, Director, Assay
Development & Target Validation,             16:50 End of the conference
Enabling Biology, Janssen Research &
Development, Belgium

12:00 3D Microtissues for Early
Compound De-Risking

Jens Kelm, PhD, co-founder of InSphero
AG
Registration Form for Cell Based Assays 2012
                                              26th -27th June 2012, London UK.




DELEGATE DETAILS
Please complete fully and clearly in capital letters and e-mail it to

tareef.ahmed@atta-online.co.uk


Please photocopy for additional delegates.
Price: £499
Title:
Forename:
Surname:
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Department/Division:
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I agree to be bound by ATTA’s Terms and Conditions of Booking.

 Payment: If payment is not made at the time of booking, then an invoice will be issued and must be paid immediately and
prior to the start of the event. If payment has not been received then credit card details will be requested and payment
taken before entry to the event. Bookings within 7 days of event require payment on booking. Access to the Document
Portal will not be given until payment has been received.
Substitutions/Name Changes: If you are unable to attend you may nominate, in writing, another delegate to take your
place at any time prior to the start of the event. Two or more delegates may not ‘share’ a place at an event. Please make
separate bookings for each delegate.
Cancellation: If you wish to cancel your attendance at an event and you are unable to send a substitute, then we will
refund/credit 50% of the due fee less a £50 administration charge,
providing that cancellation is made in writing and received at least 28 days prior to the start of the event. Regretfully
cancellation after this time cannot be accepted. We will however provide the conferences documentation via the
Document Portal to any delegate who has paid but is unable to attend for any reason. Due to the interactive nature of the
Briefings we are not normally able to provide documentation in these circumstances. We cannot accept cancellations of
orders placed for Documentation or the Document Portal as these are reproduced specifically to order. If we have to
cancel the event for any reason, then we will make a full refund immediately, but disclaim any further liability.
Alterations: It may become necessary for us to make alterations to the content, speakers, timing, venue or date of the
event compared to the advertised programme

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Cell based assays 2012

  • 1. 1 ATTA Cell Based Assays 2012 26th -27th June 2012 London, UK Cell Based Assays Conference is a much awaited symposium where latest developments on cell based assays and their significance to the strategic future of Research and Development in pharmaceutical industry will be discussed and debated. Here in Cell Based Assays Conference keynote speakers like Eberhard Krausz, Marianthi Papakosta, Marie H. Delmotte, Dr. Peter Horvath, Professor Marc Bickle etc will come and provide latest updates on cell based assays. Plenary sessions, debates and discussions will be very much beneficial Who should attend this event? Heads of Department, Directors, Managers, Team Leaders Researchers and Scientists from:  Screening  Pre-clinical Research  Pharmacology  Lead discovery technologies  Molecular and cellular biology  Biological technologies  Lead generation and optimization  High-content analysis  Target identification and validation  Target discovery  In vitro assays  Compound profiling  Assay development 1 ATTA
  • 2. Cell Based Assays 2012 26th-27th June 2012, London UK. Key Speakers Eberhard Krausz, Director, Assay Development & Target Validation, Enabling Biology, Janssen Research & Development Marianthi Papakosta Scientific Director at Grunenthal GmbH Marie H. Delmotte Lab Head Cellular and Molecular Biology at Novartis Dr. Jeroen van Bergeijk GPRD Research Neuroscience Molecular Biology & Biochemistry Abbott GmbH & Co. KG Dr. Xavier Leroy Project Promoter & Leader Associate Director Drug Discovery Dept. Actelion Pharmaceuticals Ltd Thomas Koblizek Senior Scientist R&D Lonza Dr. Peter Horvath, Head of image and data analysis, ETH Zurich, Light Microscopy Centre. Marc Bickle Head of Technology Development Studio at Max Planck Institute of Molecular Cell Biology and Genetics Remko de Pril Team Leader Target Discovery and High-Content Screening Galapagos David R. Greaves Professor of Inflammation Biology Sir William Dunn School of Pathology University of Oxford Robin Ketteler MRC LMCB University College London Jens Kelm, PhD, co-founder of InSphero AG Sponsored by: InSphero AG Lonza TAP Biosystems Organized by: ATTA LTD. http://www.attaconference.co.uk
  • 3. Day 1 Cell Based Assays 2012 12:00 Sponsor Speaking section th June 2012 contact 09:00 Registration and refreshments 26 tareef.ahmed@atta-online.co.uk 09:30 Opening address from the Chair 12:40 Networking lunch 09:40 Quantitative analysis of cell-based 13:40 Targeting endogenous stem cells high-content drug and siRNA screens - for therapy How can machine intelligence help? Targeting endogenous stem cells for Image quality enhancement (vignetting) therapy and related approaches (e.g. Image analysis of end point- and time- IPSCs). resolved data (segmentation, feature Recruitment of (neuronal) stem and extraction, tracking) Multi-parametric precursor cells for regeneration & analysis of single cell-based assays using neuroprotection machine learning (classification, Targeting cancer stem cells for regression, method optimization, weakly- oncology supervised approaches) Hedgehog signaling Statistical analysis and quality control Dr. Jeroen van Bergeijk GPRD issues Research Neuroscience Molecular Dr. Peter Horvath, Head of image and Biology & Biochemistry Abbott GmbH data analysis, ETH Zurich, Light & Co. KG Microscopy Centre 14:20 Carcinogenicity risk assessment 10:20 Systematic analysis of complex of Biologics using in vitro cell-based signal transduction pathways using protein assays fragment complementation assays Marie H. Delmotte Lab Head - Protein:protein interactions Classical Cellular and Molecular Biology at GPCR signaling Non-classical GPCR Novartis pathways and interconnectivity Examples for complex networks The PCA working 15:00 Afternoon Refreshments principle Some PCA examples Somatostatin homodimers/heterodimer 15:20 Sponsor Speaking section contact data CXCR4 agonist/antagonist data tareef.ahmed@atta-online.co.uk for more Thomas Koblizek Senior Scientist R&D detail Lonza 16:00 Pores for thought; analyses of 11:00 Morning refreshments TRPV1 chimeras using a bespoke heat activation assay, demonstrate that 11:20 Use of cell based GPCR assays to differences in the pore domain confer identify novel CB2 agonists and species specific pharmacological chemokine receptor antagonists sensitivity David R. Greaves Professor of Marianthi Papakosta Scientific Inflammation Biology Sir William Director at Grunenthal GmbH Dunn School of Pathology University of Oxford 16:40 Closing remarks from the Chair
  • 4. Day 2 Cell Based Assays 2012 th 27 June 2012 09:00 Registration and refreshments 12:40 Networking lunch 09:30 Opening address from the Chair 13:40 plate based screening Gene expression assay 09:40 Primary cells and 3D models in Label-free as well as assay high-throughput screening development native neuronal cell types Robin Ketteler MRC LMCB University Presentation from Pfizer College London 2:00 Sponsor Speaking section contact 10:20 Polarity markers as functional tareef.ahmed@atta-online.co.uk for more readouts of hepatic toxicity in 3D detail use of bacterial artificial chromosome to ensure physiological levels of tpj1-cherry 14:20 Beta-Arrestin 2 in Drug polarity marker expression 3 dimensional Discovery cell culture to ensure polarity and Deorphanisation functional bile canaliculi system HTS generation of transgenic animals for Biased signaling primary cell culture high throughput Scavanger imaging of live polarised hepatocytes In-vitro to in-vivo automated image analysis Xavier Leroy, Ph.D. Project Promoter Marc Bickle Head of Technology & Leader Associate Director Drug Development Studio at Max Planck Discovery Dept. Actelion Institute of Molecular Cell Biology and Pharmaceuticals Ltd Genetics 15:00 Afternoon Refreshments 11:00 Morning refreshments 15:20 Sponsor Speaking section contact tareef.ahmed@atta-online.co.uk for more 11:20 Application of in vitro 3D models detail for drug discovery More complex and therefore 16:00 High-Content screen for physiologically more relevant cell-based inhibitors of cell migration in cancer assays will ultimately be more predictive metastasis using adenoviral knock- than current 2D-based assays. down, high-throughput wound healing Technologies and assay set-up for assay which we developed to identify medium-throughput compound screening novel genes involved in metastatic cell in 3D (co-) cultures migration. Genes whose knock-down High-content analysis is a versatile inhibit cell migration were identified technology platform to capture complex by their effect on the open wound cell-based assays. Remko de Pril Galapagos Team Applications in oncology, virology and Leader Target Discovery and High- safety pharmacology Content Screening 16:40 Closing remarks from the Chair Eberhard Krausz, Director, Assay Development & Target Validation, 16:50 End of the conference Enabling Biology, Janssen Research & Development, Belgium 12:00 3D Microtissues for Early Compound De-Risking Jens Kelm, PhD, co-founder of InSphero AG
  • 5. Registration Form for Cell Based Assays 2012 26th -27th June 2012, London UK. DELEGATE DETAILS Please complete fully and clearly in capital letters and e-mail it to tareef.ahmed@atta-online.co.uk Please photocopy for additional delegates. Price: £499 Title: Forename: Surname: Job Title: Department/Division: Company/Organisation: Email: Address: Town/City: Post/Zip Code: Country: Direct Tel: Direct Fax: Mobile: Switchboard: Signature: Date: I agree to be bound by ATTA’s Terms and Conditions of Booking. Payment: If payment is not made at the time of booking, then an invoice will be issued and must be paid immediately and prior to the start of the event. If payment has not been received then credit card details will be requested and payment taken before entry to the event. Bookings within 7 days of event require payment on booking. Access to the Document Portal will not be given until payment has been received. Substitutions/Name Changes: If you are unable to attend you may nominate, in writing, another delegate to take your place at any time prior to the start of the event. Two or more delegates may not ‘share’ a place at an event. Please make separate bookings for each delegate. Cancellation: If you wish to cancel your attendance at an event and you are unable to send a substitute, then we will refund/credit 50% of the due fee less a £50 administration charge, providing that cancellation is made in writing and received at least 28 days prior to the start of the event. Regretfully cancellation after this time cannot be accepted. We will however provide the conferences documentation via the Document Portal to any delegate who has paid but is unable to attend for any reason. Due to the interactive nature of the Briefings we are not normally able to provide documentation in these circumstances. We cannot accept cancellations of orders placed for Documentation or the Document Portal as these are reproduced specifically to order. If we have to cancel the event for any reason, then we will make a full refund immediately, but disclaim any further liability. Alterations: It may become necessary for us to make alterations to the content, speakers, timing, venue or date of the event compared to the advertised programme