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Decoding the Spatial code using Proteomic Spatial Phenotyping

Webinar

Wednesday, 9th October, 2024  
15:00 to 16:00 CEST (Berlin, Paris, Madrid)

Register

Embark on a journey of discovery in spatial biology with this webinar. We will lead you through a streamlined workflow, showing the transition from sample preparation to multiplexing to minimizing workflow bottlenecks and maximizing experimental throughput. Mateo TL and Mica offer an innovative solution by providing advanced sample preparation to ensure most optimal sample integrity. Moreover, to drive down disease progression and increase response to therapy, there is a strong need to deliver context to better understand the real complexity of biological interactions. Hence, by harnessing the power of Cell DIVE, researchers can unravel the spatial heterogeneity of cellular populations, uncovering hidden insights that traditional imaging techniques fail to capture. Along this way, explore the transformative power of Aivia software for precise spatial phenotyping and data analysis. Don't miss this exclusive opportunity to revolutionize your research approach. Secure your spot now!

For more information, please contact us at webinar@avantorsciences.com

Presented by:

  Michael Smith, Ph.D. is Application Manager at Leica Microsystems. He completed a Ph.D. in the genetics of DNA repair at Columbia University and a postdoctoral fellowship in genome integrity and cellular aging at Memorial Sloan Kettering Cancer Center, where he leveraged microscopy to understand the real-time dynamics of DNA homeostasis. His passion for answering biological questions using imaging technologies led him to his current position, where he provides technical expertise and customer support for a range of Leica products, focusing on spatial biology solutions.
 
  Daniel Smeets is an Advanced Workflow Specialist at Leica Microsystems. He obtained his PhD in biology (Cell Biology and Epigenetics) from the University of Munich (LMU) in 2013 and during his PhD studies also spent over a year at the University of Oxford/UK. During his PhD studies he was interested in the higher-order structure of chromatin in the interphase nucleus of mammals and how this interplays with essential nuclear functions like transcription and replication. He used mammalian female X Chromosome inactivation as a model system which he studied with methods like super-resolution microscopy, confocal microscopy and FRAP, as well as immunochemistry, DNA- and RNA-FISH.