2019 Sept 25 - Visualize Splice Variants, Short Targets, and Point Mutations at Single Cell Resolution
Helly Liu Pimentel, MBA
Associate Product Manager
Watch Video:
Anushka Dikshit, PhD.
Applications Scientist

Envision the detection of splice variants, short/highly homologous genes, and point mutations at single cell resolution. The BaseScope™ technology enables highly specific and sensitive detection and visualization of RNA targets down to one nucleotide difference, in situ, with spatial mapping and morphological context. 

Who should attend:
  • Researchers interested in visualizing splice variants/exon junctions
  • Researchers interested in visualizing short and highly homologous sequences such as CRISPR constructs and T-cell receptors (TCRs)
  • Researchers interested in simultaneously visualizing wild types and point mutations
  • Researchers working with FFPE cells & tissues (TMAs) and fresh or fixed frozen tissues
  • Researchers interested in dual BaseScope ISH and IHC/IF assays in the same tissue section
Learning Objectives:
  • Significance of spatial profiling using the BaseScope Assay
  • Introduction to the BaseScope technology and workflow
  • Applications that necessitate the use of the BaseScope Assay
  • Address frequently asked questions regarding the BaseScope Assay
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