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
Outline:
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
