2020 May 26 - Visualize Splice Variants, Short Targets, and Point Mutations at Single Cell Resolution
Anushka Dikshit, Ph.D.
Applications Scientist, Advanced Cell Diagnostics
Watch Video:
Helly Pimentel, MBA
Product Manager, Advanced Cell Diagnostics
Outline:
Envision the detection of splice variants, short/highly homologous genes, and point mutations at single cell resolution. The BaseScope™ Assays enable highly specific and sensitive detection and visualization of RNA targets down to one nucleotide difference, in situ, with spatial mapping and morphological context.
This webinar will highlight the top applications that are supported by the BaseScope Assays.
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 Assays
- Introduction to the BaseScope technology and workflow
- Applications that necessitate the use of the BaseScope Assays
- Address frequently asked questions regarding the BaseScope Assays
