Making Multiplexed Imaging Flexible - Combining Essential Markers with Established Antibody Panels

多路复用 抗体 计算机科学 计算生物学 生物 免疫学 电信
作者
Ashik Jawahar Deen,Pranauti Panshikar,Tony Ullman,Eleanor M O`Roberts,David H. Krantz,Carolina Oses,Charlotte Stadler
标识
DOI:10.2139/ssrn.4653168
摘要

Hyperplexed immunofluorescence (IF) can be achieved using different commercially available platforms, often making use of conjugated antibodies detected in iterative cycles. A growing portfolio of pre-conjugated antibodies are offered by the providers, as well as the possibility for in house conjugation. For many conjugation methods and kits, there are limitations in which antibodies can be used, and conjugation results are sometimes irreproducible. The conjugation process can limit or slow down the progress of studies requiring conjugation of essential markers needed for a given project. Here, we demonstrate a protocol combining manual indirect immunofluorescence (IF) of primary antibodies, followed by antibody elution and staining with multiplexed panels of commercially pre-conjugated antibodies. We present detailed protocols for applying the workflow on fresh frozen and formalin fixed paraffin embedded tissue sections as well as tissue microarrays. The protocol is demonstrated for integration upstream of the Phenocycler technology, however it could be combined with other downstream multiplexing platforms.

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