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CITE-seq antibody staining
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Cryopreserved samples were thawed and sorted using the gating strategy in Fig. S3 A. Cells were then washed and stained in a CITE-seq antibody cocktail at a concentration of 8 µg/ml for 30 min on ice (Fig. S3 B). Cells were then washed three times before loading onto the 10x Chromium controller.
Copyright and License information: ©2021 Tull et al.
This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
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