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. Author manuscript; available in PMC: 2020 Mar 23.
Published in final edited form as: Nature. 2019 Sep 23;575(7782):371–374. doi: 10.1038/s41586-019-1611-7

Extended Data Fig. 10. Generation of Unc93b1S282A knock-in mice and B-cell stimulation with LPS.

Extended Data Fig. 10.

(a) CRISPR/Cas-9 strategy to generate Unc93b1S282A knock-in mice. Blue line indicates the guide sequence. Red bases indicated the edited codon. A representative sequencing trace of genomic DNA from an edited founder mouse is shown. (b) B cell proliferation in CSFE-labeled splenocyte cultures of the indicated mouse genotypes after stimulation for 3 days with increasing doses of LPS. The proliferation index is defined as geometric fluorescent intensity (gMFI) CSFEUnstim: gMFI CFSESample. Each curve shows the dose response of cells from three mice. Data are mean ± s.d. p values determined by two-way ANOVA followed by a Sidak’s posttest, ns = not significant. (c) Gating strategy for B cell stimulation assay.