a, b, Schematic representation and CRISPR/Cas9 genome editing strategy for the Cd40G5 (a) and Cd40lgSrtA (b) alleles. c, Restriction fragment length polymorphism (RFLP) analysis of Cd40G5/+ mice. c, PCR products generated using primers surrunding the G5 insertion site were digetsted with KpnI and analyzed by electrophoresis on an agarose gel. Data are representative of at least two experiments. d, Southern blot analysis of Cd40lgSrtA/+ mouse. Genomic DNA was extracted, digested with XbaI, and transferred onto a nitrocellulose membrane after electrophoresis on an agarose gel. Genomic DNA fragments were detected using a probe annealing between exons 4 and 5.