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asmase+/+ and asmase−/− mice, maintained in an sv129xBl/6 background, were propagated using heterozygous breeding pairs.
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Lentiviruses were propagated using standard procedures.
AdiPS cell cultures were propagated using standard protocols.
Both cell lines were propagated using ATCC protocols.
CPMV was propagated using Vigna unguiculata (black eyed peas) plants, and wild-type TMV and TMVLys mutants were propagated using Nicotiana benthamiana plants (a tobacco species).
Phage 812 was propagated using stock lysate.
All plasmids have been propagated using Escherichia coli DH5alpha.
Plasmid DNA were propagated and purified using a plasmid isolation kit (Qiagen, Valencia, CA, USA).
Human CEnCs were isolated and propagated using a dual media approach as illustrated (Fig. 1A).
Plants were propagated and transformed using previously published methods [61].
Cells were propagated and subcultured using conditions indicated by the supplier.
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