This cell line, modified from hESC line WIBR3, contains a heterozygous form of the G2019S mutation in LRRK2 found in approximately 5% of autosomal dominant inherited PD cases.

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Lot Number Culture Platform Lot Description Banked By Passage Number Protocol Product Information & Testing
WB69004 iSCORE 01 medium / 2x CF1 MEF WiCell 33 WiCell Feeder Based (MEF) Protocol 01 for Culture of MJFF iSCORE Lines PDF

WiCell