ID   HEK293 SCN1A/SCN1B/SCN2B
AC   CVCL_WS18
DR   Wikidata; Q94094939
RX   PubMed=23086956;
CC   Characteristics: Co-transfected the constructs pT-SCN1A:3X-FLAG and pT-SCN1B:cMyc-IRES-SCN2B:HA.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:10585; SCN1A.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:10586; SCN1B.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:10589; SCN2B.
CC   Transformant: NCBI_TaxID; 28285; Adenovirus 5.
CC   Derived from site: In situ; Fetal kidney; UBERON=UBERON_0002113.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0045 ! HEK293
SX   Female
AG   Fetus
CA   Transformed cell line
DT   Created: 05-07-19; Last updated: 19-12-24; Version: 7
//
RX   PubMed=23086956; DOI=10.1074/jbc.M112.421883; PMCID=PMC3516746;
RA   Thompson C.H., Porter J.C., Kahlig K.M., Daniels M.A.,
RA   George A.L. Jr.;
RT   "Nontruncating SCN1A mutations associated with severe myoclonic
RT   epilepsy of infancy impair cell surface expression.";
RL   J. Biol. Chem. 287:42001-42008(2012).
//