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Cellosaurus HEK293 SCN1A/SCN1B/SCN2B (CVCL_WS18)

[Text version]
Cell line name HEK293 SCN1A/SCN1B/SCN2B
Accession CVCL_WS18
Resource Identification Initiative To cite this cell line use: HEK293 SCN1A/SCN1B/SCN2B (RRID:CVCL_WS18)
Comments Characteristics: Co-transfected the constructs pT-SCN1A:3X-FLAG and pT-SCN1B:cMyc-IRES-SCN2B:HA.
Transfected with: HGNC; 10585; SCN1A.
Transfected with: HGNC; 10586; SCN1B.
Transfected with: HGNC; 10589; SCN2B.
Transformant: NCBI_TaxID; 28285; Adenovirus 5.
Derived from site: In situ; Fetal kidney; UBERON=UBERON_0002113.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0045 (HEK293)
Sex of cell Female
Age at sampling Fetus
Category Transformed cell line
Publications

PubMed=23086956; DOI=10.1074/jbc.M112.421883
Thompson C.H., Porter J.C., Kahlig K.M., Daniels M.A., George A.L. Jr.
Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expression.
J. Biol. Chem. 287:42001-42008(2012)

Cross-references
Encyclopedic resources Wikidata; Q94094939
Entry history
Entry creation05-Jul-2019
Last entry update29-Jun-2023
Version number5