Schneider
New stable cell line derived from this cell line: A N-expressing stable S2R+ cell line was created.
New stable cell line derived from this cell line: Stable S2R+ cell lines were generated that stably express the metallothionein promoter-driven SAM (synergistic activation mediator) complex.
S2 cells were obtained from the laboratory of Norbert Perrimon.
S2R+ cells were obtained from the DRSC.
New stable cell line derived from this cell line: A stable S2 cell line deleted for the Pex1 gene was created.
New stable cell line derived from this cell line: A stable cell line overexpressing eGFP-GPAT4 was created. Seipin knock-in and knock-out cell lines were created.
New stable cell line derived from this cell line: S2R+ cells stably expressing Actin-Gal4 ( source:Prof . Satyajit Mayor lab, NCBS, Bangalore-India).
New stable cell line derived from this cell line: S2R+ cells stably expressing LiveDrop-GFP or f S2 cells stably expressing LiveDrop-RFP were used.
New stable cell line derived from this cell line: Stable S2R+ cell lines were created carrying C-terminally HA-tagged forms of either COX7B or human COX7B.
New stable cell line derived from this cell line: Stable S2R+ cell lines were generated carrying C-terminally HA-tagged forms of either COX7B or hhuman COX7B.
New stable cell line derived from this cell line: An Act-PE2 (prime editor 2) cell line was generated for use in prime editing. PE2 is expressed under the Act5C promoter.
New stable cell line derived from this cell line: S2R+ cells were stably transfected with copper-inducible Myc-tagged CkIalpha.
New stable cell line derived from this cell line: The SR9rg cell line was generated in which GFP reporter transgenes can be assembled efficiently by site-directed chromosomal integration of a test DNA fragment, allowing measurement of its CRE activity by flow cytometry.
S2R + cells were obtained from the laboratory of Sven Bogdan.
S2R+ (FEx 2.5%), S2R+ cells supplemented with adult fly extract used.
S2R+ cells were obtained from the Carthew lab.
S2R+ cells were obtained from the laboratory of N. Perrimon.
Source of S2R+ cells: DGRC.
Source of S2R+ cells: E. Chen (UT Southwestern).
New stable cell line derived from this cell line: A stable S2R+ cell line was generated lacking endogenous Stat92E by CRISPR/Cas9-mediated mutatgenesis.
New stable cell line derived from this cell line: S2R+ cells in which the fdl gene is deleted were obtained from the laboratory of D. Jarvis.
Both S2R+ and S2R+Wb (Wolbachia) cells were used.
S2R+ cells were obtained from the laboratory of N. Yanagawa.
New stable cell line derived from this cell line: Stable cell lines were generated to express constructs containing destabilizing domains (genetic tags that conditionally control the level of abundance of proteins of interest with specific stabilizing small-molecule drugs).
New stable cell line derived from this cell line: a stable S2R+ cell line expressing AkhR was generated.
New stable cell line derived from this cell line: stably transfected with transferrin receptor.
Expression of general hemocyte markers observed.
Expression profiling by genome tiling array for this cell line may be found at GEO: GSE16287 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE16287).
New stable cell line derived from this cell line: cell line expressed Atg8a.
S2R+ is an isolate of S2 cells that was found in the Miyake laboratory freezer. It was contributed to the Miyake lab by Imogene Schneider and is likely to be very similar to the original S2 line.
Hemocyte-like gene expression, phagocytic, adherent, flat cells; Fz+ and Wg-responsive.