Invitrogen
New stable cell line derived from this cell line: A CRISPR method for S2 cells that can be adapted for both knock-in and knock-out of any gene was developed. The followind lines were created (author designations): S2-Cas9Par, S2-Plk4 CRISPR null line 1, S2-Plk4 CRISPR null line 2.2, S2-Plk4 CRISPR null line 7, S2-Ana2 CRISPR null line 2, S2-Ana2 CRISPR null line 4, S2-Ana2 CRISPR null line 5, S2-ana2 CRISPR null line 12, Ana2 CRISPR null line 15, and Ana2 CRISPR null line 17. Note that Plk4 is SAK in FlyBase and Ana2 is ana2 in FlyBase.
New stable cell line derived from this cell line: The following stable S2 cell lines were created: S2-OsTir1-CG11247/Saft-AID, S2-OsTir1-Su(Hw)-AID, S2-OsTir1-Phaser-AID, S2-OsTir1-G9a-AID, S2-OsTir1-Lft-deltaDLM3, S2-TurboID-GFP, S2-CG11247/Saft-TurboID.
New stable cell line derived from this cell line: The following derivative cell lines were generated: Parental OsTir-expressing S2 cell line, Trf2 C-terminally-tagged AID S2 cell line, Tbp-N-terminally-tagged AID S2 cell line, Dref-N-terminally-tagged AID S2 cell line, TfIIA-L-C-terminally-tagged AID S2 cell line, Chro-N-terminally-tagged AID S2 cell line.
New stable cell line derived from this cell line: Stable S2 cell lines were created to study chromatin remodeling. The base S2[OsTir1] was created and selected core proteins from the four main sub-families of ATP-dependent chromatin remodelers (Snr1, Iswi, Ino80, and Chd1) as well as SWI/SNF component Brd7-9 were inserted to create S2OsTir1-Snr1-AID, S2OsTir1-Iswi-AID, S2OsTir1-Ino80-AID, S2OsTir1-Chd1-AID, and S2OsTir1-Brd7-AID for component depletion studies.
New stable cell line derived from this cell line: Centriolar proteins were tagged with GFP at either the N- or C- terminus and used to create stable S2 cell lines. S2 cell lines constitutively expressing the following constructs were created: asl-GFP, Sas-6-GFP, ana1-GFP, GFP-ana1, Cep135-GFP, ana3-GFP, Rcd4-GFP, ana2-GFP, GFP-asl.
New stable cell line derived from this cell line: A stable S2- mCherry:Tubulin-GFP:cid cell line was created. This was accomplished by transfecting cells stably expressing GFP:CID (from Gary Karpen) with inducible mCherry-alpha-tubulin.
New stable cell line derived from this cell line: A stable S2 cell line expressing GFP-Lam and mCherry-alpha-tubulin was created. Stable S2 lines expressing RFP(Unk)-Lam wild type and constructs in which the CDK sites were mutated were generated. A stable S2 cell line that expressed GFP-baf and mCherry-alpha-tubulin was created.
New stable cell line derived from this cell line: Stable cell lines were constructed for expression of brm constructs (recBRM-V5 and recBRM-K804R-V5).
S2 cells obtained from Invitrogen. Many features of the S2 cell line suggest that it is derived from a macrophage-like lineage.
New stable cell line derived from this cell line: S2 cell lines stably expressing Rren\LUC were created.
New stable cell line derived from this cell line: Stable S2 cell lines expressing Tag:polyHis-tagged-PGRP-LF were generated.
New stable cell line derived from this cell line: Stable S2 cell lines overexpressing an N-terminal fragment of hh were generated.
New stable cell line derived from this cell line: Stable S2 cell lines expressing Human ADAM33 under the control of the Act5C or metallothionein promoter were generated.