We narrowed to 1,402 results for: V2
-
Plasmid#237972PurposeEncodes TRAV14/DV4 allele, P2A, and TRBC to generate TCRs via cloningDepositorAvailable sinceJune 12, 2025AvailabilityAcademic Institutions and Nonprofits only
-
TRAV30
Plasmid#237987PurposeEncodes TRAV30 allele, P2A, and TRBC to generate TCRs via cloningDepositorAvailable sinceJune 12, 2025AvailabilityAcademic Institutions and Nonprofits only -
TRAV19
Plasmid#237976PurposeEncodes TRAV19 allele, P2A, and TRBC to generate TCRs via cloningDepositorAvailable sinceJune 12, 2025AvailabilityAcademic Institutions and Nonprofits only -
TRAV12-2
Plasmid#237968PurposeEncodes TRAV12-2 allele, P2A, and TRBC to generate TCRs via cloningDepositorAvailable sinceJune 12, 2025AvailabilityAcademic Institutions and Nonprofits only -
lenti-gRNA
Plasmid#226867PurposeLentiviral expression of Sp-gRNA with BlpI and BstXI restriction sites for gRNA spacer cloning. Also expresses BFP.DepositorInsertLenti Sp-gRNA
UseLentiviralPromotermU6Available sinceFeb. 10, 2025AvailabilityAcademic Institutions and Nonprofits only -
-
Lentiviral click editor (CE1) plasmid - LTR-pEF1a-PCV2-nCas9-EcKlenow (DRR921)
Plasmid#217798PurposeLentiviral plasmid to produce the prototypical CE1 construct (PCV2-nCas9-EcKlenow), expressed from the EF1a promoterDepositorInsertXTEN-nSpCas9-BPNLS-EcKlenow(-exo)-BPNLS
UseCRISPR and LentiviralTagsBPNLSExpressionMammalianMutationnSpCas9(H840A); EcKlenow(-exo;D355A/E357A)PromoterEF1aAvailable sinceSept. 6, 2024AvailabilityAcademic Institutions and Nonprofits only -
pSpCas9-2A-Puro-RAB7A-gRNA2 (PX459)
Plasmid#221552PurposeExpresses Cas9 and gRNA for disruption of Rab7A gene in human cellsDepositorAvailable sinceJuly 15, 2024AvailabilityAcademic Institutions and Nonprofits only -
pSpCas9(BB)-2A-Puro-SMCR8
Plasmid#83440PurposeExpresses Cas9 and a gRNA targeting SMCR8DepositorAvailable sinceJuly 15, 2024AvailabilityAcademic Institutions and Nonprofits only -
pGB
Plasmid#204744PurposegRNA-Bsd expression vectorDepositorTypeEmpty backboneExpressionMammalianAvailable sinceJune 13, 2024AvailabilityAcademic Institutions and Nonprofits only -
-
B2M-SDMutation-gRNA
Plasmid#215547PurposegRNA targeting B2M to introduce splice donor mutation on the first intron of the locusDepositorInsertB2M (B2M Human)
UseCRISPRAvailable sinceMarch 14, 2024AvailabilityAcademic Institutions and Nonprofits only -
pLentiCriprV2-sgRNA-PER1-#1
Plasmid#189987PurposeLentiviral Cas9/sgRNA vector targeting C-terminus of hPER1, works with Addgene 189979-189982DepositorInsertPeriod1 (PER1 Human)
UseCRISPR and LentiviralAvailable sinceFeb. 9, 2024AvailabilityAcademic Institutions and Nonprofits only -
LentiCRISPRCreb5gRNA
Plasmid#195021PurposeSequence specific sgRNA that guide Cas9 to the genomic region encoding the bovine Creb5 DNA binding domainDepositorAvailable sinceFeb. 8, 2024AvailabilityAcademic Institutions and Nonprofits only -
Lenti-sgRNA-Cre-GpNLuc-sgmZBP1#1
Plasmid#208387PurposeLentiviral vector expressing Cas9, GpNLuc, and sgRNA targeting murine ZBP1#1 gene.DepositorAvailable sinceJan. 11, 2024AvailabilityAcademic Institutions and Nonprofits only -
Lenti-sgRNA-Cre-GpNLuc-sgmZBP1#2
Plasmid#208388PurposeLentiviral vector expressing Cas9, GpNLuc, and sgRNA targeting murine ZBP1#2 gene.DepositorAvailable sinceJan. 11, 2024AvailabilityAcademic Institutions and Nonprofits only -
LentiCRISPRv2-sgCD20
Plasmid#209749PurposeLentiviral transfer plasmid to express Cas9 and a gRNA targeting the human CD20 gene, MS4A1.DepositorInsertMS4A1 (MS4A1 Human)
UseLentiviralAvailable sinceNov. 30, 2023AvailabilityAcademic Institutions and Nonprofits only -
MsCLYBL_sgRNA6
Plasmid#111295PurposeCRISPR KO murine CLYBLDepositorInsertsgRNA6 against murine CLYBL
UseCRISPR and LentiviralExpressionMammalianAvailable sinceNov. 16, 2023AvailabilityAcademic Institutions and Nonprofits only -
LENTICRISPR-TKT_sgRNA2
Plasmid#201625PurposeCRISPR/Cas9-mediated gene knock-outDepositorInsertTKT (TKT Human)
UseCRISPR and LentiviralAvailable sinceJuly 26, 2023AvailabilityAcademic Institutions and Nonprofits only -
LENTICRISPR-TKT_sgRNA1
Plasmid#201624PurposeCRISPR/Cas9-mediated gene knock-outDepositorInsertTKT (TKT Human)
UseCRISPR and LentiviralAvailable sinceJuly 26, 2023AvailabilityAcademic Institutions and Nonprofits only