We narrowed to 34,114 results for: IND;
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Plasmid#67537PurposeEasyClone system-based yeast integrative vector carrying loxP-flanked CaLYS5 marker, integration into S. cerevisiae XI-5 chromosomal location, USER site for cloning, amp resistanceDepositorTypeEmpty backboneUseCre/Lox; IntegrativeExpressionYeastAvailable SinceNov. 3, 2015AvailabilityAcademic Institutions and Nonprofits only
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Human messenger-RBP sgRNA library
Pooled Library#168791PurposeKnockout library targeting human mRNA binding proteins with 10 sgRNAs/gene.DepositorExpressionMammalianSpeciesHomo sapiensUseCRISPR and LentiviralAvailable SinceJuly 30, 2021AvailabilityAcademic Institutions and Nonprofits only -
pSMAL-CellTag-multi-v1 barcode library
Pooled Library#206045PurposeThe CellTag multi library of barcodes can be used to clonally label cells with DNA barcodes. These barcodes can be profiled directly with single-cell RNA and ATAC sequencing, to allow clonal trackingDepositorUseLentiviralAvailable SinceNov. 2, 2023AvailabilityAcademic Institutions and Nonprofits only -
Mouse messenger-RBP sgRNA library
Pooled Library#169082PurposeRetroviral knockout library targeting mouse mRNA binding proteins with 10 sgRNAs/gene.DepositorExpressionMammalianSpeciesMus musculusUseCRISPR and LentiviralAvailable SinceSept. 10, 2021AvailabilityAcademic Institutions and Nonprofits only -
pgRNAtet-lvaA
Plasmid#106397PurposeGuide RNA plasmid targeting lvaA on BBR1-UP originDepositorInsertsgRNA towards lvaA in Pseudomonas putida
UseCRISPR and Synthetic BiologyExpressionBacterialAvailable SinceMarch 22, 2018AvailabilityAcademic Institutions and Nonprofits only -
pTA-HUH
Plasmid#221152PurposeHisG-URA3-HisG recycling type marker in pTAs for Yarrowia lipolyticaDepositorInsertHisG-URA3-HisG
ExpressionBacterial and YeastAvailable SinceJuly 2, 2024AvailabilityAcademic Institutions and Nonprofits only -
pCAS1yl
Plasmid#73226PurposeConstitutive expression of Cas9 and sgRNA in Yarrowia lipolytica cellsDepositorInsertsCas9
sgRNA
UseCRISPR; In y. lipolyticaExpressionBacterialPromoterunknownAvailable SinceJune 16, 2016AvailabilityAcademic Institutions and Nonprofits only -
pCMU-4
Plasmid#172353PurposeCRISPR gene editing in Streptomyces, codon-optimized Cas9 behind theophylline riboswitch and D4 promoter, with custom gRNADepositorInsertD4-TheoR-cas9
UseCRISPR and Synthetic BiologyExpressionBacterialPromoterD4Available SinceDec. 10, 2021AvailabilityAcademic Institutions and Nonprofits only -
Glycogene CRISPR Library
Pooled Library#140961PurposeKnockout library targeting human genes involved in cellular glycosylation.DepositorSpeciesHomo sapiensUseCRISPR and LentiviralAvailable SinceSept. 9, 2020AvailabilityAcademic Institutions and Nonprofits only -
SPECS library
Pooled Library#127842PurposeFor performing high-throughput cell state-specific synthetic promoter screeningDepositorSpeciesSyntheticUseLentiviralAvailable SinceAug. 22, 2020AvailabilityAcademic Institutions and Nonprofits only -
Human Kinase Domain-Focused CRISPR Knockout Library
Pooled Library#117725PurposeDesigned for genomic deletion screening of protein kinases by targeting the kinase domains.DepositorExpressionMammalianSpeciesHomo sapiensUseCRISPR and LentiviralAvailable SinceJan. 4, 2019AvailabilityAcademic Institutions and Nonprofits only -
Human lentiviral CRISPR library_v1
Pooled Library#69763PurposeUsed for genome scale lentiviral CRISPR screening. Target sites were chosen in a region close to the translation initiation site.DepositorExpressionMammalianSpeciesHomo sapiensUseCRISPR and LentiviralAvailable SinceFeb. 9, 2016AvailabilityAcademic Institutions and Nonprofits only -
Human Paralog Knockout Library (pgPEN)
Pooled Library#171172PurposeInduces knockouts of paralogous gene pairs. Plasmids express a pair of guide RNAs targeting either individual genes or a pair of paralogs.DepositorExpressionMammalianSpeciesHomo sapiens and SyntheticUseCRISPR and LentiviralAvailable SinceSept. 28, 2021AvailabilityAcademic Institutions and Nonprofits only -
Human SLC KO Library
Pooled Library#132552PurposeKnockout library targeting human SLC proteins.DepositorExpressionMammalianSpeciesHomo sapiensUseCRISPR and LentiviralAvailable SinceMay 7, 2020AvailabilityAcademic Institutions and Nonprofits only -
pAH33
Plasmid#226850PurposeTo constitutively overexpress Opa1 from the safe harbor locus Rosa26 in MEFDepositorAvailable SinceFeb. 11, 2025AvailabilityAcademic Institutions and Nonprofits only -
pUC19-U6-SpCas9_gRNA-OPA1-del_exon5-gRNA1a_(CJT90)
Plasmid#226989PurposepUC19 plasmid with U6 promoter and SpCas9 gRNA to create an OPA1-del_exon5 cell line via nuclease mediate excision, gRNA 1a must be used with gRNA 2a or 2bDepositorInsertSpCas9 gRNA 1a to create OPA1-del_exon5
UseCRISPRExpressionMammalianPromoterU6Available SinceNov. 21, 2024AvailabilityAcademic Institutions and Nonprofits only -
pUC19-U6-SpCas9_gRNA-OPA1-del_exon5-gRNA2a_(CJT91)
Plasmid#226991PurposepUC19 plasmid with U6 promoter and SpCas9 gRNA to create an OPA1-del_exon5 cell line via nuclease mediate excision, gRNA 2a must be used with gRNA 1a or 1bDepositorInsertSpCas9 gRNA 2a to create OPA1-del_exon5
UseCRISPRExpressionMammalianPromoterU6Available SinceNov. 21, 2024AvailabilityAcademic Institutions and Nonprofits only -
pUC19-U6-SpCas9_gRNA-OPA1-createR194G-A6-gRNA_(CJT88)
Plasmid#226987PurposepUC19 plasmid with U6 promoter and SpCas9 gRNA to create an OPA1-R194G cell line via adenine base editing (target base in position A6)DepositorInsertSpCas9 gRNA A6 to create OPA1-R194G
UseCRISPRExpressionMammalianPromoterU6Available SinceNov. 6, 2024AvailabilityAcademic Institutions and Nonprofits only -
pUC19-U6-SpCas9_gRNA-OPA1-createR194G-A7-gRNA_(CJT89)
Plasmid#226986PurposepUC19 plasmid with U6 promoter and SpCas9 gRNA to create an OPA1-R194G cell line via adenine base editing (target base in position A7)DepositorInsertSpCas9 gRNA A7 to create OPA1-R194G
UseCRISPRExpressionMammalianPromoterU6Available SinceNov. 6, 2024AvailabilityAcademic Institutions and Nonprofits only -
pUC19-U6-SpCas9_gRNA-OPA1-del_exon5-gRNA2b_(CJT93)
Plasmid#226992PurposepUC19 plasmid with U6 promoter and SpCas9 gRNA to create an OPA1-del_exon5 cell line via nuclease mediate excision, gRNA 2b must be used with gRNA 1a or 1bDepositorInsertSpCas9 gRNA 2b to create OPA1-del_exon5
UseCRISPRExpressionMammalianPromoterU6Available SinceNov. 5, 2024AvailabilityAcademic Institutions and Nonprofits only