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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
Comments |
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|---|---|---|---|---|---|---|---|---|---|---|
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pCBLsgRNA7 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199733 | OsU6.2-sgRNA7 scaffold | Synthetic | Tetracycline | PMID:37070560 | Vector Backbone:pYPQ131D; Vector Types:Plant Expression; Bacterial Resistance:Tetracycline | 2026-09-01 09:36:01 | 1 | ||
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pCBLsgRNA8 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199734 | TaU6-sgRNA8 scaffold | Synthetic | Tetracycline | PMID:37070560 | Vector Backbone:pYPQ131D; Vector Types:Plant Expression; Bacterial Resistance:Tetracycline | 2026-09-01 09:36:01 | 1 | ||
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pCBLsgRNA5 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199731 | ZmU6C3-sgRNA5 scaffold | Synthetic | Tetracycline | PMID:37070560 | Vector Backbone:pYPQ131D; Vector Types:Plant Expression; Bacterial Resistance:Tetracycline | 2026-09-01 09:36:01 | 1 | ||
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pCBLsgRNA4 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199730 | ZmU6C1-sgRNA4 scaffold | Synthetic | Tetracycline | PMID:37070560 | Vector Backbone:pYPQ131D; Vector Types:Plant Expression; Bacterial Resistance:Tetracycline | 2026-09-01 09:36:01 | 1 | ||
|
AD59_pEP.DonorCLYBL.TS Resource Report Resource Website |
RRID:Addgene_199227 | Expression unit for PuroR.T2A.EGFP selectable and reporter markers | Synthetic | Ampicillin | PMID:36928106 | This target site-containing donor plasmid can be used to insert a transgene(s) at the human CLYBL safe harbor locus when delivered together with Sp-gRNA expression plasmid AY27_pU6.gRNA.CLYBL (Addgene plasmid #199238) or Sa-gRNA expression plasmid AM77_pU6.Sa-gRNA.CLYBL (Addgene plasmid #199237). Combining this donor with a S. pyogenes Cas9 or a S. aureus Cas9 nuclease allows for HMEJ-mediated gene targeting. Note: to reduce the chances for off-targeting donor DNA insertions when applying the Sp-gRNA for HMEJ-based genome editing it is preferable using AW01_pU.CAG.eSpCas9(1.1).rBGpA (Addgene plasmid #199255) or a similar construct, i.e., expressing a high specificity nuclease. Combining this donor with a S. pyogenes Cas9 nickase (e.g., Addgene plasmids #199256, #199253, #199254 or #199252) or a S. aureus Cas9 nickase (Addgene plasmid #199251) leads to seamless ITPN-mediated gene targeting. | Backbone Size:2850; Vector Backbone:pBR322; Vector Types:Mammalian Expression, Gene targeting donor plasmid; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:53 | 0 | |
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BB44_pmc.DonorR5.TS Resource Report Resource Website |
RRID:Addgene_199223 | Expression unit for mCherry - monomeric derivative of DsRed fluorescent protein (Shaner et al., 2004) | Synthetic | Ampicillin | PMID:36928106 | This target site-containing donor plasmid can be used to insert a transgene at the human CCR5 safe harbor locus when delivered together with gRNA expression plasmid AY22_pgRNA.R5.1 (Addgene plasmid #100294) and a SpCas9 nuclease (HMEJ-based gene targeting) or a SpCas9.D10A nickase (ITPN-based gene targeting). Note: to reduce the chances for off-targeting donor DNA insertions when applying HMEJ-based genome editing it is preferable using AW01_pU.CAG.eSpCas9(1.1).rBGpA (Addgene plasmid #199255) or a similar construct, i.e., expressing a high specificity nuclease. Combining this donor with a S. pyogenes Cas9 nickase (e.g., Addgene plasmids #199256, #199253, #199254 or #199252) leads to seamless ITPN-mediated gene targeting. | Backbone Size:2700; Vector Backbone:pBR322; Vector Types:Mammalian Expression, Gene targeting donor plasmid; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:53 | 0 | |
|
pCBLsgRNA2 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199728 | OsU3-sgRNA2 scaffold | Synthetic | Tetracycline | PMID:37070560 | Vector Backbone:pYPQ132D; Vector Types:Plant Expression; Bacterial Resistance:Tetracycline | 2026-09-01 09:36:01 | 1 | ||
|
pCBLsgRNA3 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199729 | TaU3-sgRNA3 scaffold | Synthetic | Tetracycline | PMID:37070560 | Vector Backbone:pYPQ131D; Vector Types:Plant Expression; Bacterial Resistance:Tetracycline | 2026-09-01 09:36:01 | 1 | ||
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pCBLgRNA Resource Report Resource Website 1+ mentions |
RRID:Addgene_199726 | sgRNA scaffold | Synthetic | Spectinomycin | PMID:37070560 | Vector Backbone:pYPQ141D; Vector Types:Plant Expression; Bacterial Resistance:Spectinomycin | 2026-09-01 09:36:01 | 1 | ||
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pCBL101.1 Resource Report Resource Website |
RRID:Addgene_199724 | Multiple Cloning Site, NPTII | Synthetic | Spectinomycin | PMID:37070560 | Vector Backbone:pCBL101; Vector Types:Plant Expression; Bacterial Resistance:Spectinomycin | "GAGACC" to "GATACC" | 2026-09-01 09:36:01 | 0 | |
|
pCBL101 Resource Report Resource Website 1+ mentions |
RRID:Addgene_199722 | NPTII | Synthetic | Spectinomycin | PMID:37070560 | Vector Backbone:pTF101.1; Vector Types:Plant Expression; Bacterial Resistance:Spectinomycin | 2026-09-01 09:36:01 | 1 | ||
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pCBL101-RUBY Resource Report Resource Website |
RRID:Addgene_199723 | 35S-RUBY | Synthetic | Spectinomycin | PMID:37070560 | Addgene sequencing identified partial duplication of the CaMV 35S enhancer element. Depositing lab has confirmed that the duplication was present in their original stock of the plasmid and does not disrupt RUBY function. | Vector Backbone:pCBL101; Vector Types:Plant Expression; Bacterial Resistance:Spectinomycin | 2026-09-01 09:36:01 | 0 | |
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pcDNA3.1_27F3_hFc Resource Report Resource Website |
RRID:Addgene_199619 | DARPin-hFc 27F3 | Synthetic | Ampicillin | PMID:36314779 | HTC DARPin name 008-855-2309-D7 | Backbone Marker:Invitrogen; Backbone Size:6800; Vector Backbone:pcDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:59 | 0 | |
|
pQIq_MRGS_HIS8_(27G2)_FLAG Resource Report Resource Website 1+ mentions |
RRID:Addgene_199616 | DARPin-FLAG 27G2 | Synthetic | Ampicillin | PMID:36314779 | HTC DARPin name 008-855-2308-A9 | Backbone Marker:Qiagen; Backbone Size:4037; Vector Backbone:pQE30; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:59 | 1 | |
|
pcDNA3.1_ E3_5 _hFc Resource Report Resource Website |
RRID:Addgene_199617 | DARPin-hFc E3_5 (control) | Synthetic | Ampicillin | PMID:36314779 | HTC DARPin name 008-782-2400-H3 | Backbone Marker:Invitrogen; Backbone Size:6800; Vector Backbone:pcDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:59 | 0 | |
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pQIq_MRGS_HIS8_( E3_5)_FLAG Resource Report Resource Website |
RRID:Addgene_199612 | DARPin-FLAG E3_5 (control) | Synthetic | Ampicillin | PMID:36314779 | HTC DARPin name 008-782-2400-H3 | Backbone Marker:Qiagen; Backbone Size:4037; Vector Backbone:pQE30; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:59 | 0 | |
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pLenti-PE2max-BSD Resource Report Resource Website 1+ mentions |
RRID:Addgene_191102 | PEmax-P2A-BSD | Synthetic | Ampicillin | PMID:37119812 | Backbone Marker:Hyongbum Kim; Backbone Size:8228; Vector Backbone:pLenti-PE2-BSD; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin | Changed R221K, N394K, H840A from SpCas9 | 2026-09-01 09:33:37 | 1 | |
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pLenti-NRCH-PE2-BSD Resource Report Resource Website |
RRID:Addgene_191101 | NRCH-PE2-BSD | Synthetic | Ampicillin | PMID:37119812 | Backbone Marker:Hyongbum Kim; Backbone Size:8228; Vector Backbone:pLenti-PE2-BSD; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin | 2026-09-01 09:33:37 | 0 | ||
|
AZ64_pE.DonorCLYBL.TS Resource Report Resource Website |
RRID:Addgene_199228 | Expression unit for EGFP reporter | Synthetic | Ampicillin | PMID:36928106 | This target site-containing donor plasmid can be used to insert a transgene(s) at the human CLYBL safe harbor locus when delivered together with Sp-gRNA expression plasmid AY27_pU6.gRNA.CLYBL (Addgene plasmid #199238) or Sa-gRNA expression plasmid AM77_pU6.Sa-gRNA.CLYBL (Addgene plasmid #199237). Combining this donor with a S. pyogenes Cas9 or a S. aureus Cas9 nuclease allows for HMEJ-mediated gene targeting. Note: to reduce the chances for off-targeting donor DNA insertions when applying the Sp-gRNA for HMEJ-based genome editing it is preferable using AW01_pU.CAG.eSpCas9(1.1).rBGpA (Addgene plasmid #199255) or a similar construct, i.e., expressing a high specificity nuclease. Combining this donor with a S. pyogenes Cas9 nickase (e.g., Addgene plasmids #199256, #199253, #199254 or #199252) or a S. aureus Cas9 nickase (Addgene plasmid #199251) leads to seamless ITPN-mediated gene targeting. | Backbone Size:2850; Vector Backbone:pBR322; Vector Types:Mammalian Expression, Gene targeting donor plasmid; Bacterial Resistance:Ampicillin | 2026-09-01 09:35:53 | 0 | |
|
pAAV_CMV::hTfR-GFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_199714 | hTfR-GFP | Synthetic | Ampicillin | PMID:37098770 | Please visit https://doi.org/10.1101/2023.03.03.531050 for bioRxiv preprint. In the original study XL1 Blue E. coli are used for amplifying plasmids. | Vector Backbone:pAAV; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin | 2026-09-01 09:36:01 | 1 |
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