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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
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INCTbiosyn-pAct-AtINT5 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127531 | Integrase 5 coding sequence codon optimized for A. thaliana expression. | Other | Kanamycin | PMID:32444777 | The whole insert (promoter, CDS and terminator) was synthesized and cloned into backbone plasmid. The Actin 2 promoter came from Aragao, F. J. L., et al. Plant Science 168, 1227-1233 (2005) and the NOS terminator sequence from pBI426 plasmid of Datla, R.S., et al. Gene 101, 239-246 (1991). The original integrase 5 coding sequence (before A. thaliana codon optimization) was obtained from Yang, L. et al. Nat. Methods 11, 1261-1266 (2014). | Vector Backbone:pUC57; Vector Types:Plant Expression; Bacterial Resistance:Kanamycin | 2026-08-15 01:04:37 | 1 | |
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INCTbiosyn-pAct-AtINT4 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127530 | Integrase 4 coding sequence codon optimized for A. thaliana expression. | Other | Kanamycin | PMID:32444777 | The whole insert (promoter, CDS and terminator) was synthesized and cloned into backbone plasmid. The Actin 2 promoter came from Aragao, F. J. L., et al. Plant Science 168, 1227-1233 (2005) and the NOS terminator sequence from pBI426 plasmid of Datla, R.S., et al. Gene 101, 239-246 (1991). The original integrase 4 coding sequence (before A. thaliana codon optimization) was obtained from Yang, L. et al. Nat. Methods 11, 1261-1266 (2014). | Vector Backbone:pUC57; Vector Types:Plant Expression; Bacterial Resistance:Kanamycin | 2026-08-15 01:04:37 | 1 | |
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INCTbiosyn-pAct-AtINTBxb1 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127536 | Integrase Bxb1 coding sequence codon optimized for A. thaliana expression. | Other | Ampicillin | PMID:32444777 | The whole insert (promoter, CDS and terminator) was synthesized and cloned into backbone plasmid. The Actin 2 promoter came from Aragao, F. J. L., et al. Plant Science 168, 1227-1233 (2005) and the NOS terminator sequence from pBI426 plasmid of Datla, R.S., et al. Gene 101, 239-246 (1991). The original Bxb1 coding sequence (before A. thaliana codon optimization) was obtained from Bonnet, J. et al. Science 340, 599-603 (2013) (Genbank KC529324.1). | Vector Backbone:pBluescript II SK(-); Vector Types:Plant Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:37 | 1 | |
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INCTbiosyn-pUB-HspINT5 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127514 | Integrase 5 coding sequence codon optimized for H. sapiens expression. | Other | Ampicillin | PMID:32444777 | The integrase 5 coding sequence was synthesized and cloned into pUB-GFP plasmid (Addgene #11155) replacing the EGFP coding sequence. The original integrase coding sequence (before H. sapiens codon optimization) was obtained from Yang, L. et al. Nat. Methods 11, 1261-1266 (2014). | Vector Backbone:pUB-GFP; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:36 | 1 | |
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INCTbiosyn-pUB-HspINT4 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127513 | Integrase 4 coding sequence codon optimized for H. sapiens expression. | Other | Ampicillin | PMID:32444777 | The integrase 4 coding sequence was synthesized and cloned into pUB-GFP plasmid (Addgene #11155) replacing the EGFP coding sequence. The original integrase coding sequence (before H. sapiens codon optimization) was obtained from Yang, L. et al. Nat. Methods 11, 1261-1266 (2014). | Vector Backbone:pUB-GFP; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:36 | 1 | |
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INCTbiosyn-pUB-HspINTphiC31 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127518 | Integrase phiC31 coding sequence codon optimized for H. sapiens expression. | Other | Ampicillin | PMID:32444777 | The whole insert (promoter, CDS and terminator) was synthesized and cloned into backbone plasmid. The UbC promoter and _-globin poly(A) signal sequences are derived from pUB-GFP plasmid (Addgene #11155). | Vector Backbone:pBluescript II SK(-); Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:36 | 1 | |
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INCTbiosyn-pUB-HspINT13 Resource Report Resource Website 1+ mentions |
RRID:Addgene_127517 | Integrase 13 coding sequence codon optimized for H. sapiens expression. | Other | Ampicillin | PMID:32444777 | The integrase 13 coding sequence was synthesized and cloned into pUB-GFP plasmid (Addgene #11155) replacing the EGFP coding sequence. The original integrase coding sequence (before H. sapiens codon optimization) was obtained from Yang, L. et al. Nat. Methods 11, 1261-1266 (2014). | Vector Backbone:pUB-GFP; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:36 | 1 | |
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pSin Helper Resource Report Resource Website 1+ mentions |
RRID:Addgene_127694 | Sindbis Glycoproteins | Other | Ampicillin | PMID:31280962 | These plasmids were generated as part of the Illuminating the Druggable Genome (IDG) program sponsored by the NIH Common Fund. The goal of this program is to identify, gather, and distribute information and resources for proteins that currently are not well-studied yet belong to commonly drug-targeted protein families: protein kinases, non-olfactory G-protein coupled receptors (GPCRs), and ion channels. The IDG program is designed to develop fundamental research tools for understudied proteins, elucidate their function, and disseminate the IDG-related resources and data to the greater scientific community. | Vector Backbone:pSin; Vector Types:Synthetic Biology; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:39 | 1 | |
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pSin Capsid Resource Report Resource Website 1+ mentions |
RRID:Addgene_127693 | Sindbis Capsid | Other | Ampicillin | PMID:31280962 | These plasmids were generated as part of the Illuminating the Druggable Genome (IDG) program sponsored by the NIH Common Fund. The goal of this program is to identify, gather, and distribute information and resources for proteins that currently are not well-studied yet belong to commonly drug-targeted protein families: protein kinases, non-olfactory G-protein coupled receptors (GPCRs), and ion channels. The IDG program is designed to develop fundamental research tools for understudied proteins, elucidate their function, and disseminate the IDG-related resources and data to the greater scientific community. | Vector Backbone:pSin; Vector Types:Synthetic Biology; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:39 | 1 | |
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pSRE SSG Resource Report Resource Website 1+ mentions |
RRID:Addgene_127692 | Sindbis Structural Genome | Other | Ampicillin | PMID:31280962 | These plasmids were generated as part of the Illuminating the Druggable Genome (IDG) program sponsored by the NIH Common Fund. The goal of this program is to identify, gather, and distribute information and resources for proteins that currently are not well-studied yet belong to commonly drug-targeted protein families: protein kinases, non-olfactory G-protein coupled receptors (GPCRs), and ion channels. The IDG program is designed to develop fundamental research tools for understudied proteins, elucidate their function, and disseminate the IDG-related resources and data to the greater scientific community. | Vector Backbone:pSRE; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:04:38 | 2 | |
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pLenti c-MYC-DDK-Puro GFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_123299 | GFP | Other | Chloramphenicol | PMID:30373810 | Vector Backbone:pLenti-C-MYC-DDK Puro; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Chloramphenicol | 2026-08-15 01:03:53 | 1 | ||
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pAAV-Syn-ChromeQ-GFP Resource Report Resource Website |
RRID:Addgene_123317 | ChromeQ-GFP | Other | Ampicillin | PMID:30610117 | The plasmid is fully sequenced in the coding sequence regions (opsin-fluorophore and important flanking regions). Multiple digestions were done to verify the vector structure. The construct and the virus were both tested in vitro. | Backbone Marker:original from Stratagene; Backbone Size:4708; Vector Backbone:pAAV-Syn; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin | Channelrhodopsin-2 (ChR2) with mutations A71S/ E90A/H114G/R115S | 2026-08-15 01:03:53 | 0 |
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pLPhygSaCas9 Resource Report Resource Website |
RRID:Addgene_123262 | Staphylococcus aureus Cas9 | Other | Ampicillin | PMID:31434745 | Vector Backbone:pSP72; Vector Types:CRISPR, Leishmania; Bacterial Resistance:Ampicillin | 2026-08-15 01:03:52 | 0 | ||
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pMK-PpsbB Resource Report Resource Website |
RRID:Addgene_123481 | PpsbB | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK-RQ; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 | |
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pMK-PpsbD-leader Resource Report Resource Website |
RRID:Addgene_123482 | PpsbD-leader | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK-T; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 | |
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pMK-PrbcL Resource Report Resource Website |
RRID:Addgene_123485 | PrbcL | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK-T; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 | |
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pMK-PrbcL (-110 to +9) Resource Report Resource Website |
RRID:Addgene_123487 | PrbcL (-110 to +9) | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 | |
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pMK-PrbcL (core -35 to +9) Resource Report Resource Website |
RRID:Addgene_123486 | PrbcL (core -35 to +9) | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK-RQ; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 | |
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pMK-Prrn16 Resource Report Resource Website |
RRID:Addgene_123489 | Prrn16 | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK-RQ; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 | |
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pMK-mPrrn::RBS (60%) Resource Report Resource Website |
RRID:Addgene_123517 | mPrrn::RBS (60%) | Other | Kanamycin | PMID:30679266 | All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast promoter::5'UTR fusion designed for Golden-Gate cloning. The Original Material was developed in the performance of research that was funded by Grant Nos. ARPA-E: DE-AR000660 & DARPA: D17AC00016. | Vector Backbone:pMK; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin | 2026-08-15 01:03:55 | 0 |
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