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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
Comments |
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|---|---|---|---|---|---|---|---|---|---|---|
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pET28a-Ec.coaA Resource Report Resource Website 1+ mentions |
RRID:Addgene_50386 | PanK | E coli | Kanamycin | PMID:15795230 | Backbone Marker:Novagen; Vector Backbone:pET28a; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin | 2026-08-15 01:16:05 | 3 | ||
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pET28a-Ec.coaE (pESC124) Resource Report Resource Website 1+ mentions |
RRID:Addgene_50390 | DPCK | E coli | Kanamycin | PMID:12372838 | Backbone Marker:Novagen; Vector Backbone:pET28a; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin | 2026-08-15 01:16:05 | 1 | ||
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pICSL50010 Resource Report Resource Website 1+ mentions |
RRID:Addgene_50310 | C terminal Myc tag (4x Myc) | Other | Spectinomycin | PMID:24933124 | insert can be released with BsaI | Vector Backbone:PAGM1301; Vector Types:plant expression; Bacterial Resistance:Spectinomycin | BsaI/BbsI sites removed by point-mutation | 2026-08-15 01:16:04 | 3 |
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pLenti6.3-hEPO Resource Report Resource Website 1+ mentions |
RRID:Addgene_50436 | EPO | Homo sapiens | Ampicillin | PMID:21937702 | Human erythropoietin (hEPO) ORF with stop codon (582 bp; Ultimate ORF clone number IOH7334) from GeneCopoeia ORF cDNA clones in pDONR vector (GeneCopoeia; GC-A1011). Because the stop codon is inserted before V5 epitope, the V5 tag on the pLenti6.3/V5-DEST vector won’t be transcribed. | Backbone Marker:Invitrogen; Backbone Size:9387; Vector Backbone:pLenti6.3/V5-DEST gateway vector; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:05 | 2 | |
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pAAV-hSyn-DIO-mCherry Resource Report Resource Website 100+ mentions |
RRID:Addgene_50459 | mCherry | Aequorea victoria | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:08 | 388 | ||
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pAAV-hSyn-DIO-rM3D(Gs)-mCherry Resource Report Resource Website 10+ mentions |
RRID:Addgene_50458 | rM3D-mCherry | Rattus norvegicus | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 12 | |
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pAAV-hSyn-DIO-HA-hM4D(Gi)-IRES-mCitrine Resource Report Resource Website 10+ mentions |
RRID:Addgene_50455 | hM4D(Gi)-IRES-mCitrine | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 19 | |
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pAAV-hSyn-DIO-HA-hM3D(Gq)-IRES-mCitrine Resource Report Resource Website 10+ mentions |
RRID:Addgene_50454 | hM3D(Gq)-IRES-mCitrine | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:05 | 14 | |
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pAAV-hSyn-DIO-EGFP Resource Report Resource Website 100+ mentions |
RRID:Addgene_50457 | EGFP | Aequorea victoria | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:06 | 127 | ||
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pAAV-EF1a-DIO-mCherry Resource Report Resource Website 10+ mentions |
RRID:Addgene_50462 | mCherry | Aequorea victoria | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:08 | 34 | ||
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pAAV-hSyn-HA-hM4D(Gi)-IRES-mCitrine Resource Report Resource Website 1+ mentions |
RRID:Addgene_50464 | hM4D(Gi)-IRES-mCitrine | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:06 | 9 | ||
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pAAV-hSyn-HA-hM3D(Gq)-IRES-mCitrine Resource Report Resource Website 1+ mentions |
RRID:Addgene_50463 | hM3D(Gq)-IRES-mCitrine | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 7 | |
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pAAV-EF1a-DIO-hM3D(Gq)-mCherry Resource Report Resource Website 10+ mentions |
RRID:Addgene_50460 | hM3D(Gq)-mCherry | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 29 | |
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pAAV-CaMKIIa-EGFP Resource Report Resource Website 50+ mentions |
RRID:Addgene_50469 | EGFP | Aequorea victoria | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:06 | 74 | ||
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pAAV-hSyn-EGFP Resource Report Resource Website 100+ mentions |
RRID:Addgene_50465 | EGFP | Aequorea victoria | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:08 | 223 | ||
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pAAV-CaMKIIa-HA-rM3D(Gs)-IRES-mCitrine Resource Report Resource Website 1+ mentions |
RRID:Addgene_50468 | rM3D-IRES-mCitrine | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:08 | 2 | ||
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pAAV-GFAP-EGFP Resource Report Resource Website 10+ mentions |
RRID:Addgene_50473 | EGFP | Aequorea victoria | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | 2026-08-15 01:16:06 | 25 | ||
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pAAV-GFAP-HA-rM3D(Gs)-IRES-mCitrine Resource Report Resource Website 1+ mentions |
RRID:Addgene_50472 | rM3D-IRES-mCitrine | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 7 | |
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pAAV-hSyn-hM4D(Gi)-mCherry Resource Report Resource Website 100+ mentions |
RRID:Addgene_50475 | hM4D(Gi)-mCherry | Ampicillin | Please Note- This plasmid does NOT contain an N-terminal HA tag. 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 116 | ||
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pAAV-GFAP-HA-hM3D(Gq)-IRES-mCitrine Resource Report Resource Website 1+ mentions |
RRID:Addgene_50470 | hM3D(Gq)-IRES-mCitrine | Homo sapiens | Ampicillin | 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. | Backbone Size:4818; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin | See supplemental documents for DREADD mutations | 2026-08-15 01:16:06 | 1 |
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