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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
Comments |
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P-rTetO-mCherry-T2A-RPL22-1xV5 Resource Report Resource Website |
RRID:Addgene_170325 | RPL22 | Homo sapiens | Ampicillin | PMID:32516938 | Vector Backbone:pLV; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | None | 2026-08-15 01:10:07 | 0 | |
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P-rTetO-EGFP-T2A-RPL22-3xHA Resource Report Resource Website |
RRID:Addgene_170326 | RPL22 | Homo sapiens | Ampicillin | PMID:32516938 | Vector Backbone:pLV; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | None | 2026-08-15 01:10:07 | 0 | |
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pcDNA3.3_CoV1_D28 Resource Report Resource Website 10+ mentions |
RRID:Addgene_170447 | SARS-CoV-1 spike D28 | SARS-CoV-1 | Ampicillin | PMID:32540903 | Backbone Size:5500; Vector Backbone:pcDNA3.3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | last 28aa deletion in c-terminal tail | 2026-08-15 01:10:08 | 11 | |
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pCDH-EF1a-hLMX1A-T2A-copGFP Resource Report Resource Website |
RRID:Addgene_170444 | human LMX1A | Ampicillin | PMID:33597231 | Backbone Marker:System Biosciences; Backbone Size:7424; Vector Backbone:pCDH-EF1a-T2A-copGFP; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:08 | 0 | |||
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P-Ef1a-mCherry-T2A-RPL22-1xV5 Resource Report Resource Website |
RRID:Addgene_170324 | RPL22 | Homo sapiens | Ampicillin | PMID:32516938 | Vector Backbone:pFUGW; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | None | 2026-08-15 01:10:07 | 0 | |
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pPD152.79 Resource Report Resource Website |
RRID:Addgene_1704 | Ampicillin | See Fire Lab Vector Kit Documentation 2005. Fire Lab Miniprep Number pPD152.79, Ligation number L5494. | Backbone Size:4771; Vector Types:Worm Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:07 | 0 | ||||
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pESUMO-hRORg2 Resource Report Resource Website 1+ mentions |
RRID:Addgene_170329 | RORG isoform 2 | Homo sapiens | Ampicillin | PMID:34547329 | Backbone Marker:LifeSensor; Backbone Size:5476; Vector Backbone:pESUMO; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | codon optimized | 2026-08-15 01:10:07 | 1 | |
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pET-DEST42-dre4 Resource Report Resource Website |
RRID:Addgene_170440 | dre4 | Drosophila melanogaster | Ampicillin | PMID:31242411 | The expressed his-tagged protein, pET-DEST42-dre4 (deleted amino acids 1-20) was efficiently bound to CNBR beads during the affinity purification of the antibodies. | Backbone Marker:Invitrogen; Backbone Size:7440; Vector Backbone:pET-DEST42; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | Deleted amino acids 1-20 | 2026-08-15 01:10:08 | 0 |
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pAC-CR7T-gRNA2.1-nlsBFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_170515 | Ampicillin | PMID:33782117 | For more information about the Han Lab Drosophila Transgenic Vectors, please visit: https://han.wicmb.cornell.edu/han-lab-drosophila-transgenic-vectors/ | Backbone Size:12778; Vector Backbone:pAC; Vector Types:Insect Expression, CRISPR; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:08 | 1 | |||
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LentiGuide Cherry Resource Report Resource Website 1+ mentions |
RRID:Addgene_170510 | S. pyogenes sgRNA cassette | Synthetic | Ampicillin | Plasmid based on lentiGuide Puro (addgene plasmid #52963). Please visit https://www.biorxiv.org/content/10.1101/2021.03.02.433398v1 for bioRxiv preprint. | Backbone Marker:Feng Zhang lab (Addgene plasmid #52963); Vector Backbone:lentiGuide-Puro; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:08 | 2 | ||
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p663-UBC-miniTurbo-V5-PIP4K2C_IDG-K Resource Report Resource Website |
RRID:Addgene_170598 | miniTurbo-V5-PIP4K2C | 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. These lentiviral gateway destination plasmids were generated, as part of the Kinase-Data and Resource Generating Center (DRGC), using the single fragment or multisite gateway cloning technology. They were used for generating proteomics-based protein-interaction and protein-proximity networks that can be accessed through the kinase-DRGC website https://darkkinome.org/. Each plasmid has either an N- or C-terminal fusion protein (Flag/ V5/V5-miniTurbo/V5-TurboID/miniTurbo-V5/TurboID-V5) tagged understudied kinase driven under either a CMV or Ubiquitin (UBC) promoter. All inserts in the pENTR plasmids used to generate the deposited destination plasmids were end-sequenced and insert size validated prior to multi-site gateway cloning. The combined insert size of the single fragment or three fragment destination plasmids were confirmed by restriction digestion (BsrGI, and EcoRV for pDest667; BsrGI, EcoRV, and BstZ17I for pDest663; and BsrGI for pHAGE) and all plasmids were partially sequenced to ensure in-frame ORFs and fusion tags. | Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:09 | 0 | ||
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p663-UBC-miniTurbo-V5-PIP5K1B_IDG-K Resource Report Resource Website |
RRID:Addgene_170599 | miniTurbo-V5-PIP5K1B | 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. These lentiviral gateway destination plasmids were generated, as part of the Kinase-Data and Resource Generating Center (DRGC), using the single fragment or multisite gateway cloning technology. They were used for generating proteomics-based protein-interaction and protein-proximity networks that can be accessed through the kinase-DRGC website https://darkkinome.org/. Each plasmid has either an N- or C-terminal fusion protein (Flag/ V5/V5-miniTurbo/V5-TurboID/miniTurbo-V5/TurboID-V5) tagged understudied kinase driven under either a CMV or Ubiquitin (UBC) promoter. All inserts in the pENTR plasmids used to generate the deposited destination plasmids were end-sequenced and insert size validated prior to multi-site gateway cloning. The combined insert size of the single fragment or three fragment destination plasmids were confirmed by restriction digestion (BsrGI, and EcoRV for pDest667; BsrGI, EcoRV, and BstZ17I for pDest663; and BsrGI for pHAGE) and all plasmids were partially sequenced to ensure in-frame ORFs and fusion tags. | Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:09 | 0 | ||
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p663-UBC-miniTurbo-V5-PIK3C2G_IDG-K Resource Report Resource Website |
RRID:Addgene_170597 | miniTurbo-V5-PIK3C2G | 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. These lentiviral gateway destination plasmids were generated, as part of the Kinase-Data and Resource Generating Center (DRGC), using the single fragment or multisite gateway cloning technology. They were used for generating proteomics-based protein-interaction and protein-proximity networks that can be accessed through the kinase-DRGC website https://darkkinome.org/. Each plasmid has either an N- or C-terminal fusion protein (Flag/ V5/V5-miniTurbo/V5-TurboID/miniTurbo-V5/TurboID-V5) tagged understudied kinase driven under either a CMV or Ubiquitin (UBC) promoter. All inserts in the pENTR plasmids used to generate the deposited destination plasmids were end-sequenced and insert size validated prior to multi-site gateway cloning. The combined insert size of the single fragment or three fragment destination plasmids were confirmed by restriction digestion (BsrGI, and EcoRV for pDest667; BsrGI, EcoRV, and BstZ17I for pDest663; and BsrGI for pHAGE) and all plasmids were partially sequenced to ensure in-frame ORFs and fusion tags. | Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:10 | 0 | ||
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ZE11 tiggywinkle hedgehog CMV Resource Report Resource Website |
RRID:Addgene_17060 | tiggywinkle hedgehog | Danio rerio | Ampicillin | twhh under control of CMV promoter. | Backbone Size:0; Vector Backbone:NA; Vector Types:; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:09 | 0 | ||
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pXL-BacII-CAG-mCherry Resource Report Resource Website |
RRID:Addgene_170519 | CAG-mCherry | Synthetic | Ampicillin | PMID:34458399 | More information can be found in this additional reference: Yamagata M, Yan W, Sanes JR. A cell atlas of the chick retina based on single-cell transcriptomics. Elife. 2021 Jan 4;10:e63907. doi: 10.7554/eLife.63907. PMID: 33393903; PMCID: PMC7837701. | Vector Backbone:pXL-BacII; Vector Types:Mammalian Expression, piggyBAC transposon; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:08 | 0 | |
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ZE19 wnt8 pBand3-5 Resource Report Resource Website |
RRID:Addgene_17053 | wnt8 pBand3-5 | Danio rerio | Ampicillin | PMID:11703928 | RT PCR prodct ligated into vector full length cDNA cloned includes ORF1, IRES and ORF2. For antiense RNA: transcribe with SP6 polymerase. Plasmid History: Species of Sequence Origin: Zebrafish. Reference: Lekven, Dev Cell, 2001. | Backbone Marker:Promega; Backbone Size:3000; Vector Backbone:pGemT easy; Vector Types:; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:08 | 0 | |
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ZE7 Pax2 Resource Report Resource Website |
RRID:Addgene_17056 | pax b | Danio rerio | Ampicillin | PMID:7586754 | Insert: pax b sense or antisense orientation. Insert size: 1.18 Kb. Transcription: linearize at EcoR1, transcribe with SP6. Plasmid History: Constructed by Greg Kelly on date of 9/21/92, page 118 Book 1. Sepecies of Sequence Origin: Zebrafish. Note for Use: This construct is used to make DIG probes or for making RNA suitable for injections. Citation: Kelly and Moon, Developmental Genetics (1995) | Backbone Size:3000; Vector Backbone:SP64T; Vector Types:Zebrafish Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:09 | 0 | |
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p663-UBC-miniTurbo-V5-MKNK2_IDG-K Resource Report Resource Website |
RRID:Addgene_170594 | miniTurbo-V5-MKNK2 | 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. These lentiviral gateway destination plasmids were generated, as part of the Kinase-Data and Resource Generating Center (DRGC), using the single fragment or multisite gateway cloning technology. They were used for generating proteomics-based protein-interaction and protein-proximity networks that can be accessed through the kinase-DRGC website https://darkkinome.org/. Each plasmid has either an N- or C-terminal fusion protein (Flag/ V5/V5-miniTurbo/V5-TurboID/miniTurbo-V5/TurboID-V5) tagged understudied kinase driven under either a CMV or Ubiquitin (UBC) promoter. All inserts in the pENTR plasmids used to generate the deposited destination plasmids were end-sequenced and insert size validated prior to multi-site gateway cloning. The combined insert size of the single fragment or three fragment destination plasmids were confirmed by restriction digestion (BsrGI, and EcoRV for pDest667; BsrGI, EcoRV, and BstZ17I for pDest663; and BsrGI for pHAGE) and all plasmids were partially sequenced to ensure in-frame ORFs and fusion tags. | Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:10 | 0 | ||
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p663-UBC-miniTurbo-V5-EEF2K_IDG-K Resource Report Resource Website |
RRID:Addgene_170592 | miniTurbo-V5-EEF2K | 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. These lentiviral gateway destination plasmids were generated, as part of the Kinase-Data and Resource Generating Center (DRGC), using the single fragment or multisite gateway cloning technology. They were used for generating proteomics-based protein-interaction and protein-proximity networks that can be accessed through the kinase-DRGC website https://darkkinome.org/. Each plasmid has either an N- or C-terminal fusion protein (Flag/ V5/V5-miniTurbo/V5-TurboID/miniTurbo-V5/TurboID-V5) tagged understudied kinase driven under either a CMV or Ubiquitin (UBC) promoter. All inserts in the pENTR plasmids used to generate the deposited destination plasmids were end-sequenced and insert size validated prior to multi-site gateway cloning. The combined insert size of the single fragment or three fragment destination plasmids were confirmed by restriction digestion (BsrGI, and EcoRV for pDest667; BsrGI, EcoRV, and BstZ17I for pDest663; and BsrGI for pHAGE) and all plasmids were partially sequenced to ensure in-frame ORFs and fusion tags. | Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:09 | 0 | ||
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p663-UBC-miniTurbo-V5-MKNK1_IDG-K Resource Report Resource Website |
RRID:Addgene_170593 | miniTurbo-V5-MKNK1 | 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. These lentiviral gateway destination plasmids were generated, as part of the Kinase-Data and Resource Generating Center (DRGC), using the single fragment or multisite gateway cloning technology. They were used for generating proteomics-based protein-interaction and protein-proximity networks that can be accessed through the kinase-DRGC website https://darkkinome.org/. Each plasmid has either an N- or C-terminal fusion protein (Flag/ V5/V5-miniTurbo/V5-TurboID/miniTurbo-V5/TurboID-V5) tagged understudied kinase driven under either a CMV or Ubiquitin (UBC) promoter. All inserts in the pENTR plasmids used to generate the deposited destination plasmids were end-sequenced and insert size validated prior to multi-site gateway cloning. The combined insert size of the single fragment or three fragment destination plasmids were confirmed by restriction digestion (BsrGI, and EcoRV for pDest667; BsrGI, EcoRV, and BstZ17I for pDest663; and BsrGI for pHAGE) and all plasmids were partially sequenced to ensure in-frame ORFs and fusion tags. | Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:09 | 0 |
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