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Plasmids are provided by Addgene and DGRC.

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On page 425 showing 8481 ~ 8500 out of 69,655 results
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  • RRID:Addgene_193162

http://www.addgene.org/193162

Species: Homo sapiens
Genetic Insert: Barcoded piggyBac Puro SRT
Vector Backbone Description: Vector Backbone:PB-SRT-Puro; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36062164

Proper citation: RRID:Addgene_193162 Copy   


  • RRID:Addgene_193163

http://www.addgene.org/193163

Species: Homo sapiens
Genetic Insert: Barcoded piggyBac Puro SRT
Vector Backbone Description: Vector Backbone:PB-SRT-Puro; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36062164

Proper citation: RRID:Addgene_193163 Copy   


http://www.addgene.org/213722

Species: Homo sapiens
Genetic Insert: EGFP
Vector Backbone Description: Vector Backbone:pcDNA3.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36250010

Proper citation: RRID:Addgene_213722 Copy   


  • RRID:Addgene_213587

http://www.addgene.org/213587

Species: Homo sapiens
Genetic Insert: TAZ
Vector Backbone Description: Backbone Size:12153; Vector Backbone:p-Inducer10b; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37934103

Proper citation: RRID:Addgene_213587 Copy   


  • RRID:Addgene_213588

http://www.addgene.org/213588

Species: Homo sapiens
Genetic Insert: TAZ
Vector Backbone Description: Backbone Size:12153; Vector Backbone:p-Inducer10b; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37934103

Proper citation: RRID:Addgene_213588 Copy   


http://www.addgene.org/213589

Species: Homo sapiens
Genetic Insert: TAZ
Vector Backbone Description: Backbone Size:12153; Vector Backbone:p-Inducer10b; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37934103

Proper citation: RRID:Addgene_213589 Copy   


  • RRID:Addgene_213583

http://www.addgene.org/213583

Species: Homo sapiens
Genetic Insert: YAP1
Vector Backbone Description: Backbone Size:12153; Vector Backbone:p-Inducer10b; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37934103

Proper citation: RRID:Addgene_213583 Copy   


http://www.addgene.org/213585

Species: Homo sapiens
Genetic Insert: YAP1
Vector Backbone Description: Backbone Size:12153; Vector Backbone:p-Inducer10b; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37934103

Proper citation: RRID:Addgene_213585 Copy   


http://www.addgene.org/213590

Species: Homo sapiens
Genetic Insert: TAZ
Vector Backbone Description: Backbone Size:12153; Vector Backbone:p-Inducer10b; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37934103

Proper citation: RRID:Addgene_213590 Copy   


  • RRID:Addgene_214440

http://www.addgene.org/214440

Species: Homo sapiens
Genetic Insert: CBLB:PBC020-G02:C248501
Vector Backbone Description: Vector Backbone:pET28-MHL (Addgene #26096); Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Comments: PBD link: https://www.rcsb.org/structure/8GCY

Proper citation: RRID:Addgene_214440 Copy   


  • RRID:Addgene_214734

    This resource has 1+ mentions.

http://www.addgene.org/214734

Species: Homo sapiens
Genetic Insert: CAG_iPE-N_bGH
Vector Backbone Description: Backbone Size:2828; Vector Backbone:pBlueScript; Vector Types:Mammalian Expression, CRISPR, Synthetic Biology; Bacterial Resistance:Ampicillin
Defining Citation: PMID:38302659

Proper citation: RRID:Addgene_214734 Copy   


  • RRID:Addgene_214735

    This resource has 1+ mentions.

http://www.addgene.org/214735

Species: Homo sapiens
Genetic Insert: CAG_iPE-C_bGH
Vector Backbone Description: Backbone Size:2825; Vector Backbone:pBlueScript; Vector Types:Mammalian Expression, CRISPR, Synthetic Biology; Bacterial Resistance:Ampicillin
Defining Citation: PMID:38302659

Proper citation: RRID:Addgene_214735 Copy   


http://www.addgene.org/214471

Species: Homo sapiens
Genetic Insert: ZFYVE27
Vector Backbone Description: Vector Backbone:pHRsinUbEm; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin

Proper citation: RRID:Addgene_214471 Copy   


http://www.addgene.org/213717

Species: Homo sapiens
Genetic Insert: EGFP
Vector Backbone Description: Vector Backbone:pLKO.1; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36250010

Proper citation: RRID:Addgene_213717 Copy   


  • RRID:Addgene_209075

http://www.addgene.org/209075

Species: Homo sapiens
Genetic Insert: PRF1-Exon3 HDRT
Vector Backbone Description: Backbone Size:3155; Vector Backbone:pDonor; Vector Types:CRISPR; Bacterial Resistance:Ampicillin
Defining Citation: PMID:38306418

Proper citation: RRID:Addgene_209075 Copy   


http://www.addgene.org/214460

Species: Homo sapiens
Genetic Insert: miniTurbo-V5-CSNK1G3
Vector Backbone Description: Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin
Comments: 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.

Proper citation: RRID:Addgene_214460 Copy   


http://www.addgene.org/214463

Species: Homo sapiens
Genetic Insert: miniTurbo-V5-PRPF4B
Vector Backbone Description: Backbone Marker:PEL; Backbone Size:9019; Vector Backbone:pDest663; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin
Comments: 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.

Proper citation: RRID:Addgene_214463 Copy   


http://www.addgene.org/214466

Species: Homo sapiens
Genetic Insert: STK17A-V5-miniTurbo
Vector Backbone Description: Backbone Marker:PEL; Backbone Size:9014; Vector Backbone:pDest667; Vector Types:Mammalian Expression, Lentiviral, Gateway Destination; Bacterial Resistance:Ampicillin
Comments: 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.

Proper citation: RRID:Addgene_214466 Copy   


http://www.addgene.org/166910

Species: Homo sapiens
Genetic Insert: ARNT shRNA
Vector Backbone Description: Backbone Size:11000; Vector Backbone:pLKO-TET-ON-addgene#21915; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:37620297

Proper citation: RRID:Addgene_166910 Copy   


http://www.addgene.org/214919

Species: Homo sapiens
Genetic Insert: SRRD
Vector Backbone Description: Vector Backbone:pLEX_307; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin
Defining Citation: PMID:38315730

Proper citation: RRID:Addgene_214919 Copy   



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