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Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123000 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123002 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123004 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123007 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123008 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123023 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123010 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123011 Copy
Species: Other
Genetic Insert: chaperonin-60 universal target
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pGEM-T Easy; Vector Types:molecular diagnostic assay control; Bacterial Resistance:Ampicillin
Comments: Cloning method is T-vector cloning of a PCR product
Proper citation: RRID:Addgene_123017 Copy
Species: Other
Genetic Insert: ChromeQ-mCherry
Vector Backbone Description: Backbone Marker:stratagene; Backbone Size:4915; Vector Backbone:pAAV-GFAP104; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30610117
Comments: 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.
Proper citation: RRID:Addgene_123125 Copy
Species: Other
Genetic Insert: LacZ
Vector Backbone Description: Vector Backbone:pEF-DEST51; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30373810
Proper citation: RRID:Addgene_123292 Copy
Species: Other
Genetic Insert: ChromeT-GFP
Vector Backbone Description: Backbone Marker:original from Stratagene; Backbone Size:4708; Vector Backbone:pAAV-Syn; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30610117
Comments: 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.
Proper citation: RRID:Addgene_123316 Copy
Species: Other
Genetic Insert: Non-targeting shRNA
Vector Backbone Description: Vector Backbone:pLKO.1 Puro; Vector Types:Lentiviral, RNAi; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30373810
Proper citation: RRID:Addgene_123306 Copy
Species: Other
Genetic Insert: PpsbA (-42 to +9)
Vector Backbone Description: Vector Backbone:pMK-T; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: 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.
Proper citation: RRID:Addgene_123480 Copy
Species: Other
Genetic Insert: PpsbD-PGTbx
Vector Backbone Description: Vector Backbone:pMK-T; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: 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.
Proper citation: RRID:Addgene_123483 Copy
Species: Other
Genetic Insert: PpsbD
Vector Backbone Description: Vector Backbone:pMK-T; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: 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.
Proper citation: RRID:Addgene_123484 Copy
Species: Other
Genetic Insert: atpB 5'UTR
Vector Backbone Description: Vector Backbone:pMK-RQ; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast 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.
Proper citation: RRID:Addgene_123520 Copy
Species: Other
Genetic Insert: PrpoB
Vector Backbone Description: Vector Backbone:pMK-RQ; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: 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.
Proper citation: RRID:Addgene_123488 Copy
Species: Other
Genetic Insert: atpB 5'UTR +10 (functional)
Vector Backbone Description: Vector Backbone:pMK-RQ; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: All inserts have been produced by gene synthesis and cloned in the indicated backbone vector. The insert is a chloroplast 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.
Proper citation: RRID:Addgene_123521 Copy
Species: Other
Genetic Insert: mPrrn::RBS (46%)
Vector Backbone Description: Vector Backbone:pMK; Vector Types:Synthetic Biology; Bacterial Resistance:Kanamycin
Defining Citation: PMID:30679266
Comments: 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.
Proper citation: RRID:Addgene_123516 Copy
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