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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
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w+attB Resource Report Resource Website 10+ mentions |
RRID:Addgene_30326 | phiC31 attB, hsp70::w | Drosophila melanogaster | Ampicillin | w[+] is hsp70 basal promoter; gives full w+ (red eyes), without heat shock. | Backbone Size:2881; Vector Backbone:pUC; Vector Types:Drosophila transgenesis; Bacterial Resistance:Ampicillin | 2026-08-15 01:13:24 | 12 | ||
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gstops Resource Report Resource Website |
RRID:Addgene_26859 | Slow Termination of Phototransduction | Drosophila melanogaster | Ampicillin | PMID:18184564 | Backbone Size:7855; Vector Backbone:pCaspeR4; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:57 | 0 | ||
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ninaE-stops myc Resource Report Resource Website |
RRID:Addgene_26856 | Slow Termination of Phototransduction | Drosophila melanogaster | Ampicillin | PMID:18184564 | To express the stops cDNA under the control of the ninaE promoter, the cDNA (EST clone GH07253, DGRC) was subcloned between the NotI and XbaI sites of pCNX. To express Myc-tagged wild-type STOPS in flies, the sequence encoding a Myc tag was fused to the 3' end of the wild-type stops cDNA. The wild-type stops cDNAs was subsequently subcloned between the NotI and XbaI sites of pCNX. The pCNX vector was constructed as follows. First, the pNX vector (provided by Dr. J. O'Tousa, University of Notre Dame, Notre Dame, IN) was digested with KpnI and NotI, which liberated a 3 kb ninaE promoter sequence, and this fragment was subsequently introduced between the same sites of pCaspeR4. Second, to provide the signals for polyadenylation and 3' end cleavage of RNAs, a simian virus 40 3' region (0.5 kb) was excised from pCaspeR–heat shock protein 70 promoter (hs) and introduced between the XbaI and XhoI sites of the vector | Backbone Size:0; Vector Backbone:pCNX; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:57 | 0 | |
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ninaE-stops m3-myc Resource Report Resource Website |
RRID:Addgene_26855 | Slow Termination of Phototransduction | Drosophila melanogaster | Ampicillin | PMID:18184564 | To express the stops cDNA under the control of the ninaE promoter, the cDNA (EST clone GH07253, DGRC) was subcloned between the NotI and XbaI sites of pCNX. To express Myc-tagged wild-type STOPS in flies, the sequence encoding a Myc tag was fused to the 3' end of the wild-type stops cDNA. The wild-type stops cDNAs was subsequently subcloned between the NotI and XbaI sites of pCNX. The pCNX vector was constructed as follows. First, the pNX vector (provided by Dr. J. O'Tousa, University of Notre Dame, Notre Dame, IN) was digested with KpnI and NotI, which liberated a 3 kb ninaE promoter sequence, and this fragment was subsequently introduced between the same sites of pCaspeR4. Second, to provide the signals for polyadenylation and 3' end cleavage of RNAs, a simian virus 40 3' region (0.5 kb) was excised from pCaspeR–heat shock protein 70 promoter (hs) and introduced between the XbaI and XhoI sites of the vector | Backbone Size:0; Vector Backbone:pCNX; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | Amino acids 296-299 (SLRH in wild-type) are mutated to GPGD | 2026-08-15 01:12:57 | 0 |
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ninaE-dsocs Resource Report Resource Website |
RRID:Addgene_26857 | Slow Termination of Phototransduction | Drosophila melanogaster | Ampicillin | PMID:18184564 | To express the stops cDNA under the control of the ninaE promoter, the cDNA (EST clone GH07253, DGRC) was subcloned between the NotI and XbaI sites of pCNX. Myc-tagged STOPS lacking the SOCS box was subcloned between the NotI and XbaI sites of pCNX. The pCNX vector was constructed as follows. First, the pNX vector (provided by Dr. J. O'Tousa, University of Notre Dame, Notre Dame, IN) was digested with KpnI and NotI, which liberated a 3 kb ninaE promoter sequence, and this fragment was subsequently introduced between the same sites of pCaspeR4. Second, to provide the signals for polyadenylation and 3' end cleavage of RNAs, a simian virus 40 3' region (0.5 kb) was excised from pCaspeR–heat shock protein 70 promoter (hs) and introduced between the XbaI and XhoI sites of the vector | Backbone Size:0; Vector Backbone:pCNX; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | This STOPS construct contains a mutated/truncated SOCS box (suppressor of cytokine signaling). Amino acids 296 and 297 have been mutated from SL to EF and amino acids 298-330 have been deleted | 2026-08-15 01:12:57 | 0 |
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ninaE-norpA Resource Report Resource Website |
RRID:Addgene_26854 | no receptor potential A | Drosophila melanogaster | Ampicillin | PMID:18184564 | To express norpA under control of the ninaE promoter, full length norpA cDNA was excised from pHKX-norpA and subcloned into pCNX | Backbone Size:0; Vector Backbone:pCNX; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | V963A | 2026-08-15 01:12:57 | 0 |
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pUAS myc Gr66a Resource Report Resource Website |
RRID:Addgene_26861 | Gr66 gustatory receptor | Drosophila melanogaster | Ampicillin | PMID:16979558 | Backbone Size:0; Vector Backbone:pP[UAS-myc]; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:57 | 0 | ||
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pcasper4 p [7-Gr66a-] Resource Report Resource Website |
RRID:Addgene_26860 | Gr66 gustatory receptor | Drosophila melanogaster | Ampicillin | PMID:16979558 | Backbone Size:7855; Vector Backbone:pCaSper4; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | Partial deletion of Gr66a (see associated paper listed below for details), but contains genes CG7066 and CG7188, which neighbor Gr66a | 2026-08-15 01:12:57 | 0 | |
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pRmHa3-dKDM4A-HA2FL2 Resource Report Resource Website |
RRID:Addgene_20232 | dKDM4A | Drosophila melanogaster | Ampicillin | PMID:19061644 | Backbone Size:3990; Vector Backbone:pRmHa3-CHA2FL2; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:11:53 | 0 | ||
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pRmHa3-dKDM4A-H195A-HA2FL2 Resource Report Resource Website |
RRID:Addgene_20235 | dKDM4A | Drosophila melanogaster | Ampicillin | PMID:19061644 | D153E mutation is also present, but it does affect the plasmid. | Backbone Size:3990; Vector Backbone:pRmHa3-CHA2FL2; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | changed His 195 to Ala | 2026-08-15 01:11:53 | 0 |
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pBacPAK-HFT-dKDM4B Resource Report Resource Website |
RRID:Addgene_20234 | dKDM4B | Drosophila melanogaster | Ampicillin | PMID:19061644 | TEV tag ENPYFQG instead of ENLYFQG. The cDNA used in making dKDM4B(CG33182) constructs has incomplete 3' end. It is because NCBI data has updated the sequence after I made the construct. There is a comment on NCBI page https://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=161077032&from=148&to=1920&view=gbwithparts indicates that they replaced a former sequence of CG33182 https://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=28573833 with the current 1773bp one. | Backbone Size:5608; Vector Backbone:pBacPAK-HFT; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:11:53 | 0 | |
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pBacPAK-HFT-dKDM4A Resource Report Resource Website |
RRID:Addgene_20233 | dKDM4A | Drosophila melanogaster | Ampicillin | PMID:19061644 | TEV tag ENPYFQG instead of ENLYFQG. | Backbone Size:5608; Vector Backbone:pBacPAK-HFT; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:11:53 | 0 | |
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pBS-Squ:mCherry Resource Report Resource Website 1+ mentions |
RRID:Addgene_20163 | spaghetti squash (squ, myosin II RLC) 5' UTR and ORF fused to mCherry followed by squ 3' UTR | Drosophila melanogaster | Ampicillin | PMID:19029882 | There are several polymorphisms in the 3’UTR of the expression construct and should not affect the function. | Backbone Size:3000; Vector Backbone:pBluescript; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:11:52 | 1 | |
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pUAST-Gr64d Resource Report Resource Website |
RRID:Addgene_21079 | Gr64d | Drosophila melanogaster | Ampicillin | PMID:19026541 | Backbone Size:11000; Vector Backbone:pUAST; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:11:59 | 0 | ||
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pUAST-Gr64a Resource Report Resource Website |
RRID:Addgene_21081 | Gr64a | Drosophila melanogaster | Ampicillin | PMID:17715294 | Backbone Size:11000; Vector Backbone:pUAST; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:11:59 | 0 | ||
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pMT-Pav-GFP Resource Report Resource Website |
RRID:Addgene_24286 | Pavarotti | Drosophila melanogaster | Ampicillin | PMID:19720876 | This plasmid was originally generated by Dr. Gohta Goshima and published in MBOC. Vol. 16, 3896–3907. | Backbone Marker:Invitrogen; Backbone Size:4200; Vector Backbone:pMT-GFP; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:29 | 0 | |
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pMT-GFP-p150Dynactin Resource Report Resource Website |
RRID:Addgene_24283 | p150 Dynactin | Drosophila melanogaster | Ampicillin | PMID:17576797 | Dr. Goshima made a C-terminal GFP p150 plasmid and Vale lab used his pENTR vector to make an N-terminal fusion using Gateway cloning. Y1238H mutation detected in Addgene's BGH-rev sequence is not likely to affect function. | Backbone Marker:Drosophila Gateway Vector Collection; Backbone Size:5943; Vector Backbone:pMT-GW; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:29 | 0 | |
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pQUAST-shibire (ts1) Resource Report Resource Website |
RRID:Addgene_24362 | Shibire (ts1) | Drosophila melanogaster | Ampicillin | PMID:20434990 | Shibire was PCR amplified from genomic DNA of UAS-shibire transgenic flies (Kitamoto, 2001) using genUASFOR and genUASREVsv40 oligos, and ligated into the NotI/KpnI sites of pQUAST. | Backbone Size:9000; Vector Backbone:pQUAST; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:31 | 0 | |
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pQUAST>stop>shibire (ts1) Resource Report Resource Website |
RRID:Addgene_24363 | Shibire (ts1) | Drosophila melanogaster | Ampicillin | PMID:20434990 | The NotI fragment containing the mCD8-GFP cassette was excised from pQUAS>stop>mCD8- GFP, the vector was blunted, and ligated to a blunted NotI/KpnI shibirets1 isolated from pQUAST-shibirets1. ts1 | Backbone Size:9000; Vector Backbone:pQUAS>stop>mCD8-GFP; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:30 | 0 | |
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pAc5.1B-EGFP-DmHPat Resource Report Resource Website |
RRID:Addgene_25029 | HPat | Drosophila melanogaster | Ampicillin | PMID:20404111 | Backbone Marker:Elisa Izaurralde; Backbone Size:6080; Vector Backbone:pAc5.1B-EGFP; Vector Types:Drosophila expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:12:36 | 0 |
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