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Plasmid Name Proper Citation Insert Name Organism Bacterial Resistance Defining Citation Comments Vector Backbone Description Relevant Mutation Record Last Update Mentions Count
pSico_U6-PGC1a1 sgRNA
 
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RRID:Addgene_165425 gRNA against PGC-1a variant 1 Homo sapiens Ampicillin PMID:33626346 Backbone Size:9580; Vector Backbone:pSico; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin 2026-08-29 12:59:23 0
pBI-p73 wt/EGFP
 
Resource Report
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1+ mentions
RRID:Addgene_16545 p73 Homo sapiens Ampicillin PMID:10588737 Tet-responsive p73 expression construct. Backbone Size:5210; Vector Backbone:pBI-MCS-EGFP; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-29 12:59:24 1
pBI-MCS-EGFP
 
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1+ mentions
RRID:Addgene_16542 Ampicillin PMID:10588737 The tet-responsive reporter plasmid pBI-EGFP was purchased from Clontech and modified by the inclusion of a polylinker to create pBI-MCS-EGFP. Backbone Size:5210; Vector Backbone:pBI-MCS-EGFP; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-29 12:59:23 9
tTA-IRES-Neo
 
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1+ mentions
RRID:Addgene_16541 tTA Ampicillin PMID:10588737 tTA is a a tetracycline-controlled transactivator generated by fusing the tet repressor with the activating domain of virion protein 16 of herpes simplex virus. tTA-IRES-Neo was generated by cloning PCR-amplified tTA cDNA from pUHD15-1 (Gossen, M. & Bujard, H., 1992, PNAS 89, 5547-5551) into the XbaI site of plasmid pMk10-59 (Kobayashi, M et al., 1996, Biotechniques 21, 398-402). Backbone Size:6000; Vector Backbone:pMk10-59; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-29 12:59:25 1
MSCV-Tox2-IRES-eGFP
 
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RRID:Addgene_165428 TOX2 Mus musculus Ampicillin PMID:31152140 Backbone Marker:Tannishtha Reya Lab; Backbone Size:6400; Vector Backbone:MSCV-IRES-eGFP; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-29 12:59:23 0
pSico_U6-Pan-PGC1a sgRNA
 
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RRID:Addgene_165426 gRNA against human Total PGC-1a variants Homo sapiens Ampicillin PMID:33626346 Backbone Size:9580; Vector Backbone:pSico; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin 2026-08-29 12:59:26 0
pAAV-syn-SnFR-gamma8-minWPRE
 
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RRID:Addgene_165498 iGluSnFR extracellular domain fused to TARP gamma-8 via NETO2 TM domain Rattus norvegicus Ampicillin PMID:36622100 Chimera of iGluSnFR (Addgene plasmid # 41732), Neto2 and Gamma-8 pAAV backbone is based on Addgene plasmid # 61463 Please visit https://doi.org/10.1101/2021.01.21.427382 for bioRxiv preprint. Backbone Size:3950; Vector Backbone:pAAV; Vector Types:AAV; Bacterial Resistance:Ampicillin 2026-08-29 12:59:24 0
pMMB206-CT81
 
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RRID:Addgene_165411 CT81 gene circuit Synthetic Chloramphenicol PMID:33558556 pMMB206 backbone is very low copy, <10 copies. Backbone Size:9311; Vector Backbone:pMMB206; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol 2026-08-29 12:59:23 0
pGEM-HE-Glyco-Venus-bPAC(S27A)
 
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RRID:Addgene_165490 Glyco-Venus-bPAC(S27A)-Myc Synthetic Ampicillin PMID:34663304 Backbone Size:3009; Vector Backbone:pGEM HE; Vector Types:Bacterial Expression, cDNA expression, Xenopus Oocyte; Bacterial Resistance:Ampicillin 2026-08-29 12:59:24 0
pGST-PPARalpha
 
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RRID:Addgene_16550 PPAR alpha Homo sapiens Ampicillin PMID:10555149 Backbone Marker:Amersham; Backbone Size:5000; Vector Backbone:pGEX-2TK; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin N-terminal DNA-binding domain: aa 1-249 2026-08-29 12:59:27 0
pSIN-TRE-H2BeGFP-rtTA2
 
Resource Report
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1+ mentions
RRID:Addgene_165494 Human histone H2B Homo sapiens Ampicillin PMID:29944140 ABOUT BACKBONE: The lentiviral backbone was originally designed and constructed by Barde I et al. (Barde I et al. Mol Ther. 2006. 13(2): 382-90. PMID: 16275162). ABOUT TEST DIGESTION: Since Xba I restriction site is lost during cloning, we recommend checking the plasmid using the enzymes: Xho I and Nhe I. You should get two fragments around 1600 bp (insert+vector) and 7500 bp (vector). Backbone Marker:-; Backbone Size:8023; Vector Backbone:pRRL-cPPT-hPGKTMPrtTA-WPRE; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin - 2026-08-29 12:59:27 1
pAAV Syn 2xLyn-ERex-Venus-bPAC(F198Y)
 
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RRID:Addgene_165491 2xLyn-ERex-Venus-bPAC(F198Y) Synthetic Ampicillin PMID:34663304 Backbone Marker:Stratagene; Backbone Size:4697; Vector Backbone:pAAV; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin 2026-08-29 12:59:27 0
pAAV-Syn-2xLyn-ERex-Venus(Y145W)-bPAC(F198Y)
 
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RRID:Addgene_165492 2xLyn-ERex-Venus(Y145W)-bPAC(F198Y) Synthetic Ampicillin PMID:34663304 This plasmid is identical to PACmn but with a point mutation in Venus to reduce fluorescence by about 90% to facilitate combining with fluorescent indicators etc. It was not used in the original publication. Backbone Marker:Stratagene; Backbone Size:4697; Vector Backbone:pAAV; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin 2026-08-29 12:59:24 0
pRha-ABE8e-NRCH
 
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RRID:Addgene_165417 ABE8e-NRCH Synthetic Kanamycin Backbone Marker:Atum; Backbone Size:2253; Vector Backbone:pD881-SR; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin 2026-08-29 12:59:23 0
pBXPHM3-PCFT_NB
 
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RRID:Addgene_165415 GgPCFT_NB Gallus gallus Ampicillin PMID:34040256 Backbone Size:6994; Vector Backbone:pBXNPHM3; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-29 12:59:26 0
pOpen-Pwopol
 
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RRID:Addgene_165562 Pwo DNA Polymerase Other Ampicillin DNA polymerase; additionally exhibits 3' to 5' exonuclease activity. The plasmids in the Open Enzyme collection contain genetic parts and are not functional by themselves. Researchers can clone these enzymes into an expression vector of their choice and then transform into E. coli bacteria for expression and purification. Additional information can be found at https://www.addgene.org/depositor-collections/open-enzyme/. Vector Backbone:pBuild; Vector Types:Synthetic Biology; Bacterial Resistance:Ampicillin 2026-08-29 12:59:25 0
pOpen-XbaIR
 
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RRID:Addgene_165567 XbaI Other Ampicillin Type II restriction enzyme that recognizes the double-stranded sequence TCTAGA and cleaves after T-1. The plasmids in the Open Enzyme collection contain genetic parts and are not functional by themselves. Researchers can clone these enzymes into an expression vector of their choice and then transform into E. coli bacteria for expression and purification. Additional information can be found at https://www.addgene.org/depositor-collections/open-enzyme/. Vector Backbone:pBuild; Vector Types:Synthetic Biology; Bacterial Resistance:Ampicillin 2026-08-29 12:59:25 0
pOpen-NcoIR
 
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RRID:Addgene_165568 NcoI Other Ampicillin Type II restriction enzyme that recognizes the double-stranded sequence CCATGG and cleaves after C-1. The plasmids in the Open Enzyme collection contain genetic parts and are not functional by themselves. Researchers can clone these enzymes into an expression vector of their choice and then transform into E. coli bacteria for expression and purification. Additional information can be found at https://www.addgene.org/depositor-collections/open-enzyme/. Vector Backbone:pBuild; Vector Types:Synthetic Biology; Bacterial Resistance:Ampicillin 2026-08-29 12:59:25 0
dCas9-MSK1
 
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RRID:Addgene_165601 ribosomal protein S6 kinase A5 Homo sapiens Ampicillin PMID:33563994 Vector Backbone:LentiCRISPR v2; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin 2026-08-29 12:59:25 0
pOpen-RNAse A
 
Resource Report
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RRID:Addgene_165565 RNAse A Other Ampicillin Ribonuclease A or RNase A; endoribonuclease purified from bovine pancreas. Important enzyme for the removal of RNA for RNA free DNA purification reactions such as plasmid DNA purification and genomic DNA purification, RNA removal from recombinant protein preparations, ribonuclease protection assays, mapping single-base mutations in DNA/RNA. Effectively cleaves the phosphodiester bond between the 5'-ribose of a nucleotide and the phosphate group attached to the 3'-ribose of an adjacent pyrimidine nucleotide which forms a 2',3'-cyclic phosphate which is then hydrolyzed to the corresponding 3'-nucleoside phosphate. The plasmids in the Open Enzyme collection contain genetic parts and are not functional by themselves. Researchers can clone these enzymes into an expression vector of their choice and then transform into E. coli bacteria for expression and purification. Additional information can be found at https://www.addgene.org/depositor-collections/open-enzyme/. Vector Backbone:pBuild; Vector Types:Synthetic Biology; Bacterial Resistance:Ampicillin 2026-08-29 12:59:25 0

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