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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
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pUC19-K2FTY8 Resource Report Resource Website |
RRID:Addgene_103079 | K2FTY8(Cas9 coding gene from Alcanivorax pacificus W11-5) | Other | Ampicillin | PMID:29529247 | Backbone Marker:NEB(New England Biolabs); Vector Backbone:pUC19; Vector Types:CRISPR, Cloning vector; Bacterial Resistance:Ampicillin | human codon-optimized | 2026-07-25 12:33:53 | 0 | |
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pUC19-D3NT09 Resource Report Resource Website |
RRID:Addgene_103074 | D3NT09(Cas9 coding gene from Azospirillum sp. (strain B510)) | Other | Ampicillin | PMID:29529247 | Backbone Marker:NEB(New England Biolabs); Vector Backbone:pUC19; Vector Types:CRISPR, Cloning vector; Bacterial Resistance:Ampicillin | human codon-optimized | 2026-07-25 12:33:53 | 0 | |
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pUC19-E6KTN8 Resource Report Resource Website |
RRID:Addgene_103076 | E6KTN8(Cas9 coding gene from Actinomyces sp. oral taxon 180 str. F0310) | Other | Ampicillin | PMID:29529247 | Backbone Marker:NEB(New England Biolabs); Vector Backbone:pUC19; Vector Types:CRISPR, Cloning vector; Bacterial Resistance:Ampicillin | human codon-optimized | 2026-07-25 12:33:53 | 0 | |
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pUC19-E3CY56 Resource Report Resource Website |
RRID:Addgene_103075 | E3CY56(Cas9 coding gene from Aminomonas paucivorans DSM 12260) | Other | Ampicillin | PMID:29529247 | Backbone Marker:NEB(New England Biolabs); Vector Backbone:pUC19; Vector Types:CRISPR, Cloning vector; Bacterial Resistance:Ampicillin | human codon-optimized | 2026-07-25 12:33:53 | 0 | |
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PresentER-SIINFEKL (mCherry) Resource Report Resource Website 1+ mentions |
RRID:Addgene_102945 | SIINFEKL | Gallus gallus | Ampicillin | PMID:30499773 | Please visit https://www.biorxiv.org/content/early/2018/09/22/267047 for bioRxiv preprint. | Backbone Size:8200; Vector Backbone:PresentER; Vector Types:Mammalian Expression, Retroviral; Bacterial Resistance:Ampicillin | OVA257-264 | 2026-07-25 12:33:52 | 4 |
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pHMR1A Resource Report Resource Website |
RRID:Addgene_102957 | MR1A cDNA | Homo sapiens | Ampicillin | PMID:24832684 | Backbone Marker:Invitrogen; Backbone Size:3908; Vector Backbone:pCR2.1-TOPO; Vector Types:Cloning; Bacterial Resistance:Ampicillin | Stop codon has been removed by HindIII site | 2026-07-25 12:33:52 | 0 | |
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pET22b_PfSSB_W166C Resource Report Resource Website |
RRID:Addgene_103001 | PfSSB_W166C | Plasmodium falciparum | Ampicillin | PMID:29466468 | Usage: The expressed protein is a Plasmodium falciparum single-stranded DNA-binding protein, PfSSB, with two point mutations, C93A and W166C, for subsequent labeling at the 166 cysteine with one IDCC (N-[2-(iodoacetamido)ethyl]-7-diethylaminocoumarin-3-carboxamide) or Cy3B per subunit. PfSSB was expressed without the N-terminal apicoplast localisation sequence (76 amino acids) but amino acids are numbered for the full-length protein, that is the first amino acid in the expressed protein is M77.W166C is the equivalent position to W88 in E. coli SSB, which was labeled with Cy3B for single molecule measurements of DNA unwinding using TIRF (Fili, N.; Mashanov, G.; Toseland, C. P.; Batters, C.; Wallace, M. I.; Yeeles, J. T. P.; Dillingham, M. S.; Webb, M. R.; Molloy, J. E., Visualizing DNA unwinding by helicases at the single molecule level. Nucleic Acids Res. 2010, 38, 4448-4457.) Protocol: See Hedgethorne and Webb (2012), which is also followed for PfSSB purification, except with the omission of the PEI precipitation step. Hedgethorne, K.; Webb, M. R., Fluorescent SSB as a reagentless biosensor for single-stranded DNA. Methods Mol. Biol. 2012, 922, 219-233. | Vector Backbone:pET22B; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | C93A, W166C | 2026-07-25 12:33:53 | 0 |
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pET22b_PfSSB Resource Report Resource Website 1+ mentions |
RRID:Addgene_103000 | PfSSB | Plasmodium falciparum | Ampicillin | PMID:29466468 | The expressed protein is a Plasmodium falciparum single-stranded DNA-binding protein, PfSSB, for subsequent labeling at the single, native cysteine with one IDCC (N-[2-(iodoacetamido)ethyl]-7-diethylaminocoumarin-3-carboxamide) per subunit. This adduct is then used as a fluorescent single-stranded DNA (ssDNA) biosensor, having ~20-fold fluorescence increase on binding ssDNA with very high affinity. PfSSB was expressed without the N-terminal apicoplast localisation sequence (76 amino acids) but amino acids are numbered for the full-length protein, that is the first amino acid in the expressed protein is M77. Protocol See Hedgethorne and Webb (2012), which is also followed for PfSSB purification, except with the omission of the PEI precipitation step. Hedgethorne, K.; Webb, M. R., Fluorescent SSB as a reagentless biosensor for single-stranded DNA. Methods Mol. Biol. 2012, 922, 219-233. | Vector Backbone:pET22B; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 1 | |
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pUCmini-iCAP-PHP.B2 Resource Report Resource Website |
RRID:Addgene_103003 | Synthetic construct isolate AAV-PHP.B2 VP1 gene | Synthetic | Ampicillin | PMID:26829320 | Please note that this is a non-standard rep-cap construct. It uses a tTA-TRE amplification loop to increase Capsid expression and AAV production. We find that this system increases AAV titers 1.5-5 fold (Ben Deverman, Bryan Simpson and Paul Patterson, unpublished data). This is a tet-off system, so no dox or tet is needed to turn it on. It can be used like any other rep-cap plasmid. *This system should only present a problem if the rAAV genome to be packaged has a tet responsive element that directs expression of a protein that affected the health of the production cells. The introduction of an XbaI restriction site for ease of cloning introduces a K449R mutation, which does not have an overt effect on vector production or transduction. | Vector Backbone:pUC57-mini; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 0 | |
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pUCmini-iCAP-PHP.B Resource Report Resource Website 10+ mentions |
RRID:Addgene_103002 | Synthetic construct isolate AAV-PHP.B VP1 gene | Synthetic | Ampicillin | PMID:26829320 | Please note that this is a non-standard rep-cap construct. It uses a tTA-TRE amplification loop to increase Capsid expression and AAV production. We find that this system increases AAV titers 1.5-5 fold (Ben Deverman, Bryan Simpson and Paul Patterson, unpublished data). This is a tet-off system, so no dox or tet is needed to turn it on. It can be used like any other rep-cap plasmid. *This system should only present a problem if the rAAV genome to be packaged has a tet responsive element that directs expression of a protein that affected the health of the production cells. The introduction of an XbaI restriction site for ease of cloning introduces a K449R mutation, which does not have an overt effect on vector production or transduction. | Vector Backbone:pUC57-mini; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 12 | |
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pUCmini-iCAP-PHP.eB Resource Report Resource Website 100+ mentions |
RRID:Addgene_103005 | Synthetic construct isolate AAV-PHP.eB VP1 gene | Synthetic | Ampicillin | PMID:28671695 | Please note that this is a non-standard rep-cap construct. It uses a tTA-TRE amplification loop to increase Capsid expression and AAV production. We find that this system increases AAV titers 1.5-5 fold (Ben Deverman, Bryan Simpson and Paul Patterson, unpublished data). This is a tet-off system, so no dox or tet is needed to turn it on. It can be used like any other rep-cap plasmid. This system should only present a problem if the rAAV genome to be packaged has a tet responsive element that directs expression of a protein that affected the health of the production cells. The introduction of an XbaI restriction site for ease of cloning introduces a K449R mutation, which does not have an overt effect on vector production or transduction. | Vector Backbone:pUC57-mini; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 121 | |
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pUCmini-iCAP-PHP.B3 Resource Report Resource Website |
RRID:Addgene_103004 | Synthetic construct isolate AAV-PHP.B3 VP1 gene | Synthetic | Ampicillin | PMID:26829320 | Please note that this is a non-standard rep-cap construct. It uses a tTA-TRE amplification loop to increase Capsid expression and AAV production. We find that this system increases AAV titers 1.5-5 fold (Ben Deverman, Bryan Simpson and Paul Patterson, unpublished data). This is a tet-off system, so no dox or tet is needed to turn it on. It can be used like any other rep-cap plasmid. *This system should only present a problem if the rAAV genome to be packaged has a tet responsive element that directs expression of a protein that affected the health of the production cells. The introduction of an XbaI restriction site for ease of cloning introduces a K449R mutation, which does not have an overt effect on vector production or transduction. | Vector Backbone:pUC57-mini; Vector Types:Mammalian Expression, AAV; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 0 | |
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pJH124 Resource Report Resource Website |
RRID:Addgene_102951 | APEX2-NES | Saccharomyces cerevisiae | Ampicillin | PMID:27274088 | Backbone Marker:ATCC; Backbone Size:7500; Vector Backbone:pRS425; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:52 | 0 | ||
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pZL1-ZF - myelin basic protein a (mbpa) Resource Report Resource Website |
RRID:Addgene_103007 | myelin basic protein | Danio rerio | Ampicillin | PMID:12112375 | Backbone Size:4308; Vector Backbone:pZL1; Vector Types:; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 0 | ||
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GESTALT_pX330-v1 Resource Report Resource Website |
RRID:Addgene_103061 | integration of Cas9 with guide targeting GESTALT barcodes V1 to V5 | Homo sapiens | Ampicillin | PMID:27229144 | Derived from pX330-U6-Chimeric_BB-CBh-hSpCas9 | Vector Backbone:lentiCRISPR v2 (#52961); Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 0 | |
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pCAGGS_3E5E_luciferase Resource Report Resource Website 1+ mentions |
RRID:Addgene_103055 | Ebolavirus minigenome | Zaire ebolavirus, Mayinga variant | Ampicillin | PMID:28807685 | Vector Backbone:pCAGGs; Vector Types:Mammalian Expression, Luciferase; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 2 | ||
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pCAGGS_L_EBOV Resource Report Resource Website 1+ mentions |
RRID:Addgene_103052 | L gene of Ebola virus | Zaire ebolavirus, Mayinga | Ampicillin | PMID:28807685 | Vector Backbone:pCAGGs; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 4 | ||
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pCAGGS_VP30_EBOV Resource Report Resource Website 1+ mentions |
RRID:Addgene_103051 | VP30 gene of Ebola virus | Zaire ebolavirus, Mayinga | Ampicillin | PMID:28807685 | Vector Backbone:pCAGGs; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 3 | ||
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pCAGGS_HA-VP35_EBOV Resource Report Resource Website 1+ mentions |
RRID:Addgene_103053 | VP35 | Zaire ebolavirus, Mayinga | Ampicillin | PMID:27252530 | Vector Backbone:pCAGGs; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 1 | ||
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pNB22 Resource Report Resource Website |
RRID:Addgene_103059 | GFP-OVA | Other | Ampicillin | PMID:24439899 | A short ovalbumin epitope (amino acids 319–343) was fused to GFP (pGFP_OVA) to follow the immune response to the expressed antigen. (Bumann, 2001). | Vector Backbone:pBR322; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-07-25 12:33:53 | 0 |
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