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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
Comments |
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|---|---|---|---|---|---|---|---|---|---|---|
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pYPQ134B2.0 Resource Report Resource Website |
RRID:Addgene_167158 | Tetracycline | PMID:34168320 | Backbone Marker:Cermak et al. 2011; Vector Backbone:pHD1; Vector Types:Plant Expression, CRISPR; Bacterial Resistance:Tetracycline | 2026-08-15 01:09:41 | 0 | ||||
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∆DUSP6 Resource Report Resource Website 1+ mentions |
RRID:Addgene_27977 | DUSP6 | Homo sapiens | Tetracycline | PMID:23839489 | Catalytically inactive DUSP6 | Backbone Marker:Thermo Scientific; Backbone Size:11000; Vector Backbone:pLEX-HA-MYC; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Tetracycline | C293S: mutation in the phosphatase domain | 2026-08-15 01:13:09 | 1 |
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DUSP6 Resource Report Resource Website 1+ mentions |
RRID:Addgene_27975 | DUSP6 | Homo sapiens | Tetracycline | PMID:23839489 | Backbone Marker:Thermo Scientific; Backbone Size:11000; Vector Backbone:pLEX-MCS; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Tetracycline | 2026-08-15 01:13:09 | 4 | ||
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pLEX SC4MOL 519 Resource Report Resource Website |
RRID:Addgene_27984 | SC4MOL | Homo sapiens | Tetracycline | H173Q caused by 519T->A mutation as described in He et al., J Clin Invest. 2011;121(3):976–984. PMID: 21285510 | Backbone Size:11000; Vector Backbone:pLEX; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Tetracycline | H173Q mutation in SC4MOL | 2026-08-15 01:13:08 | 0 | |
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pLEX SC4MOL Resource Report Resource Website |
RRID:Addgene_27983 | SC4MOL | Homo sapiens | Tetracycline | Backbone Size:11000; Vector Backbone:pLEX; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Tetracycline | 2026-08-15 01:13:09 | 0 | |||
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pTGV-Express-Tet SMR5918 Resource Report Resource Website |
RRID:Addgene_28035 | Tetracycline | PMID:11483365 | Note that Addgene's sequencing results found a 1 nucleotide deletion at bp# 4286 when compared with the sequence provided by the depositing laboratory. This deletion is not known to affect plasmid function. | Backbone Size:8493; Vector Backbone:n/a; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:13:10 | 0 | |||
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pNH10 Resource Report Resource Website |
RRID:Addgene_40861 | repeat NH10 | Xanthomonas oryzae | Tetracycline | PMID:21493687 | Backbone Size:3013; Vector Backbone:pTC14; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:39 | 0 | ||
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pNH6 Resource Report Resource Website |
RRID:Addgene_40857 | repeat NH6 | Xanthomonas oryzae | Tetracycline | PMID:21493687 | Backbone Size:3013; Vector Backbone:pTC14; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:39 | 0 | ||
|
pNH4 Resource Report Resource Website |
RRID:Addgene_40855 | repeat NH4 | Xanthomonas oryzae | Tetracycline | PMID:21493687 | Backbone Size:3013; Vector Backbone:pTC14; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:39 | 0 | ||
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pNH2 Resource Report Resource Website |
RRID:Addgene_40853 | repeat NH2 | Xanthomonas oryzae | Tetracycline | PMID:21493687 | Backbone Size:3013; Vector Backbone:pTC14; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:39 | 0 | ||
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pNH8 Resource Report Resource Website |
RRID:Addgene_40859 | repeat NH8 | Xanthomonas oryzae | Tetracycline | PMID:21493687 | Backbone Size:3013; Vector Backbone:pTC14; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:39 | 0 | ||
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pPROBE-TT Resource Report Resource Website 1+ mentions |
RRID:Addgene_37822 | Promotorless gfp reporter gene | bacteria | Tetracycline | PMID:11059491 | Please refer to the attached table for a complete list of restriction sites in the MCS. This plasmid has the PstI site. | Vector Backbone:pBBR1; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:17 | 1 | |
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pPROBE-TT' Resource Report Resource Website |
RRID:Addgene_37823 | Promotorless gfp reporter gene | bacteria | Tetracycline | PMID:11059491 | Please refer to the attached table for a complete list of restriction sites in the MCS. This plasmid has the PstI site. | Vector Backbone:pBBR1; Vector Types:; Bacterial Resistance:Tetracycline | 2026-08-15 01:14:17 | 0 | |
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pCM157 Resource Report Resource Website 1+ mentions |
RRID:Addgene_45863 | cre recombinase | Enterobacteria phage P1 | Tetracycline | PMID:12449384 | The 1.1-kb XbaI-EcoRI fragment from pJW168 (PMID 9858684) was cloned between the XbaI and EcoRI sites of pCM62 (Addgene plasmid 45826) to generate the tetracycline-resistance conferring cre expression plasmid. Used with allelic exhange vectors--Addgene plasmids 46012 or 46013--to generate unmarked mutant strains in a broad bacterial host range. | Backbone Marker:Lidstrom Lab (Addgene plasmid 45826); Backbone Size:6878; Vector Backbone:pCM62; Vector Types:Bacterial Expression, Cre/Lox; Bacterial Resistance:Tetracycline | 2026-08-15 01:15:27 | 2 | |
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pCM130 Resource Report Resource Website 1+ mentions |
RRID:Addgene_45828 | Tetracycline | PMID:11495985 | XylE replaces the lac promoter in pCM62 (Addgene plasmid 45826) and is used as a reporter to test promoter activity. A transcriptional terminator was added to reduce background activity. | Backbone Marker:Lidstrom Lab (Addgene plasmid 45826); Backbone Size:7965; Vector Backbone:pCM62; Vector Types:low-background broad-host-range promoter-probe vector using xylE as a reporter gene; Bacterial Resistance:Tetracycline | 2026-08-15 01:15:26 | 3 | |||
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pOSIP-TT (TetR, P21) Resource Report Resource Website |
RRID:Addgene_45989 | Tetracycline | PMID:24050148 | Reference: St-Pierre F, Cui L et al., "One-step cloning and chromosomal integration of DNA", ACS Synthetic Biology, http://pubs.acs.org/doi/abs/10.1021/sb400021j | Backbone Size:7395; Vector Backbone:pOSIP; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:15:28 | 0 | |||
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pKNOCK-Tc Resource Report Resource Website 1+ mentions |
RRID:Addgene_46259 | Tetracycline | PMID:10337469 | Vector Backbone:original; Vector Types:Bacterial targeting; Bacterial Resistance:Tetracycline | 2026-08-15 01:15:30 | 2 | ||||
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pINIT_tet Resource Report Resource Website |
RRID:Addgene_46974 | Tetracycline | PMID:21410291 | Backbone Marker:unknown; Backbone Size:5595; Vector Backbone:pBR322; Vector Types:sequencing vector; Bacterial Resistance:Tetracycline | 2026-08-15 01:15:37 | 0 | ||||
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pDMS197 Resource Report Resource Website |
RRID:Addgene_43831 | Tetracycline | PMID:9511756 | The plasmids deposited here comprise a set of SacB1-dependent allelic exchange vectors improved from a previously described suicide vector, pGP704 (Miller and Mekalanos, 1988), by including a system to select for plasmid loss by recombination. Plasmid pRE107 (Addgene plasmid #43829) was constructed by cloning the appropriate EcoRI fragment from pUC58-sacB1 (McIver et al., 1995) into pGP704 (see associated schematic image). The sacB1 allele is a modified variation of sacB, where unique restriction sites were removed by site directed mutagenesis (McIver et al., 1995). Additionally, the BamHI site in the R6K ori of the resulting plasmid was removed by partial BamHI digestion, blunting the resulting overhangs with PolIk (resulting in the formation of a ClaI site) and screening for its loss by restriction analysis. To use this plasmid with bla fusions and increase the functionality of this system, the depositing laboratory replaced the ApR gene as follows. The ApR gene flanked by the remaining BamHI sites was removed and replaced with either CmR, TcR or KmR resistance markers (see associated schematic image). The TcR gene was cloned on a blunted EcoRI–StyI fragment from pBR322 into the blunted BamHI sites to give pDMS197. The BamHI site near the MCS was regenerated after cloning; the BamHI site near the 5' end of TcR/TetR was not. The resulting plasmid together with others in this deposited series contain the conditional R6K ori, the origin of transfer (oriT) which allows conjugative transfer from permissive hosts, the sacB1 gene to provide negative selection and a MCS, along with a range of different AbR markers. Moreover, the use of Tc also allows an alternative negative selection using fusaric acid and chlortetracycline as described previously (Maloy and Nunn, 1981). | Backbone Marker:Addgene plasmid 43829; Backbone Size:5173; Vector Backbone:pRE107 (modified from pGP704); Vector Types:Bacterial Expression, Bacterial allelic exchange vector with sacB1; Bacterial Resistance:Tetracycline | 2026-08-15 01:15:10 | 0 | |||
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pMflET-o4 Resource Report Resource Website 1+ mentions |
RRID:Addgene_101314 | oriC4 of M. florum strain L1 (rpmH/dnaA and dnaA/dnaN intergenic regions, with dnaA) | Mesoplasma florum | Tetracycline | PMID:28115382 | Vector Backbone:colE1; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:00:19 | 1 |
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