Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
Comments |
||||
|---|---|---|---|---|---|---|---|---|---|---|
|
pOS1T-chPylRS4OxzA Resource Report Resource Website |
RRID:Addgene_253663 | chPylRS-4OxzA | Synthetic | Tetracycline | PMID:41885601 | Please visit https://doi.org/10.1101/2025.11.04.686677 for bioRxiv preprint. | Backbone Marker:in-house design and optimization; Vector Backbone:pOS1T; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:36:09 | 0 | |
|
pOS1T-Mb(IPYE)PylRSτMH Resource Report Resource Website |
RRID:Addgene_253665 | Mb(IPYE)PylRS-τMH | Tetracycline | PMID:41885601 | Please visit https://doi.org/10.1101/2025.11.04.686677 for bioRxiv preprint. | Backbone Marker:in-house design and optimization; Vector Backbone:pOS1T; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:36:07 | 0 | ||
|
pOS1T-MmPylRS(8_2) Resource Report Resource Website |
RRID:Addgene_253670 | MmPylRS(8_2) | Synthetic | Tetracycline | PMID:41885601 | Please visit https://doi.org/10.1101/2025.11.04.686677 for bioRxiv preprint. | Backbone Marker:in-house design and optimization; Vector Backbone:pOS1T; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:36:09 | 0 | |
|
pOS1T-chPylR2E5MH Resource Report Resource Website |
RRID:Addgene_253657 | chPylRS-2E5MH | Synthetic | Tetracycline | PMID:41885601 | Please visit https://doi.org/10.1101/2025.11.04.686677 for bioRxiv preprint. | Backbone Marker:in-house design and optimization; Vector Backbone:pOS1T; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:36:09 | 0 | |
|
US0 pyrF-/hisB-/tnaA- Resource Report Resource Website |
RRID:Addgene_228512 | pyrF-/hisB-/tnaA- | n/a | Tetracycline | PMID:39610115 | Derived from US0 pyrF-/hisB- (Scot Wolfe, Addgene #12614). This strain has a deletion in both the hisB and pyrF genes (the bacterial homologs of HIS3 and URA3) and it contains a F' episome bearing the lacl^q repressor. This strain is also has a deletion in tnaA gene and does not produce indole, verified by Kovac's Reagent. Please visit https://doi.org/10.1101/2024.08.07.607023 for bioRxiv preprint. | Vector Backbone:n/a; Vector Types:This is a strain, not a plasmid; Bacterial Resistance:Tetracycline | 2026-08-15 01:31:50 | 0 | |
|
pNDGG004 Resource Report Resource Website |
RRID:Addgene_231317 | Tetracycline | PMID:39919271 | Vector Backbone:NA; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:32:04 | 0 | ||||
|
pCnRed Resource Report Resource Website |
RRID:Addgene_232908 | gam | Synthetic | Tetracycline | PMID:39989320 | Vector Backbone:pSa; Vector Types:Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:33:07 | 0 | ||
|
pNDMS237 Resource Report Resource Website |
RRID:Addgene_248095 | sfYFP | Tetracycline | Backbone Marker:Barney Geddes; Vector Backbone:pNDGG004 (Addgene #231317); Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:34:43 | 0 | ||||
|
pNDMS239 Resource Report Resource Website |
RRID:Addgene_248096 | mScarlet-I | Tetracycline | Backbone Marker:Barney Geddes; Vector Backbone:pNDGG004 (Addgene #231317); Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:34:44 | 0 | ||||
|
pJS1 Resource Report Resource Website |
RRID:Addgene_253726 | dcas9 | Streptococcus pasteurianus | Tetracycline | PMID:41670347 | Vector Backbone:miniCTX1; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:35:31 | 0 | ||
|
pMVV207 Resource Report Resource Website |
RRID:Addgene_215343 | S. stutzeri nifL gRNA | Synthetic | Tetracycline | PMID:37988619 | Vector Backbone:RSF1010; Vector Types:Bacterial Expression, CRISPR, Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:29:51 | 0 | ||
|
pSW003-PpsbA-mNeonGreen Resource Report Resource Website |
RRID:Addgene_205019 | mNeonGreen | Synthetic | Tetracycline | PMID:29449848 | Backbone Marker:Dieter Haas; obtained from Culture Collection of Switzerland; Vector Backbone:pME6031 (Several restriction sites were removed to facilitate cloning); Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | mNeonGreen is codon optimized for expression in P. fluorescens | 2026-08-15 01:27:45 | 0 | |
|
pSW002-PpsbA-mNeonGreen Resource Report Resource Website |
RRID:Addgene_205017 | mNeonGreen | Synthetic | Tetracycline | PMID:29449848 | Backbone Marker:Dieter Haas; obtained from Culture Collection of Switzerland; Vector Backbone:pME6031 (Several restriction sites were removed to facilitate cloning); Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | mNeonGreen is codon optimized for expression in P. fluorescens | 2026-08-15 01:27:48 | 0 | |
|
pMflT-o4-mNG Resource Report Resource Website 1+ mentions |
RRID:Addgene_201855 | mNeonGreen | Synthetic | Tetracycline | The user should always streak the culture on plate and work with isolated fluorescent colonies. Addgene NGS results found mixed population of nucleotides across Term_apFAB390 and C-terminus of NeonGreen, but plasmid function should not be affected. | Vector Backbone:pMflT-o4; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:27:52 | 1 | ||
|
pJLG039 Resource Report Resource Website |
RRID:Addgene_192982 | T7 polymerase | E. coli | Tetracycline | PMID:36645284 | The T7 polymerase gene (1) was cloned from the chromosome of BL21(DE3). | Backbone Size:8751; Vector Backbone:pSW213; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:26:34 | 0 | |
|
pMflT-o4-YFP Resource Report Resource Website |
RRID:Addgene_201856 | LanYFP | Synthetic | Tetracycline | Vector Backbone:pMflT-o4; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:26:45 | 0 | |||
|
pALS3-Ma-sfGFP-WT Resource Report Resource Website |
RRID:Addgene_212119 | SUMO-sfGFP-WT | Tetracycline | This plasmid encodes expression of a) sfGFP-WT, uninterrupted by TAG codons, and b) Methanomethylophilus alvus tRNA(6). It is to be paired with a plasmid that expresses M. alvus pyrrolysyl-tRNA synthetase (MaRS). This control plasmid is used during fluorescence-based selection and characterization of one or more MaRS mutants. It is distinguished from a previous Ma version by containing a tetracycline efflux marker. | Backbone Size:4807; Vector Backbone:pALS3; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:30:28 | 0 | |||
|
pALS3-Ma-SUMO-sfGFP-WT Resource Report Resource Website |
RRID:Addgene_212122 | SUMO-sfGFP-WT | Tetracycline | This plasmid encodes expression of a) sumo-sfGFP, uninterrupted by TAG codons, and b) Methanomethylophilus alvus pyrrolysine tRNA(6). It is to be paired with a plasmid that expresses M. alvus pyrrolysyl-tRNA synthetase (MaRS). This pALS3 control plasmid is used during fluorescence-based selection and characterization of Ma RS mutants. The plasmid here is distinguished from a previous Ma version by the presence of a tetracycline efflux marker. | Backbone Size:4807; Vector Backbone:pALS3; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | 2026-08-15 01:30:28 | 0 | |||
|
pALS3-Ma-SUMO-TAG35-sfGFP Resource Report Resource Website |
RRID:Addgene_212120 | SUMO-TAG35-sfGFP | Tetracycline | This plasmid encodes expression of a) SUMO-sfGFP with an amber (TAG) codon at E35 within the SUMO coding region and b) Methanomethylophilus alvus tRNA(6). It is to be paired with a plasmid that expresses an M. alvus pyrrolysyl-tRNA synthetase (MaRS). This plasmid is used during fluorescence-based selection and characterization of one or more MaRS mutants. It is distinguished from the previous Ma version by containing a tetracycline efflux marker. The SUMO linker is included in order to distance the TAG site from sfGFP. | Backbone Size:4807; Vector Backbone:pALS3; Vector Types:Bacterial Expression; Bacterial Resistance:Tetracycline | E35TAG (within SUMO encoding sequence) | 2026-08-15 01:30:28 | 0 | ||
|
pHBJT010 Resource Report Resource Website |
RRID:Addgene_225161 | Tetracycline | PMID:39244484 | Low copy plasmid (pSC101 ori and repA), pUC18 MCS with FLAG epitope integrated at SmaI site, confers tetracycline resistance | Backbone Size:4297; Vector Backbone:Unknown; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Tetracycline | 2026-08-15 01:30:32 | 0 |
Can't find your Plasmid?
We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific plasmid, it's easier to enter an RRID or an Addgene Catalog Number to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.
If you still could not find your plasmid in the search results, please help us by registering it into the system — it's easy. Register it with Addgene.
Welcome to the dkNET Resources search. From here you can search through a compilation of resources used by dkNET and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that dkNET has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.
If you have an account on dkNET then you can log in from here to get additional features in dkNET such as Collections, Saved Searches, and managing Resources.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
If you are logged into dkNET you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the facets that you can filter the data by.
If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.