Searching the RRID Resource Information Network
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 |
|||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
pGEX-parkin WT Resource Report Resource Website |
RRID:Addgene_45969 | Parkin | Rattus norvegicus | Ampicillin | PMID:23661642 | Backbone Marker:Amersham; Backbone Size:4966; Vector Backbone:pGEX-6P-1; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | Codon usage optimized for E.coli expression | Addgene | 2026-11-07 01:15:49 | 0 | |
|
pCMV-Luc Resource Report Resource Website 1+ mentions |
RRID:Addgene_45968 | Luciferase | Firefly | Ampicillin | Backbone Marker:Promega; Vector Backbone:pGL3 basic; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:49 | 8 | |||
|
pUAST YFP mouse Rab35 DN Resource Report Resource Website |
RRID:Addgene_46016 | Rab35 | Mus musculus | Ampicillin | PMID:19729655 | Backbone Size:8900; Vector Backbone:pUAST; Vector Types:Insect Expression, Drosophila; Bacterial Resistance:Ampicillin | S22N (dominant negative) | Addgene | 2026-11-07 01:15:50 | 0 | |
|
pCM351 Resource Report Resource Website |
RRID:Addgene_46013 | Ampicillin | PMID:12449384 | This allelic exchange vector is used with Cre expression vectors (Addgene plasmids 45863 or 45864) to generate unmarked mutants in a broad bacterial host range. | Backbone Marker:Lidstrom Lab (PMID 8021187); Backbone Size:6000; Vector Backbone:pAYC61; Vector Types:Cre/Lox; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:50 | 0 | |||
|
pUAST YFP mouse Rab35 WT Resource Report Resource Website |
RRID:Addgene_46014 | Rab35 | Mus musculus | Ampicillin | PMID:19729655 | Backbone Size:8900; Vector Backbone:pUAST; Vector Types:Insect Expression, Drosophila; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:50 | 0 | ||
|
pCAG-TALEN-G-pA Resource Report Resource Website |
RRID:Addgene_45962 | TALEN | Synthetic | Ampicillin | Backbone Size:2500; Vector Backbone:pBluescript; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:49 | 0 | |||
|
pUASP YFP Rab9Fb WT Resource Report Resource Website |
RRID:Addgene_46017 | Rab9Fb | Drosophila melanogaster | Ampicillin | PMID:17409086 | Backbone Size:9939; Vector Backbone:pUASP; Vector Types:Insect Expression, Drosophila; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:50 | 0 | ||
|
pCLX-R4-DEST-R2 Resource Report Resource Website 1+ mentions |
RRID:Addgene_45956 | Chloramphenicol and Ampicillin | PMID:21590398 | More information can be found at http://medweb2.unige.ch/salmon/lentilab/lentivectors.html | Backbone Size:8235; Vector Backbone:pCLX-DEST; Vector Types:Lentiviral; Bacterial Resistance:Chloramphenicol and Ampicillin | Addgene | 2026-11-07 01:15:49 | 3 | |||
|
pENTR-L4-UBI-L1R Resource Report Resource Website 1+ mentions |
RRID:Addgene_45959 | human UBI promoter | Homo sapiens | Kanamycin | PMID:21590398 | More information can be found at http://medweb2.unige.ch/salmon/lentilab/lentivectors.html NOTE: There are some discrepancies between Addgene's quality control sequence and the assembled sequence from the depositor. These differences should not affect plasmid function. | Backbone Marker:Invitrogen; Backbone Size:4777; Vector Backbone:pDONRP4P1R; Vector Types:pENTR plasmid; Bacterial Resistance:Kanamycin | Addgene | 2026-11-07 01:15:49 | 4 | |
|
pGR-L3S2P00 Resource Report Resource Website |
RRID:Addgene_46005 | L3S2P00 Terminator | Synthetic | Ampicillin | PMID:23727987 | Backbone Size:5047; Vector Backbone:pGR; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:50 | 0 | ||
|
pGR Resource Report Resource Website 1+ mentions |
RRID:Addgene_46002 | Ampicillin | PMID:23727987 | This is a reporter plasmid for measuring terminator strength by inserting terminator of interest between the GFP and RFP, expression driven by a single PBAD promoter inducible by arabinose. | Backbone Marker:http://partsregistry.org/partsdb/get_part.cgi?part=pSB1A10; Backbone Size:5191; Vector Backbone:pSB1A10; Vector Types:Bacterial Expression, Synthetic Biology; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:50 | 3 | |||
|
pENTR-L4-pTF-L1R Resource Report Resource Website |
RRID:Addgene_45954 | pTF promoter | Synthetic | Kanamycin | PMID:21761975 | More information can be found at http://medweb2.unige.ch/salmon/lentilab/lentivectors.html | Backbone Marker:Invitrogen; Backbone Size:4777; Vector Backbone:pDONRP4P1R; Vector Types:Gateway Cloning; Bacterial Resistance:Kanamycin | Addgene | 2026-11-07 01:15:49 | 0 | |
|
pCWX-R4-DEST-R2-PGR65 Resource Report Resource Website 1+ mentions |
RRID:Addgene_45953 | Chloramphenicol and Ampicillin | PMID:21761975 | More information can be found at http://medweb2.unige.ch/salmon/lentilab/lentivectors.html NOTE: there is an additional BglII site directly after the stop codon that is not present in the full depositor sequence. | Backbone Size:11023; Vector Backbone:pCWX-DEST-PGR; Vector Types:Lentiviral; Bacterial Resistance:Chloramphenicol and Ampicillin | Addgene | 2026-11-07 01:15:49 | 2 | |||
|
pHsp70-Cas9 Resource Report Resource Website 10+ mentions |
RRID:Addgene_45945 | Codon optimized Cas9 | Kanamycin | PMID:23709638 | For more information on FlyCRISPR plasmids and a list of related plasmids please refer to: https://www.addgene.org/browse/article/6834/. Plasmid 51019: pDsRed-attP (www.addgene.org/51019) can be for generating dsDNA donors for homology-directed repair to replace genes or other genomic sequence with an attP docking site. | Backbone Size:2300; Vector Backbone:pHSS6; Vector Types:CRISPR; Bacterial Resistance:Kanamycin | Silent change from C to A at bp 834 of insert | Addgene | 2026-11-07 01:15:49 | 21 | |
|
pTDpelB-C_sfYFPTwinStrep Resource Report Resource Website |
RRID:Addgene_45944 | synthetic sfYFP (codon usage adapted to P.putida KT2440) | Aequorea victoria | Streptomycin | PMID:23687945 | This plasmid was tested in the Gram-negative soil bacterium Pseudomonas putida KT2440 and Escherichia coli K12 and is especially suited for protein production, affinity purification, protein complex copurification with SPINE (Strep Protein Interaction Experiments) or (co-)localization studies. Due to the broad host range of the RK2 origin of replication, the plasmid facilitates experimental verification of hypothetical proteins and protein production yield assessment in different expression hosts possibly including new isolates. The Supplementary Table S1 in the following publication lists approximately 30 strains in which the RK2 origin of replication should be functional. Silva-Rocha et al., The Standard European Vector Architecture (SEVA): a coherent platform for the analysis and deployment of complex prokaryotic phenotypes. Nucleic Acids Research 2013, 41:D666-675. http://nar.oxfordjournals.org/content/41/D1/D666.long | Backbone Marker:Dammeyer et al. 2013; Vector Backbone:pTDpelB-CTwinStrep; Vector Types:Bacterial Expression; Bacterial Resistance:Streptomycin | Addgene | 2026-11-07 01:15:49 | 0 | |
|
pU6-BbsI-chiRNA Resource Report Resource Website 100+ mentions |
RRID:Addgene_45946 | U6-BbsI-chiRNA | Ampicillin | PMID:23709638 | For more information on FlyCRISPR plasmids please refer to: https://www.addgene.org/browse/article/6834/. Plasmid 51019: pDsRed-attP (www.addgene.org/51019) can be for generating dsDNA donors for homology-directed repair to replace genes or other genomic sequence with an attP docking site. Please note the F1 ori is in the (+) orientation, rather than the (-) orientation shown in the assembled full sequence. | Backbone Marker:Agilent; Backbone Size:2958; Vector Backbone:pBS-SK(+); Vector Types:Insect Expression, CRISPR; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:15:49 | 191 | ||
|
pTDpelB-NTwinStrep Resource Report Resource Website |
RRID:Addgene_45940 | Streptomycin | PMID:23687945 | This plasmid was tested in the Gram-negative soil bacterium Pseudomonas putida KT2440 and Escherichia coli K12 and is especially suited for protein production, affinity purification, protein complex copurification with SPINE (Strep Protein Interaction Experiments) or (co-)localization studies. Due to the broad host range of the RK2 origin of replication, the plasmid facilitates experimental verification of hypothetical proteins and protein production yield assessment in different expression hosts possibly including new isolates. The Supplementary Table S1 in the following publication lists approximately 30 strains in which the RK2 origin of replication should be functional. Silva-Rocha et al., The Standard European Vector Architecture (SEVA): a coherent platform for the analysis and deployment of complex prokaryotic phenotypes. Nucleic Acids Research 2013, 41:D666-675. http://nar.oxfordjournals.org/content/41/D1/D666.long | Backbone Marker:SEVA (de Lorenzo Lab); Vector Backbone:pSEVA424; Vector Types:Bacterial Expression; Bacterial Resistance:Streptomycin | Addgene | 2026-11-07 01:15:49 | 0 | |||
|
EHD2-T72A-mEGFP Resource Report Resource Website |
RRID:Addgene_45934 | Eps-15 homology domain-containing protein2 | Homo sapiens | Kanamycin | PMID:22505029 | Backbone Marker:Clontech/ custom-made; Backbone Size:4745; Vector Backbone:pmEGFP-N-DEST; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin | T 72 changed to A (T72A) | Addgene | 2026-11-07 01:15:49 | 0 | |
|
EHD2-mCherry Resource Report Resource Website |
RRID:Addgene_45933 | Eps-15 homology domain-containing protein2 | Homo sapiens | Kanamycin | PMID:22505029 | Backbone Marker:Clontech/ custom-made; Backbone Size:4736; Vector Backbone:pmEGFP-N-DEST; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin | Addgene | 2026-11-07 01:15:49 | 0 | ||
|
pTD-NStrepHis Resource Report Resource Website 1+ mentions |
RRID:Addgene_45936 | Streptomycin | PMID:23687945 | This plasmid was tested in the Gram-negative soil bacterium Pseudomonas putida KT2440 and Escherichia coli K12 and is especially suited for protein production, affinity purification, protein complex copurification with SPINE (Strep Protein Interaction Experiments) or (co-)localization studies. Due to the broad host range of the RK2 origin of replication, the plasmid facilitates experimental verification of hypothetical proteins and protein production yield assessment in different expression hosts possibly including new isolates. The Supplementary Table S1 in the following publication lists approximately 30 strains in which the RK2 origin of replication should be functional. Silva-Rocha et al., The Standard European Vector Architecture (SEVA): a coherent platform for the analysis and deployment of complex prokaryotic phenotypes. Nucleic Acids Research 2013, 41:D666-675. http://nar.oxfordjournals.org/content/41/D1/D666.long | Backbone Marker:SEVA (de Lorenzo Lab); Vector Backbone:pSEVA424; Vector Types:Bacterial Expression; Bacterial Resistance:Streptomycin | Addgene | 2026-11-07 01:15:49 | 1 |
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 RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that RRID 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 RRID then you can log in from here to get additional features in RRID 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 RRID 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.
