Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

Plasmids are provided by Addgene and DGRC.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Mentions:yes (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

32,424 Results - per page

Show More Columns | Download Top 1000 Results

Plasmid Name Proper Citation Insert Name Organism Bacterial Resistance Defining Citation Comments Vector Backbone Description Relevant Mutation Record Last Update Mentions Count
LCMV:ECFP(loxP)(FRT)MCS
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31377 ECFP(loxP)MCS Ampicillin PMID:11376165 Cre and Flp reporter: from blue protein fluorescence to gene of interested inserted into multiple cloning site (MCS) Backbone Size:4100; Vector Backbone:pCS2+; Vector Types:Mammalian Expression, Cre/Lox, Flp/FRT; Bacterial Resistance:Ampicillin 2026-08-15 01:13:31 1
pCVL Traffic Light Reporter 2.1 (VF2468 ZFN target) Ef1a
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31483 Traffic Light Reporter 2.1 (V2468 zfn target) EF Puro Ampicillin PMID:21743461 Backbone Size:5000; Vector Backbone:pCVL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin Traffic Light 2.0 series have a +3 PEST sequence that aids in degradation of the +3 "gibberishFP" produced by mutNHEJ events. The mCherry sequence has M9S and M16L mutations that reduce background fluorescence from internal start codons. This is what ".1" stands for. 2026-08-15 01:13:32 2
pCVL Traffic Light Reporter 1.1 (Sce target) Ef1a Puro
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_31482 Traffic Light Reporter 1.1 (Sce Target) EF Puro Ampicillin PMID:21743461 Backbone Size:5000; Vector Backbone:pCVL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin mCherry has M9S and M16L mutations. This is what the ".1" means. 2026-08-15 01:13:35 27
pFB-GluCl_cryst
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31488 C. elegans glutamate-gated chloride channel alpha, crystallized construct Caenorhabditis elegans Ampicillin PMID:21572436 Backbone Marker:Invitrogen; Backbone Size:4800; Vector Backbone:pFastbac1; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:36 1
pRsetB-pHRed
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31472 pHRed Synthetic Ampicillin PMID:21631110 Backbone Marker:Invitrogen; Backbone Size:2760; Vector Backbone:pRsetB; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:36 2
pQStrep2-PREI3
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31592 preimplantation protein 3 Homo sapiens Ampicillin PMID:15998469 Please note that there is a small gap between Addgene's quality control sequence and the reference sequence provided by the depositor. The gap is downstream of the ORF and should not affect function. Backbone Size:3460; Vector Backbone:pQStrep2; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:35 1
pCVL SFFV d14GFP EF1s HA.NLS.Sce(opt)
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_31476 SFFV d14 GFP donor EF1s I-SceI Ampicillin PMID:21743461 Backbone Size:5092; Vector Backbone:pCVL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin GFP has 14 amino acids deleted from c terminus 2026-08-15 01:13:35 14
pCVL SFFV d14GFP Donor
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_31475 SFFV d14GFP Ampicillin PMID:21743461 Backbone Size:5516; Vector Backbone:pCVL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin Deleted 14 amino acids on the c terminus of eGFP 2026-08-15 01:13:36 11
pSLIK sh human Rb 1534 hyg
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31500 RB shRNA Homo sapiens Ampicillin The whole sequence for the shRNA including the loop should be from 3872-3931 in the vector: AGCGAAACGATTATCCATTCAAATAGTGAAGCCACAGATGTATTTGAAT The shRNA is downstream of the EGFP GGATAATCGTT pSLIK vector from Ian Frasier Backbone Size:13700; Vector Backbone:pSLIK-EGFP; Vector Types:Mammalian Expression, Lentiviral, RNAi; Bacterial Resistance:Ampicillin The target sequence for shRB 1534 is GAACGATTATCCATTCAAA 2026-08-15 01:13:35 3
pQStrep2-ARPC3
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31580 Actin related protein 2/3 complex, subunit 3 Homo sapiens Ampicillin PMID:15998469 The vector pQTEV is derived from Qiagen pQE-2 and contains an inactive chloramphenicol resistance gene sequence. Please note that Addgene's quality control sequence shows a small deletion in the vector region downstream of insert; the deletion does not affect any features in this construct. Backbone Size:3460; Vector Backbone:pQStrep2; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:33 1
pLS1
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31490 lactose repressor protein Ampicillin PMID:11266612 Parent plasmid was pEMBL9' with insert of extended LacI sequence from pIQ (Hare & Sadler, Gene 3 (1978) 269-278. For expression: E. coli BLIM cells (or any E. coli WITHOUT lactose repressor in the genome or accompanying plasmid) Backbone Size:4540; Vector Backbone:pEMBL9'; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:35 2
pTARA
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31491 RNA polymerase T7 phage Chloramphenicol PMID:10610690 For expression: E. coli CV2 N823D mutation should not affect plasmid function. Backbone Size:5400; Vector Backbone:pBAD33; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol N823D 2026-08-15 01:13:33 5
GFP-Rab5
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31733 Rab5 Drosophila melanogaster Ampicillin PMID:21169635 Backbone Marker:Drosophila Gateway Collection; Vector Backbone:pAGW; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:36 9
GFP-Rab8
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31735 Rab8 Drosophila melanogaster Ampicillin PMID:21169635 Backbone Marker:Drosophila Gateway Collection; Vector Backbone:pAGW; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:39 3
GFP-Rab6
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31734 Rab6 Drosophila melanogaster Ampicillin PMID:21169635 Backbone Marker:Drosophila Gateway Collection; Vector Backbone:pAGW; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:35 1
GFP-Rab10
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31737 Rab10 Drosophila melanogaster Ampicillin PMID:21169635 Backbone Marker:Drosophila Gateway Collection; Vector Backbone:pAGW; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:35 1
pRK5F-ALK5-HA(ecto)
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31720 ALK5 Homo sapiens Ampicillin This construct is beginning from a Signal Peptide of human TbRI/ALK5, followed by a HA tag, the extracellular cDNA sequence of human TbRI/ALK, and ended by a Flag tag. This vector to produces a secreted TbRI/ALK5 extracellular form, with two individual tags on each side. Backbone Size:4716; Vector Backbone:pRK5; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:36 1
LZRS-Rfa
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31601 Chloramphenicol and Ampicillin PMID:15342384 Backbone Marker:Khavari Lab; Backbone Size:11100; Vector Backbone:LZRS-RfA; Vector Types:Retroviral; Bacterial Resistance:Chloramphenicol and Ampicillin 2026-08-15 01:13:37 5
BoNT/A-LC
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31602 BoNT/A LC Ampicillin PMID:18940613 The author states that although the construct is from a toxic protein, it only contains one third of the biologically active protein,i.e., it is inactive and harmless per se, and it does not require BL4 level for its expression/manipulation. Toxic BoNT/A is made of two 'chains' (i.e. polypeptides) linked to each other by one disulfide bond. The light chain (LC) is 50KDa long, whereas the heavy chain (HC) is 100 KDa. The HC is necessary for the toxin to target and enter motorneurons. This construct is the LC of BoNTA, and it completely lacks the HC, so it is unable to intoxicate neurons. Protein sequence of BoNT/A fragment present in this plasmid (corresponds to YP_001386738.1) MSGLEVSFEELRTFGGHDAKFIDSLQENEFRLYYYNKFKDIASTLNKAKSIVGTTASLQYMKNVFKEKYLLSEDTSGKFSVDKLKFDKLYKMLTEIYTEDNFVKFFKVLNRKTYLNFDKAVFKINIVPKVNYTIYDGFNLRNTNLAANFNGQNTEINNMNFTKLKNFT Nucleotide sequence of BoNT/A fragment present in this plasmid based on Addgene's Sanger sequencing results: ATGAGTGGGTTAGAAGTAAGCTTTGAGGAACTTAGAACATTTGGGGGACATGATGCAAAGTTTATAGATAGTTTACAGGAAAACGAATTTCGTCTATATTATTATAATAAGTTTAAAGATATAGCAAGTACACTTAATAAAGCTAAATCAATAGTAGGTACTACTGCTTCATTACAGTATATGAAAAATGTTTTTAAAGAGAAATATCTCCTATCTGAAGATACATCTGGAAAATTTTCGGTAGATAAATTAAAATTTGATAAGTTATACAAAATGTTAACAGAGATTTACACAGAGGATAATTTTGTTAAGTTTTTTAAAGTACTTAACAGAAAAACATATTTGAATTTTGATAAAGCCGTATTTAAGATAAATATAGTACCTAAGGTAAATTACACAATATATGATGGATTTAATTTAAGAAATACAAATTTAGCAGCAAACTTTAATGGTCAAAATACAGAAATTAATAATATGAATTTTACTAAACTAAAAAATTTTACT Backbone Size:0; Vector Backbone:pBN3; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:13:35 1
pDONR223-MCU
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_31726 MCU Homo sapiens Spectinomycin PMID:21685886 *A3T aa residue substitution in MCU, which is not known to affect protein function Backbone Marker:Invitrogen; Backbone Size:2787; Vector Backbone:pDONR223; Vector Types:pDONR Gateway; Bacterial Resistance:Spectinomycin * 2026-08-15 01:13:39 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.

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    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.

  2. Navigation

    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.

  3. Logging in and Registering

    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.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    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.