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

  • Issues Status:no known issues (facet)

Facets


Recent searches

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

740,584 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
pDN614
 
Resource Report
Resource Website
RRID:Addgene_175374 Ampicillin PMID:34599813 This plasmid was generated by modification of plasmid pRS404 (Sikorski & Hieter, 1989, Genetics 122:19-27) by insertion of CEN6/ARSH4 low copy S. cerevisiae replication and partitioning locus with flanking restriction enzyme cut sites (AatII) and flanking LoxP sites. bioRxiv pre-print 367219: Rapid conversion of replicating and integrating Saccharomyces cerevisiae plasmid vectors via Cre recombinase https://doi.org/10.1101/2020.11.03.367219 Backbone Size:4887; Vector Backbone:pDN614; Vector Types:Yeast Expression, Cre/Lox; Bacterial Resistance:Ampicillin 2026-08-15 01:10:49 0
pDN616
 
Resource Report
Resource Website
RRID:Addgene_175376 Ampicillin PMID:34599813 This plasmid was generated by modification of plasmid pRS406 (Sikorski & Hieter, 1989, Genetics 122:19-27) by insertion of CEN6/ARSH4 low copy S. cerevisiae replication and partitioning locus with flanking restriction enzyme cut sites (AatII) and flanking LoxP sites. bioRxiv pre-print 367219: Rapid conversion of replicating and integrating Saccharomyces cerevisiae plasmid vectors via Cre recombinase https://doi.org/10.1101/2020.11.03.367219 Backbone Size:4985; Vector Backbone:pDN616; Vector Types:Yeast Expression, Cre/Lox; Bacterial Resistance:Ampicillin 2026-08-15 01:10:49 0
pDN625
 
Resource Report
Resource Website
RRID:Addgene_175379 Ampicillin PMID:34599813 This plasmid was generated by modification of plasmid pRS405 (Sikorski & Hieter, 1989, Genetics 122:19-27) by insertion of 2 micron high copy S. cerevisiae replication and partitioning locus with flanking restriction enzyme cut sites (AatII) and flanking LoxP sites. bioRxiv pre-print 367219: Rapid conversion of replicating and integrating Saccharomyces cerevisiae plasmid vectors via Cre recombinase https://doi.org/10.1101/2020.11.03.367219 Backbone Size:6914; Vector Backbone:pDN625; Vector Types:Yeast Expression, Cre/Lox; Bacterial Resistance:Ampicillin 2026-08-15 01:10:50 0
pDN525
 
Resource Report
Resource Website
RRID:Addgene_175371 Ampicillin PMID:34599813 This plasmid was generated by modification of plasmid pRS405 (Sikorski & Hieter, 1989, Genetics 122:19-27) by insertion of 2 micron high copy S. cerevisiae replication and partitioning locus with flanking restriction enzyme cut sites (AatII, AvrII, and SphI). bioRxiv pre-print 367219: Rapid conversion of replicating and integrating Saccharomyces cerevisiae plasmid vectors via Cre recombinase https://doi.org/10.1101/2020.11.03.367219 Backbone Size:6865; Vector Backbone:pDN525; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:10:49 0
pExpreS2-1-CR-PA-10H-SIII
 
Resource Report
Resource Website
RRID:Addgene_175447 Bleocin (Zeocin) PMID:35600892 This plasmid is designed for use with the ExpreS2 Platform from ExpreS2ion Biotechnologies. It is intended to be used with the ExpreS2ion cells and media which can be obtained directly from the ExpreS2ion website. Backbone Marker:ExpreS2ion Biotechnologies; Backbone Size:3156; Vector Backbone:pExpreS2-1; Vector Types:Insect Expression; Bacterial Resistance:Bleocin (Zeocin) 2026-08-15 01:10:50 0
CD44I-c001
 
Resource Report
Resource Website
RRID:Addgene_175448 CD44 Homo sapiens Kanamycin Ligation-independent cloning 5' site GTACTTCCAATCCAT; 3' site TATCCACCTTTACT. Gileadi lab uses BL21(DE3)-R3-pRARE2 cells for expression. Vector Backbone:pNIC28-Bsa4; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:10:50 0
CD44I-c011
 
Resource Report
Resource Website
RRID:Addgene_175449 CD44 Homo sapiens Kanamycin Ligation-independent cloning 5' site GTACTTCCAATCCAT; 3' site TATCCACCTTTACT. Gileadi lab uses BL21(DE3)-R3-pRARE2 cells for expression. Vector Backbone:pNIC-CTH0; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:10:50 0
pAAV-VTKS5-TVA-eGFP-N2cG
 
Resource Report
Resource Website
RRID:Addgene_175440 TVA-P2A-eGFP-P2A-N2cG Synthetic Ampicillin PMID:34758329 Backbone Marker:Jordane Dimidschstein (Addgene plasmid # 170856); Vector Backbone:pAAV-VTKS5; Vector Types:AAV, Cre/Lox; Bacterial Resistance:Ampicillin 2026-08-15 01:10:50 0
pExpreS2-1-C3-10H-SIII
 
Resource Report
Resource Website
RRID:Addgene_175444 Bleocin (Zeocin) PMID:35600892 This plasmid is designed for use with the ExpreS2 Platform from ExpreS2ion Biotechnologies. It is intended to be used with the ExpreS2ion cells and media which can be obtained directly from the ExpreS2ion website. Backbone Marker:ExpreS2ion Biotechnologies; Backbone Size:2763; Vector Backbone:pExpreS2-1; Vector Types:Insect Expression; Bacterial Resistance:Bleocin (Zeocin) 2026-08-15 01:10:50 0
pExpreS2-1-C3-PA
 
Resource Report
Resource Website
RRID:Addgene_175446 Bleocin (Zeocin) PMID:35600892 This plasmid is designed for use with the ExpreS2 Platform from ExpreS2ion Biotechnologies. It is intended to be used with the ExpreS2ion cells and media which can be obtained directly from the ExpreS2ion website. Backbone Marker:ExpreS2ion Biotechnologies; Backbone Size:3156; Vector Backbone:pExpreS2-1; Vector Types:Insect Expression; Bacterial Resistance:Bleocin (Zeocin) 2026-08-15 01:10:50 0
RS314-SN
 
Resource Report
Resource Website
RRID:Addgene_17539 Gal1-p53 Homo sapiens Ampicillin PMID:7597081 RS314-SN contains wild type p53 driven by the Gal1 promoter (Gal1-p53). Backbone Size:4800; Vector Backbone:pRS314; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:10:50 0
pAAV-VTKS2-TVA-eGFP-N2cG
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_175439 TVA-P2A-eGFP-P2A-N2cG Synthetic Ampicillin PMID:34758329 Backbone Marker:Jordane Dimidschstein (Addgene plasmid # 170853); Vector Backbone:pAAV-VTKS2; Vector Types:AAV, Cre/Lox; Bacterial Resistance:Ampicillin 2026-08-15 01:10:50 3
pBabe B-Raf V600E
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_17544 B-Raf Homo sapiens Ampicillin PMID:17699719 Backbone Size:5200; Vector Backbone:pBabe-puro; Vector Types:Mammalian Expression, Retroviral; Bacterial Resistance:Ampicillin V600E 2026-08-15 01:10:50 12
p5154
 
Resource Report
Resource Website
RRID:Addgene_175390 Ampicillin PMID:35361849 We recommend this plasmid for the generation of the DNA donor when the inserted transgene size is <15kb. For larger insertions, we recommend the low-copy plasmid p5155 (175391). Depending on the nature of the sequence cloned into this plasmid, it may be beneficial to grow using NEB Stable, at 30C. However, just to maintain p5154 alone, DH5alpha is adequate (though we generally use DH10Beta). Backbone Marker:Genscript; Backbone Size:2686; Vector Backbone:pUC18; Vector Types:Mouse Targeting, Cloning vector, to be used to deliver transgene into mice with dual heterologous Bxb1 attP sites; Bacterial Resistance:Ampicillin 2026-08-15 01:10:49 0
Myc-Foxo1 LAALL (pCMV5)
 
Resource Report
Resource Website
RRID:Addgene_17548 Foxo1 LAALL Mus musculus Ampicillin Backbone Size:4657; Vector Backbone:pCMV5; Vector Types:Mammalian Expression, RNAi; Bacterial Resistance:Ampicillin LAALL (K460A; E461A) 2026-08-15 01:10:50 0
p5155
 
Resource Report
Resource Website
RRID:Addgene_175391 Kanamycin PMID:35361849 We recommend this low-copy plasmid for the generation of donor DNA when the inserted transgene size is >15kb. For smaller transgene insertions, we recommend the high-copy plasmid p5154 (Addgene 175390). Backbone Marker:Genscript; Backbone Size:4361; Vector Backbone:pBR322; Vector Types:Mouse Targeting, Cloning vector, to be used to deliver transgene into mice with dual heterologous Bxb1 attP sites; Bacterial Resistance:Kanamycin 2026-08-15 01:10:49 0
EZRA-c004
 
Resource Report
Resource Website
RRID:Addgene_175461 EZR Homo sapiens Kanamycin Ligation-independent cloning 5' site GTACTTCCAATCCAT; 3' site TATCCACCTTTACT. Gileadi lab uses BL21(DE3)-R3-pRARE2 cells for expression. Vector Backbone:pNIC28-Bsa4; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:10:50 0
pH6HTC_NAP1L1-Halo
 
Resource Report
Resource Website
RRID:Addgene_175342 NAP1L1 Homo sapiens Ampicillin Please visit https://doi.org/10.1101/2021.11.08.467743 for bioRxiv preprint. Vector Backbone:pH6HTC_minus_cer-region; Vector Types:Bacterial Expression, Cell Free Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:10:49 0
MDKA-c014
 
Resource Report
Resource Website
RRID:Addgene_175464 MDK Homo sapiens Ampicillin Gileadi lab uses HEK293 cells for expression. Vector Backbone:pHL-Sec; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:10:50 0
MSNA-c000
 
Resource Report
Resource Website
RRID:Addgene_175465 MSN Homo sapiens Kanamycin Ligation-independent cloning 5' site GTACTTCCAATCCAT; 3' site TATCCACCTTTACT. Gileadi lab uses BL21(DE3)-R3-pRARE2 cells for expression. Vector Backbone:pNIC28-Bsa4; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:10:50 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.

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.