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 |
|||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
aMHC-mCherry-Rex-Blasticidin Resource Report Resource Website 1+ mentions |
RRID:Addgene_21228 | alpha myosin heavy chain promoter | Mus musculus | Ampicillin | PMID:19352491 | There is an extra C in the promoter sequence when compared to the available reference sequence in NCBI. The mismatch is due to older sequencing artifact of an erroneous insertion of a "C" adjacent to "GGG". The construct should be correct. | Backbone Size:7338; Vector Backbone:SMPU; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:00 | 5 | |
|
pRosa26-DEST Resource Report Resource Website 10+ mentions |
RRID:Addgene_21189 | GateWay conversion cassette | Chloramphenicol and Ampicillin | PMID:19014667 | pRosa26-DEST was made by inserting a GateWay conversion cassette into the XhoI site of pBigT, followed by transfer of PacI / AscI fragment of the resulting vector to the pRosa26-PA vector (see http://www.biomedcentral.com/1471-213X/1/4 for details on these vectors). The resulting vector resembles the construct that was used for the R26R Cre reporter mouse made by Phil Soriano in which the expression of lacZ is coupled to the endogenous Rosa26 locus via a splice acceptor site, but only after removal of the lox-STOP-lox cassette (which is actually the neo-R cassette used during the targeting). The only thing changed from the pBigT vectors and the R26R reporter is the cloning strategy, so the resulting knock-in should be as good as these systems, and as good (or as bad) as the use of the Rosa26 locus in any situation. Stbl3 cells are advisable to use after users have done the LR recombination reaction. See http://www.hgu.mrc.ac.uk/people/n.hastie_rosa.html for more information and protocols for this plasmid. Further advice from the depositing lab: "Grow single colonies in Amp + Cam at 30 C, definitively not 37. Including the Cam should ensure that spontaneous recombinants that loose the Gateway cassette don't survive... - Do minipreps and test with the double digest PacI / AscI. This should give 4.9 kb + 9.8 kb. If this is okay, the vector should be okay" Please note that there are discrepancies between Addgene's quality control sequence and the theoretical sequence supplied by the depositing lab. These discrepancies should not affect the function of the construct. | Backbone Size:14820; Vector Backbone:pRosa26-PA; Vector Types:Mammalian Expression; Bacterial Resistance:Chloramphenicol and Ampicillin | Addgene | 2026-09-26 02:29:59 | 18 | ||
|
GFP-C1-CAMKIIalpha-T286A Resource Report Resource Website 1+ mentions |
RRID:Addgene_21220 | CAMKIIalpha-T286A | Rattus norvegicus | Kanamycin | PMID:10102820 | Backbone Marker:Clontech; Backbone Size:0; Vector Backbone:C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin | T286A (Lab plasmid KS 0003). | Addgene | 2026-09-26 02:30:00 | 1 | |
|
GFP-C1-CAMKIIalpha Resource Report Resource Website 10+ mentions |
RRID:Addgene_21226 | CAMKIIalpha | Rattus norvegicus | Kanamycin | PMID:9768845 | Backbone Marker:Clontech; Backbone Size:4725; Vector Backbone:C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin | Lab plasmid KS 0001. | Addgene | 2026-09-26 02:30:00 | 10 | |
|
PL-SIN-EOS-S(4+)-EGFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_21317 | Enhanced Green Fluorescence Protein | Ampicillin | PMID:19404254 | EGFP driven by EOS-S(4+) promoter. PL-SIN lentiviral vector (Buzina et al., PLoS Genetics, 2008) requires Tat cDNA for lentivirus production, as well as other packaging cDNAs (Gag/pol, Rev, and VSV-G). | Backbone Marker:Buzina et al., PLoS Genetics, 2008; Backbone Size:6531; Vector Backbone:PL-SIN lentiviral vector; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 1 | ||
|
pMXs-mRFP1 Resource Report Resource Website 1+ mentions |
RRID:Addgene_21315 | monomeric Red Fluorescence Protein 1 | Ampicillin | PMID:19404254 | mRFP1 (maximum Excitation wave length, 584 nm; maximum Emission wave length, 607 nm). pMXs MoMLV-based retroviral vector from Dr. Toshio Kitamura (Institute of Medical Science, University of Tokyo). | Backbone Size:4582; Vector Backbone:pMXs MoMLV-based retroviral vector; Vector Types:Mammalian Expression, Retroviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 5 | ||
|
Axin2 probe Resource Report Resource Website 1+ mentions |
RRID:Addgene_21277 | Axin2 | Mus musculus | Ampicillin | PMID:11809808 | Tong DNA #94. The DNA is a HinDIII fragment of mouse Axin2 (nucleotides 1-2397) in pBluescript-KS. The antisense and sense Axin2 riboprobes were made by linearizing this plasmid with NotI or SalI and transcribing with T3 or T7 RNA polymerase, respectively. List of DNAs says " ~2 kb DIII fragment of Axin2 (1-2397) in pBS-KS”. | Backbone Marker:Stratagene; Backbone Size:3000; Vector Backbone:pBluescript II KS; Vector Types:For riboprobe synthesis; Bacterial Resistance:Ampicillin | cDNA bp 1774 to 2787 | Addgene | 2026-09-26 02:30:00 | 4 |
|
Axin2-luciferase Resource Report Resource Website 1+ mentions |
RRID:Addgene_21275 | Axin2 promoter | Mus musculus | Ampicillin | PMID:11809808 | A 5.6-kb DNA fragment containing the Axin2 promoter, exon 1, intron 1, and part of exon 2 was subcloned from a mouse BAC clone and sequenced. In Author's map, exons are shown as gray boxes, and the sequence is numbered with bp 1 corresponding to the start of the cDNA sequence. Eight conserved Tcf/LEF binding sites (underlined and designated T1 to T8) were identified. | Backbone Marker:Promega; Backbone Size:4800; Vector Backbone:pGL3-Basic; Vector Types:Mammalian Expression, Luciferase; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:00 | 7 | |
|
PL-SIN-EOS-S(4+)-EiP Resource Report Resource Website 1+ mentions |
RRID:Addgene_21314 | Enhanced Green Fluorescence Protein, Puromycin resistance gene | Ampicillin | PMID:19404254 | EGFP and Puro resistance genes driven by EOS-S(4+) promoter. PL-SIN lentiviral vector (Buzina et al., PLoS Genetics, 2008) requires Tat cDNA for lentivirus production, as well as other packaging cDNAs (Gag/pol, Rev, and VSV-G). | Backbone Marker:Buzina et al., PLoS Genetics, 2008; Backbone Size:6626; Vector Backbone:PL-SIN lentiviral vector; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 5 | ||
|
Myc-Axin2 Resource Report Resource Website 1+ mentions |
RRID:Addgene_21279 | Axin2 | Mus musculus | Ampicillin | PMID:11809808 | Backbone Size:4300; Vector Backbone:pCS2+MT; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:00 | 2 | ||
|
pcDNA-FIH1 Resource Report Resource Website 1+ mentions |
RRID:Addgene_21399 | HIF1AN | Homo sapiens | Ampicillin | PMID:12615973 | Backbone Marker:Invitrogen; Backbone Size:5446; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 5 | ||
|
PL-SIN-Nanog-EGFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_21321 | Enhanced Green Fluorescence Protein | Ampicillin | PMID:19404254 | EGFP driven by Nanog promoter. PL-SIN lentiviral vector (Buzina et al., PLoS Genetics, 2008) requires Tat cDNA for lentivirus production, as well as other packaging cDNAs (Gag/pol, Rev, and VSV-G). | Backbone Marker:Buzina et al., PLoS Genetics, 2008; Backbone Size:6531; Vector Backbone:PL-SIN lentiviral vector; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 7 | ||
|
pCS2-MT mouse Axin (Axin MTFu1) Resource Report Resource Website 1+ mentions |
RRID:Addgene_21287 | Axin | Mus musculus | Ampicillin | PMID:9230313 | Backbone Size:4300; Vector Backbone:pCS2+MT; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:00 | 3 | ||
|
PL-SIN-EF1α-EGFP Resource Report Resource Website 10+ mentions |
RRID:Addgene_21320 | Enhanced Green Fluorescence Protein | Ampicillin | PMID:19404254 | EGFP driven by ubiquitous EF1α promoter. PL-SIN lentiviral vector (Buzina et al., PLoS Genetics, 2008) requires Tat cDNA for lentivirus production, as well as other packaging cDNAs (Gag/pol, Rev, and VSV-G). | Backbone Marker:Buzina et al., PLoS Genetics, 2008; Backbone Size:6881; Vector Backbone:PL-SIN lentiviral vector; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 13 | ||
|
TRX1 His C32S C35S Resource Report Resource Website 1+ mentions |
RRID:Addgene_21286 | TRX1 | Homo sapiens | Ampicillin | PMID:12089063 | Backbone Size:5400; Vector Backbone:pcDNA3-His; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | C32S C35S | Addgene | 2026-09-26 02:30:00 | 2 | |
|
TRX1 flag C35S Resource Report Resource Website 1+ mentions |
RRID:Addgene_21285 | TRX1 | Homo sapiens | Ampicillin | PMID:12089063 | Backbone Size:5400; Vector Backbone:pcDNA3-FLAG; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | C35S | Addgene | 2026-09-26 02:30:00 | 4 | |
|
pBSKS Notch4 Resource Report Resource Website 1+ mentions |
RRID:Addgene_21325 | Notch4 | Mus musculus | Ampicillin | PMID:8681805 | Backbone Marker:Stratagene; Backbone Size:2900; Vector Backbone:pBSKS; Vector Types:Cloning Vector; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 1 | ||
|
pHR'-ROMK1-CITE-GFP Resource Report Resource Website 1+ mentions |
RRID:Addgene_21322 | ROMK1 | Rattus norvegicus | Ampicillin | PMID:10938328 | Backbone Marker:Didier Trono; Backbone Size:10000; Vector Backbone:pHR'; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 1 | ||
|
TRX1 flag C32S Resource Report Resource Website 1+ mentions |
RRID:Addgene_21284 | TRX1 | Homo sapiens | Ampicillin | PMID:12089063 | Backbone Size:5400; Vector Backbone:pcDNA3-FLAG; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | C32S | Addgene | 2026-09-26 02:30:00 | 3 | |
|
pHIV-Luciferase Resource Report Resource Website 10+ mentions |
RRID:Addgene_21375 | Ampicillin | The HIV-Luciferase plasmid encodes a self-inactivating lentiviral construct that was cloned by removing the U6-TATAlox-CMVie-EGFP-TATAlox- WPRE content of pSICO (Ventura et al., 2004), and adding the EF1-alpha promoter, a multiple cloning site (MCS), an internal ribosome entry site (IRES) and Luciferase. A cDNA can be cloned into the MCS (NotI, EcoRI, SmaI, and BamHI sites) to enable bicistronic expression with luciferase. This construct has not been published. NOTE: Addgene's stock is missing bp 6102-6190 compared to the original depositor's sequence. This deletion may affect some restriction sites, but not plasmid function. | Backbone Size:8713; Vector Backbone:pSICO; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-09-26 02:30:01 | 32 |
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.