Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
Species: Homo sapiens
Genetic Insert: PTEN
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:5446; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_10927 Copy
Species: Homo sapiens
Genetic Insert: human C-terminal CoREST, sequence-optimized for insect cells
Vector Backbone Description: Backbone Marker:Geneva Biotech; Vector Backbone:pACEBac1; Vector Types:Insect Expression; Bacterial Resistance:Gentamicin
Defining Citation: PMID:28218430
Proper citation: RRID:Addgene_109159 Copy
Species: Homo sapiens
Genetic Insert: PTEN
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:5446; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_10926 Copy
Species: Homo sapiens
Genetic Insert: DGCR8
Vector Backbone Description: Backbone Size:5283; Vector Backbone:N/A; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:15589161
Proper citation: RRID:Addgene_10921 Copy
Vector Backbone Description: Backbone Size:6967; Vector Backbone:pEMBL8; Vector Types:Mammalian Expression, AAV, CRISPR; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30619914
Proper citation: RRID:Addgene_109314 Copy
Genetic Insert: Mttp gRNA
Vector Backbone Description: Backbone Size:6967; Vector Backbone:pEMBL8; Vector Types:Mammalian Expression, AAV, CRISPR; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30619914
Proper citation: RRID:Addgene_109315 Copy
Vector Backbone Description: Backbone Size:4362; Vector Backbone:pEMBL8; Vector Types:Mammalian Expression, AAV, CRISPR; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30619914
Proper citation: RRID:Addgene_109317 Copy
Species: Mus musculus
Genetic Insert: TCR zeta
Vector Backbone Description: Backbone Marker:Clontech; Backbone Size:4700; Vector Backbone:pEGFPN1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Proper citation: RRID:Addgene_109295 Copy
Species: Mus musculus
Genetic Insert: murine IL-6 promoter
Vector Backbone Description: Backbone Marker:Clontech; Backbone Size:4700; Vector Backbone:pCR2.1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:22820329
Proper citation: RRID:Addgene_109296 Copy
Species: Mus musculus
Genetic Insert: miR-181 c and d
Vector Backbone Description: Vector Backbone:pGC; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Proper citation: RRID:Addgene_109297 Copy
Species: Saccharomyces cerevisiae
Genetic Insert: Flp
Vector Backbone Description: Backbone Marker:Promega; Vector Backbone:pCMVTnT; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:28660316
Proper citation: RRID:Addgene_109167 Copy
Species: Other
Genetic Insert: Multiple Cloning Site and GFP
Vector Backbone Description: Backbone Marker:from PMID 9218713; Vector Backbone:pSUM36; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:22820329
Comments: GFP cloned into pSUM36 in reverse orientation so that it is expressed off the 3' end of the kanamycin cassette.
Proper citation: RRID:Addgene_109288 Copy
Species: Homo sapiens
Genetic Insert: mCherry-KASH
Vector Backbone Description: Vector Backbone:Custom; Vector Types:AAV; Bacterial Resistance:Ampicillin
Defining Citation: PMID:30271673
Proper citation: RRID:Addgene_109321 Copy
Vector Backbone Description: Backbone Marker:from PMID 9218713; Vector Backbone:pSUM36; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Defining Citation: PMID:22820329
Comments: pSUM-kan-MCS1-gfp was modified to flip the BamHI and HindII sites for directional cloning. The optimized translation initiation site (from pGreenTIR) was cloned at the 3' end of the kanamycin cassette.
Proper citation: RRID:Addgene_109289 Copy
Species: Synthetic
Genetic Insert: Ppsp_pIII(P29*); luxAB; PproK_TyrT(Opt, CUA);
Vector Backbone Description: Backbone Marker:David Liu Lab; Vector Backbone:SC101; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:29035361
Proper citation: RRID:Addgene_109260 Copy
Species: Synthetic
Genetic Insert: Ppsp_pIII(P29*, P83*, T177*, Y184*); luxAB; PproK_TyrT(Opt, CUA);
Vector Backbone Description: Backbone Marker:David Liu Lab; Vector Backbone:SC101; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:29035361
Proper citation: RRID:Addgene_109263 Copy
Species: Ruminococcus bromii
Genetic Insert: RupA_C1-A1-T1
Vector Backbone Description: Backbone Marker:Novagen; Backbone Size:5370; Vector Backbone:pET29b; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Proper citation: RRID:Addgene_109255 Copy
Species: Ruminococcus bromii
Genetic Insert: RupA_C2-A2-T2-R
Vector Backbone Description: Backbone Marker:Novagen; Backbone Size:5370; Vector Backbone:pET29b; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin
Proper citation: RRID:Addgene_109256 Copy
Species: Rattus norvegicus
Genetic Insert: neuNT
Vector Backbone Description: Backbone Size:4400; Vector Backbone:pSV2 neo; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:2871941
Comments: See author's map. The neu cDNA was inserted between the HindIII and SmaI sites of pSV2-neo, removing the neo gene. Has normal neu cDNA as in pSV2 neuN with transforming sequence (1899-2387) of pSV2 neuT. Expressed in NIH cells at higher levels than pSV2 neuT.
Proper citation: RRID:Addgene_10918 Copy
Species: Rattus norvegicus
Genetic Insert: neuN
Vector Backbone Description: Backbone Size:4400; Vector Backbone:pSV2 neo; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:2871941
Comments: See author's map. The neu cDNA was inserted between the HindIII and SmaI sites of pSV2-neo, removing the neo gene. Expresses better than pSV2 neuT. Has about 100 nt of 5' untranslated region.
Proper citation: RRID:Addgene_10917 Copy
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 T1D Resources search. From here you can search through a compilation of resources used by T1D and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that T1D 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 T1D then you can log in from here to get additional features in T1D 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:
You can save any searches you perform for quick access to later from here.
We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.
If you are logged into T1D you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the sources that were queried against in your search that you can investigate further.
Here are the categories present within T1D that you can filter your data on
Here are the subcategories present within this category that you can filter your data on
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.