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 |
||||
|---|---|---|---|---|---|---|---|---|---|---|
|
pGGN000 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48865 | Chloramphenicol and Kanamycin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. It serves to create intermediate supermodules with plant resistance cassettes. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 358-368bp BsaI site #2 = 1796-1806bp | Backbone Size:2051; Vector Backbone:pENTR1A; Vector Types:Golden Gate Compatible cloning vector; Bacterial Resistance:Chloramphenicol and Kanamycin | 2026-08-15 01:15:54 | 1 | |||
|
pGGH000 Resource Report Resource Website |
RRID:Addgene_48862 | Chloramphenicol and Ampicillin | PMID:24376629 | This plasmid is designed to take up inserts for future Golden Gate cloning using the BsaI enzyme. The 5' BsaI overhang can be exchanged using HindIII and BamHI. The 3' BsaI overhang can be exchanged using KpnI and EcoRI. BamHI and KpnI sites as well as the double XcmI sites can also be used as alternative insert cloning sites, instead of using BsaI. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp BsaI site #2 = 3315-3325bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate Compatible cloning vector; Bacterial Resistance:Chloramphenicol and Ampicillin | 2026-08-15 01:15:54 | 0 | |||
|
pGGY003 Resource Report Resource Website |
RRID:Addgene_48867 | Chloramphenicol and Gentamicin | PMID:24376629 | This plasmid is designed as destination vector for Golden Gate cloning using the BsaI enzyme. The 5' BsaI overhang can be exchanged using KpnI and EcoRI. The 3' BsaI overhang can be exchanged using XhoI and XbaI. There is also a a NotI-PacI-SgsI-SfaAI-KpnI MCS in front of the A-overhang and an XbaI-PaeI MCS after the G-overhang. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 602-612bp BsaI site #2 = 2040-2050bp | Backbone Size:2492; Vector Backbone:pGreenII; Vector Types:Golden Gate compatible plant transformation vector; Bacterial Resistance:Chloramphenicol and Gentamicin | 2026-08-15 01:15:54 | 0 | |||
|
EcNGRfEfC-R10S1C8 Resource Report Resource Website |
RRID:Addgene_48900 | galK::fadBp-CAT, mutS::bla, fadE265G>T/268delG | Spectinomycin | strain contains pZE41 backbone (specR), fadD, tesA' galK::fadBp-CAT, mutS::bla, fadE265G>T/268delG | Vector Backbone:pZE41 backbone (specR), fadD, tesA'; Vector Types:; Bacterial Resistance:Spectinomycin | 2026-08-15 01:15:54 | 0 | |||
|
pGGY001 Resource Report Resource Website |
RRID:Addgene_48866 | Chloramphenicol and Gentamicin | PMID:24376629 | This plasmid is designed as destination vector for Golden Gate cloning using the BsaI enzyme. The 5' BsaI overhang can be exchanged using KpnI and EcoRI. The 3' BsaI overhang can be exchanged using XhoI and XbaI. There is also a a NotI-PacI-SgsI-SfaAI-KpnI MCS in front of the A-overhang and an XbaI-PaeI MCS after the G-overhang. Please note that a transposon insertion is present in the chloramphenicol resistance promoter. This insertion does not interfere with plasmid function. There is an additional BsaI site at bp# 1889-1894 which is irrelevant for GreenGate reactions with this plasmid. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 640-650bp transposon integration = 747-2077bp BsaI site #2 = 3414-3419bp | Backbone Size:2492; Vector Backbone:pGreenII; Vector Types:Golden Gate compatible plant transformation vector; Bacterial Resistance:Chloramphenicol and Gentamicin | 2026-08-15 01:15:55 | 0 | |||
|
pGGF000 Resource Report Resource Website |
RRID:Addgene_48861 | Chloramphenicol and Ampicillin | PMID:24376629 | This plasmid is designed to take up inserts for future Golden Gate cloning using the BsaI enzyme. The 5' BsaI overhang can be exchanged using HindIII and BamHI. The 3' BsaI overhang can be exchanged using KpnI and EcoRI. BamHI and KpnI sites as well as the double XcmI sites can also be used as alternative insert cloning sites, instead of using BsaI. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp BsaI site #2 = 3315-3325bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate Compatible cloning vector; Bacterial Resistance:Chloramphenicol and Ampicillin | 2026-08-15 01:15:54 | 0 | |||
|
pGGE000 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48860 | Chloramphenicol and Ampicillin | PMID:24376629 | This plasmid is designed to take up inserts for future Golden Gate cloning using the BsaI enzyme. The 5' BsaI overhang can be exchanged using HindIII and BamHI. The 3' BsaI overhang can be exchanged using KpnI and EcoRI. BamHI and KpnI sites as well as the double XcmI sites can also be used as alternative insert cloning sites, instead of using BsaI. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp BsaI site #2 = 3315-3325bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate Compatible cloning vector; Bacterial Resistance:Chloramphenicol and Ampicillin | 2026-08-15 01:15:54 | 2 | |||
|
pGGE003 Resource Report Resource Website |
RRID:Addgene_48854 | At1g04880 terminator | Arabidopsis thaliana | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp At1g04480 terminator = 2252-2758bp BsaI site #2 = 2759-2769bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 0 | |
|
pGGD005 Resource Report Resource Website |
RRID:Addgene_48853 | Linker:BFP | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp linker-BFP = 2252-3066bp BsaI site #2 = 3067-3077bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 0 | |
|
pGGG002 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48851 | H-A adapter - short | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp H-A adapter = 2252-2271bp BsaI site #2 = 2272-2282bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 1 | |
|
pGGA000 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48856 | Chloramphenicol and Ampicillin | PMID:24376629 | This plasmid is designed to take up inserts for future Golden Gate cloning using the BsaI enzyme. The 5' BsaI overhang can be exchanged using HindIII and BamHI. The 3' BsaI overhang can be exchanged using KpnI and EcoRI. BamHI and KpnI sites as well as the double XcmI sites can also be used as alternative insert cloning sites, instead of using BsaI. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp BsaI site #2 = 3315-3325bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate Compatible cloning vector; Bacterial Resistance:Chloramphenicol and Ampicillin | 2026-08-15 01:15:54 | 4 | |||
|
pGGG001 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48850 | F-H adapter - short | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp F-H adapter = 2252-2271bp BsaI site #2 = 2272-2282bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 1 | |
|
pGGF012 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48849 | pMAS::SulfadiazineR::t35S | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp Sulfadiazine resistance cassette with MAS promoter and 35S terminator = 2252-3882bp BsaI site #2 = 3883-3893bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | internal BsaI recognition sites in SulfR removed by silent substitutions | 2026-08-15 01:15:54 | 1 |
|
pGGF008 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48848 | pNOS::BastaR::tNOS | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp BASTA resistance cassette with NOS promoter and terminator = 2252-3334bp BsaI site #2 = 3335-3345bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | chi sequence in BastaR removed by silent substitution | 2026-08-15 01:15:54 | 1 |
|
pGGE009 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48841 | UBQ10 terminator | Arabidopsis thaliana | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp UBQ10 terminator = 2252-2879bp BsaI site #2 = 2880-2890bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 3 | |
|
pGGD007 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48837 | linker:nuclear localization signal | Arabidopsis thaliana | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp linker-nuclear localization signal = 2252-2550bp BsaI site #2 = 2551-2561bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 1 | |
|
pGGC026 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48831 | 3xmCherry | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp 3x mCherry coding sequence = 2252-4491bp BsaI site #2 = 4492-4502bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 2 | |
|
pGGC025 Resource Report Resource Website |
RRID:Addgene_48830 | 3xGFP | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp 3x GFP coding sequence = 2252-4518bp BsaI site #2 = 4519-4529bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 0 | |
|
pGGD006 Resource Report Resource Website |
RRID:Addgene_48836 | SV40 NLS | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp SV40 nuclear localization signal = 2252-2277bp BsaI site #2 = 2278-2288bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 0 | |
|
pGGD003 Resource Report Resource Website 1+ mentions |
RRID:Addgene_48835 | Linker-mCherry | Synthetic | Ampicillin | PMID:24376629 | This plasmid is designed for Golden Gate cloning using the BsaI enzyme. Plasmid Features (listed as bp in full plasmid sequence): BsaI site #1 = 2241-2251bp linker-mCherry = 2252-3063bp BsaI site #2 = 3064-3074bp | Backbone Size:2686; Vector Backbone:pUC19; Vector Types:Golden Gate compatible cloning vector; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:54 | 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 dkNET Resources search. From here you can search through a compilation of resources used by dkNET and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that dkNET 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 dkNET then you can log in from here to get additional features in dkNET 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 dkNET 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.
The NIDDK Information Network (dkNET) serves the needs of basic and clinical investigators by providing seamless access to large pools of data and research resources relevant to the mission of The National Institute of Diabetes Digestive and Kidney Diseases (NIDDK). dkNET is hosted at University of California San Diego, and is supported by NIH NIDDK grant U24DK097771.
Email: info_at_ dknet.org
