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 |
||||
|---|---|---|---|---|---|---|---|---|---|---|
|
pFIN-XOPS-tdTOM-MOPS-GFP Resource Report Resource Website |
RRID:Addgene_44347 | XOPS-tdTOM | Xenopus laevis | Ampicillin | PMID:20517486 | Backbone Marker:LJ Chang; Backbone Size:8760; Vector Backbone:pTY; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | 2026-08-15 01:15:14 | 0 | ||
|
GFP-Intersectin Full Length Resource Report Resource Website |
RRID:Addgene_47407 | Intersectin | Xenopus laevis | Kanamycin | Backbone Marker:Clontech; Vector Backbone:pEGFP; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin | 2026-08-15 01:15:42 | 0 | |||
|
M20 siamois-luciferase p01234 Resource Report Resource Website |
RRID:Addgene_17157 | siamois promoter | Xenopus laevis | Ampicillin | PMID:9308964 | Plasmid History: Constructed by David Kimelman, 6/6/96 XVII p. 98. Notes for Use: The -3.0kb-siamois promoter was directionally cloned into the KpnI and BglII sites of the luciferase reporter vector pGL3B (Promega) upstream of the luciferase ATG. The -0.8kb promoter construct was generated by digesting the -3.0kb/pGL3B construct with KpnI and at an internal EcoRI site to remove 2.2 kb of intervening sequence, filling in with DNA polymerase I large fragment and religating. The Kpn site was lost but the R1 site was regenerated in the ligation. The size of the insert is approximate. Citation: Brannon et al., Gene and Development 11:2359-2370, 1997. | Backbone Marker:promega; Backbone Size:4818; Vector Backbone:pGL3-Basic; Vector Types:Luciferase; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:17 | 0 | |
|
3.8NBetaT-CAT Resource Report Resource Website 1+ mentions |
RRID:Addgene_17146 | Beta-tubulin promoter | Xenopus laevis | Ampicillin | Constructed Rebecca Beach and Paul A. Kreig. 3.8Kb fragment of the Xenopus neural Beta-tubulin promoter inserted (in several cloning steps) into the CAT expression vector pBLCAT3. The 5' end of the neural Beta-tubulin sequence is defined by the natural Xba1 site that occurs in the genomic DNA. The 3' end of the insert is produced by PCR primer located 8bp upstream of hte initiation ATP and 120bp downstream of the transcription start site. The neural Beta-tubulin sequences may be excised as a Hind3 fragment. | Backbone Marker:ATCC; Backbone Size:4300; Vector Backbone:pBLCAT3; Vector Types:; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:16 | 1 | ||
|
M10 NCAM Promoter Resource Report Resource Website |
RRID:Addgene_17147 | NCAM promoter | Xenopus laevis | Ampicillin | Plasmid History: Constructed Paul A. Kreig, July. Note for Use: This construction contains a 1.3 Kb Dra I fragment of the NCAM promoter and should be okay for general neural expression. The fragment is cloned into the Sma I site of Bluescript KS+. The NCAM promoter does not contain a TATA box and transcription starts at numerous sites over about 350 bases. All of the potential start sites are contained in this 1.3 Kb fragment, which ends in the 5' UTR of the NCAM gene. The Dra I fragment starts at the very beginning of the GenBank sequence (starting with aaa) and ends at base 1358 of the GenBank sequence. | Backbone Marker:Stratagene; Backbone Size:3000; Vector Backbone:pBluescript KS(+); Vector Types:Xenopus expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:16 | 0 | ||
|
M11 Cardiac Actin Promoter pCarA Resource Report Resource Website 1+ mentions |
RRID:Addgene_17148 | cardiac actin promoter | Xenopus laevis | Ampicillin | Plasmid History: Constructed by Enrique Amaya. Note for Use: Constructed by cloning the 3270bp KpnI-SalI fragment from DNA#254 (from Tim Mohun) into KpnI-SalI digested pCSKA. | Backbone Size:4000; Vector Backbone:pCSKA; Vector Types:Xenopus expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:18 | 1 | ||
|
M12 pCarGFP2 Resource Report Resource Website |
RRID:Addgene_17149 | cardiac actin promoter | Xenopus laevis | Ampicillin | Plasmid History: Constructed by Enrique Amaya. Note for Use: Generated by inserting the 1Kb HindIII-NotI fragment from pCSGFP2 into HindIII-NotI digested pCarG. This GFP constuct has been modified by Jim Haseloff and Jonathan Pines to be brighter and more soluble that wild-type GFP. Note: Uniques sites are underlined in Author's Map. | Backbone Size:4000; Vector Backbone:pCSKA; Vector Types:Xenopus expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:18 | 0 | ||
|
pGEX-4T-1-Xlrbpa-dsRBD(+6) Resource Report Resource Website |
RRID:Addgene_171548 | Xlrbpa | Xenopus laevis | Ampicillin | PMID:33751023 | Vector Backbone:pGEX-4T-1; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | a six amino acid_TRLTEG_insertion in the L1 region | 2026-08-15 01:10:17 | 0 | |
|
pGEX-4T-1-Xlrbpa Resource Report Resource Website |
RRID:Addgene_171547 | Xlrbpa | Xenopus laevis | Ampicillin | PMID:33751023 | Vector Backbone:pGEX-4T-1; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:17 | 0 | ||
|
-226bp goosecoid luciferase Resource Report Resource Website |
RRID:Addgene_17158 | goosecoid promoter | Xenopus laevis | Ampicillin | PMID:8543150 | Generated by PCR using the 3' primer (nucleotides - 5 to + 12 relative to the transcription start site) and 5' primer to -226. The 3' primer contained a HindIII restriction site at its 5' terminus and the 5' primer contained a BamHI restriction site at its 5' terminus for directional cloning into pOLuc. | Backbone Size:0; Vector Backbone:pOLuc; Vector Types:Luciferase; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:17 | 0 | |
|
-1.5 kb goosecoid luciferase Resource Report Resource Website |
RRID:Addgene_17159 | goosecoid promoter | Xenopus laevis | Ampicillin | PMID:8543150 | The - 1500gsc/Luc reporter was constructed from a blunt-ended EcoRV-PstI 1.5kb Xenopus gsc gene fragment carrying 3 bp of exon 1 and 5'-promoter sequences inserted into the SmaI site of the promoterless luciferase vector pOLuc (de Wet et al. 1987). | Backbone Size:0; Vector Backbone:pOLuc; Vector Types:Luciferase; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:17 | 0 | |
|
M35 Dpr yeast clone Resource Report Resource Website |
RRID:Addgene_17191 | XDpr | Xenopus laevis | Ampicillin | PMID:11970895 | Description: Dpr yeast clone in original prey vector. 1.6kb EcoR1 fragment corresponds to C-terminal 1.2 kb of Xenopus Dpr and 3' UTR in pGAD vector. Reference: Cheyette, B. et al., 2002, Developmental Cell 2: 449-461. | Backbone Marker:Clontech; Backbone Size:8000; Vector Backbone:pGAD; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:20 | 0 | |
|
M36 Dpr C-terminal GST Resource Report Resource Website |
RRID:Addgene_17192 | XDpr | Xenopus laevis | Ampicillin | PMID:11970895 | Description: Coding sequence of original XDpr prey clone (M35) cloned into pGEX vector as a 1.2 kb EcoR1-Xba1 fragment (Xba site is DAM methylated). Reference: Cheyette, B. et al., 2002, Developmental Cell 2: 449-461. | Backbone Size:0; Vector Backbone:pGEX; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:20 | 0 | |
|
M61 pPET28c-Xenopus beta catenin domains R10C Resource Report Resource Website |
RRID:Addgene_17202 | beta catenin | Xenopus laevis | Kanamycin | Description: This is an amino terminal HIS tag, then beta catenin domains R10C, subcloned into BamH1 site. Reference: Made by Ken-Ichi Takemaru. Contains ARM domains 8-10 and C-terminal end of protein (starts with aa519) | Backbone Marker:EMD Biosciences; Backbone Size:5400; Vector Backbone:pET-28 c; Vector Types:Bacterial Expression; Bacterial Resistance:Kanamycin | domains R10C | 2026-08-15 01:10:21 | 0 | |
|
pCS2+-wbp2nlT45A Resource Report Resource Website |
RRID:Addgene_172464 | wbp2nlT45A | Xenopus laevis | Ampicillin | PMID:28663133 | we cloned this plasmid | Backbone Size:4100; Vector Backbone:pCS2+; Vector Types:Xenopus Expression; Bacterial Resistance:Ampicillin | changed Threonine at aa45 to Alanine | 2026-08-15 01:10:24 | 0 |
|
pCS2-xFAM3b.L-HA Resource Report Resource Website |
RRID:Addgene_172852 | xFAM3B.L | Xenopus laevis | Ampicillin | PMID:30209221 | Vector Backbone:pCS2; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:10:28 | 0 | ||
|
XE247 Xenopus CK1 epsilon K to R CS2+ Resource Report Resource Website |
RRID:Addgene_16725 | casein kinase 1, epsilon | Xenopus laevis | Ampicillin | PMID:15539487 | Description: From John Graff, in Peters et al 1999. Notes for Use: Select clones with amp. Reference: used in Waxman JS, Hocking AM, Stoick CL, Moon RT. Zebrafish Dapper1 and Dapper2 play distinct roles in Wnt-mediated developmental processes. Development. 2004 Dec;131(23):5909-21. | Backbone Size:4095; Vector Backbone:pCS2+; Vector Types:Xenopus Expression; Bacterial Resistance:Ampicillin | K38R | 2026-08-15 01:09:42 | 0 |
|
XE90 pCS2P+ XCtBP Resource Report Resource Website |
RRID:Addgene_16704 | XCtBP | Xenopus laevis | Ampicillin | Plasmid History: Constructed by Jeff Brown. Notes for Use: The ~2 kb dropout of the Sal I digest of XTcf-3 interacting clone 2-1 (in pGBT9) was ligated into the XhoI site of pCS2P+. For CS2+MT XCtBP, the Sal I dropout was blunted with Klenow and cloned into the StuI site of pCS2+MT. | Backbone Size:4100; Vector Backbone:pCS2P+; Vector Types:Xenopus Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:09:41 | 0 | ||
|
XE51 XPKC-alpha Resource Report Resource Website |
RRID:Addgene_16746 | XPKC-Alpha | Xenopus laevis | Ampicillin | PMID:1547501 | SmaI linearize, SP6 for sense RNA. Notes for Use: Ref: used in Otte and Moon, Cell 68:1021-1029, 1992. | Backbone Marker:Promega; Backbone Size:2869; Vector Backbone:pGem2; Vector Types:Xenopus Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:09:44 | 0 | |
|
XE105 XPKC alpha-myc-CS2+ Resource Report Resource Website |
RRID:Addgene_16745 | XPKC-alpha-myc | Xenopus laevis | Ampicillin | PMID:10395542 | Insert: Xenopus PKC alpha with a c-myc epitope at carboxy terminus. For transcription cut with Not 1 and use SP6. Notes for Use: Ref: Sheldahl et al., Current Biology 9:695-698, 1999. | Backbone Size:4095; Vector Backbone:pCS2+; Vector Types:Xenopus Expression; Bacterial Resistance:Ampicillin | 2026-08-15 01:09:44 | 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.
Welcome to the PRECISE-TBI Resources search. From here you can search through a compilation of resources used by PRECISE-TBI and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that PRECISE-TBI 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 PRECISE-TBI then you can log in from here to get additional features in PRECISE-TBI 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 PRECISE-TBI 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.
