Searching across hundreds of databases
Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
Species: Drosophila melanogaster
Genetic Insert: Nibbler
Vector Backbone Description: Vector Backbone:pAFMW; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_188598 Copy
Species: Drosophila melanogaster
Genetic Insert: dSarm isoform E
Vector Backbone Description: Backbone Size:9000; Vector Backbone:pCASPR (attB); Vector Types:; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_187870 Copy
Species: Drosophila melanogaster
Genetic Insert: CG8333
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:2536; Vector Backbone:pDONR221; Vector Types:Other, Gateway Donor Vector; Bacterial Resistance:Kanamycin
References:
Comments: Please note that the ORFs in this collection were cloned open-ended (without a stop codon).
Proper citation: RRID:Addgene_34188 Copy
Species: Drosophila melanogaster
Genetic Insert: Polycomb
Vector Backbone Description: Backbone Size:5680; Vector Backbone:pET-11d; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_183781 Copy
Species: Drosophila melanogaster
Genetic Insert: mini-white
Vector Backbone Description: Backbone Size:4300; Vector Backbone:pUAST; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
References:
Comments: pUASTP2.1 contains a P-element target for RMCE, the mini-white gene flanked by inverted attP sites. It is a derivative of PUASTP2 in which the UAS and TATA sequences flanking the cassette have been removed. (Specifically, PUASTP2 was digested with BamHI and StuI to remove UAS-TATA-attP, and an attP-containing BamHI-EcoRV fragment from pTA-attP was inserted). This vector can be used to generate target lines by standard P element transgenesis.
Proper citation: RRID:Addgene_13842 Copy
Species: Drosophila melanogaster
Genetic Insert: mini-white
Vector Backbone Description: Backbone Size:5500; Vector Backbone:pUAST; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
References:
Comments: pUASTP2 contains a P-element target for RMCE, the mini-white gene flanked by inverted attP sites. This target cassette was contructed in the parent vector pUAST. This vector can be used to generate target lines by standard P element transgenesis.
Please note that the UAS binding sites and hsp70 promoter of pUAST are outside of the exchange cassette in this vector - i.e. following RMCE, these elements will remain flanking the cassette.
Proper citation: RRID:Addgene_13843 Copy
Species: Drosophila melanogaster
Genetic Insert: Asunder
Vector Backbone Description: Vector Backbone:CS2; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_47041 Copy
Species: Drosophila melanogaster
Genetic Insert: Drosophila Rae1
Vector Backbone Description: Backbone Size:2563; Vector Backbone:pDONR221; Vector Types:Insect Expression; Bacterial Resistance:Kanamycin
References:
Comments:
Proper citation: RRID:Addgene_124240 Copy
Species: Drosophila melanogaster
Genetic Insert: U6:3-gRNA
Vector Backbone Description: Backbone Marker:Fillip Port; Vector Backbone:pCFD3-dU6-3gRNA (Addgene 49410); Vector Types:Insect Expression, CRISPR; Bacterial Resistance:Ampicillin
References:
Comments: When describing the use of this plasmid in publications, please state that it is derived from pCFD3 and cite:
Port et al. Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila. Proc Natl Acad Sci U S A. 2014 Jul 22;111(29):E2967-76. doi: 10.1073/pnas.1405500111
In pCFD3.1, the BbsI sites have been mutated in mini-white, which allows use of the remaining BbsI sites for gRNA cloning (using the protocol for pCFD3 (https://www.crisprflydesign.org/plasmids/)).
Proper citation: RRID:Addgene_123366 Copy
Species: Drosophila melanogaster
Genetic Insert: Kinesin 1-401 iLid His tag
Vector Backbone Description: Backbone Size:2500; Vector Backbone:pT7-7; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_122484 Copy
Species: Drosophila melanogaster
Genetic Insert: Or47a
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:5427; Vector Backbone:pcDNA3.1(-); Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
References:
Comments: Please visit https://www.biorxiv.org/content/10.1101/669127v1 for BioRxiv preprint
Proper citation: RRID:Addgene_126472 Copy
Species: Drosophila melanogaster
Genetic Insert: Or47a
Vector Backbone Description: Backbone Marker:Invitrogen; Backbone Size:5427; Vector Backbone:pcDNA3.1(-); Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
References:
Comments: Please visit https://www.biorxiv.org/content/10.1101/669127v1 for BioRxiv preprint
Proper citation: RRID:Addgene_126473 Copy
Species: Drosophila melanogaster
Genetic Insert: DmelOrco
Vector Backbone Description: Backbone Size:4111; Vector Backbone:pCMV-BI; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
References:
Comments: Is it recommended to digest the vector with XhoI and PvuI-HF and gel purify the two bands before sequencing as the two CMV promoters and SV40-polyA sequences are very similar to each other. Use the EcoRI restriction site for best functional expression on the MCS2. Please visit https://www.biorxiv.org/content/10.1101/669127v1 for BioRxiv preprint
Proper citation: RRID:Addgene_126476 Copy
Species: Drosophila melanogaster
Genetic Insert: Or47a
Vector Backbone Description: Backbone Size:4111; Vector Backbone:pCMV-BI; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
References:
Comments: Is it recommended to digest the vector with XhoI and NaeI and gel purify the two bands before sequencing as the two CMV promoters and SV40-polyA sequences are very similar to each other Please visit https://www.biorxiv.org/content/10.1101/669127v1 for BioRxiv preprint
Proper citation: RRID:Addgene_126478 Copy
Species: Drosophila melanogaster
Genetic Insert: Or56a
Vector Backbone Description: Backbone Size:4111; Vector Backbone:pCMV-BI; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin
References:
Comments: Is it recommended to digest the vector with XhoI and NaeI and gel purify the two bands before sequencing as the two CMV promoters and SV40-polyA sequences are very similar to each other Please visit https://www.biorxiv.org/content/10.1101/669127v1 for BioRxiv preprint
Proper citation: RRID:Addgene_126479 Copy
Species: Drosophila melanogaster
Genetic Insert: 2.4kb mhc enhancer element
Vector Backbone Description: Backbone Marker:Tudor A. Fulga; Backbone Size:11291; Vector Backbone:pJC-20xUAS-TALE3-VP64-P10; Vector Types:Insect Expression, TALEN; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_104611 Copy
Species: Drosophila melanogaster
Genetic Insert: 0.8kb ase enhancer element
Vector Backbone Description: Backbone Marker:Tudor A. Fulga; Backbone Size:11305; Vector Backbone:pJC-20xUAS-TALE3-VP64-P10; Vector Types:Insect Expression, TALEN; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_104610 Copy
Species: Drosophila melanogaster
Genetic Insert: 1.9kb repo enhancer element
Vector Backbone Description: Backbone Marker:Tudor A. Fulga; Backbone Size:11333; Vector Backbone:pJC-20xUAS-TALE4-VP64-P10; Vector Types:Insect Expression, TALEN; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_104612 Copy
Species: Drosophila melanogaster
Genetic Insert: Drosophila melanogaster PRL
Vector Backbone Description: Backbone Marker:Novagen Inc., Madison, WI; Backbone Size:5708; Vector Backbone:pET-15B; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_166418 Copy
Species: Drosophila melanogaster
Genetic Insert: dAtg1
Vector Backbone Description: Vector Backbone:pUAST; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin
References:
Comments:
Proper citation: RRID:Addgene_111801 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 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:
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 RRID 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 RRID 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.
