Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Plasmids are provided by Addgene and DGRC.

Search

Type in a keyword to search

On page 59 showing 1161 ~ 1180 out of 4,486 results
Snippet view Table view Download Top 1000 Results
Click the to add this resource to a Collection

http://www.addgene.org/195608

Species: Saccharomyces cerevisiae
Genetic Insert: PI-SceI
Vector Backbone Description: Backbone Marker:Novagen; Vector Backbone:pET-23a; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:7890714
Comments: Expresses the excised intein of the VMA1 gene product including amino-terminal methionine-cysteine residues. Contains silent AvrII and RsrII sites near the borders of the N-terminal LAGLIDADG motif and silent EaeI and SnaBI sites near the borders of the C-terminal motif. Contains a D218A mutation in the first LAGLIDADG motif that inactivates the protein.

Proper citation: RRID:Addgene_195608 Copy   


http://www.addgene.org/195609

Species: Saccharomyces cerevisiae
Genetic Insert: PI-SceI
Vector Backbone Description: Vector Backbone:pT7-7; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:7890714
Comments: Expresses the excised intein of the VMA1 gene product including amino-terminal methionine-cysteine residues. Contains silent AvrII and RsrII sites near the borders of the N-terminal LAGLIDADG motif and silent EaeI and SnaBI sites near the borders of the C-terminal motif. Contains a D326A mutation in the second LAGLIDADG motif that inactivates the protein.

Proper citation: RRID:Addgene_195609 Copy   


  • RRID:Addgene_184769

http://www.addgene.org/184769

Species: Saccharomyces cerevisiae
Genetic Insert: ACH1
Vector Backbone Description: Vector Backbone:UG72-2GFP; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:32859196

Proper citation: RRID:Addgene_184769 Copy   


  • RRID:Addgene_184764

http://www.addgene.org/184764

Species: Saccharomyces cerevisiae
Genetic Insert: SEC7
Vector Backbone Description: Vector Backbone:UG74-2GFP; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:32859196

Proper citation: RRID:Addgene_184764 Copy   


  • RRID:Addgene_184771

http://www.addgene.org/184771

Species: Saccharomyces cerevisiae
Genetic Insert: SYS1
Vector Backbone Description: Vector Backbone:UG72-2GFP; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:32859196

Proper citation: RRID:Addgene_184771 Copy   


http://www.addgene.org/184775

Species: Saccharomyces cerevisiae
Genetic Insert: proGAL-Aur1
Vector Backbone Description: Vector Backbone:GAL-UG75; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:32859196

Proper citation: RRID:Addgene_184775 Copy   


  • RRID:Addgene_160385

http://www.addgene.org/160385

Species: Saccharomyces cerevisiae
Genetic Insert: mak10 gRNA
Vector Backbone Description: Backbone Marker:Addgene $ 60847; Backbone Size:8761; Vector Backbone:pCAS; Vector Types:Yeast Expression; Bacterial Resistance:Kanamycin

Proper citation: RRID:Addgene_160385 Copy   


  • RRID:Addgene_195038

http://www.addgene.org/195038

Species: Saccharomyces cerevisiae
Genetic Insert: KanR
Vector Backbone Description: Backbone Size:2400; Vector Backbone:pFA6a; Vector Types:yeast genomic targeting; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36503721
Comments: This plasmid can be used in place of the original pFA6a series to introduce targeted mutation by selectable marker insertion in yeast while preventing off-target disruption of insertion neighboring genes caused by cassette promoter driven transcription interference. For more information regarding these plasmids see our article (Powers et al., eLife 2022) "Bidirectional promoter activity from expression cassettes can drive off-target repression of neighboring gene translation" The backbone and KanMX cassette was amplified from pFA6a-kanMX6 (Longtine et al., 1998), the tDEG1 sequence was amplified from S. cerevisiae gDNA.

Proper citation: RRID:Addgene_195038 Copy   


  • RRID:Addgene_195040

http://www.addgene.org/195040

Species: Saccharomyces cerevisiae
Genetic Insert: His5+
Vector Backbone Description: Backbone Size:2458; Vector Backbone:pFA6a; Vector Types:yeast genomic targeting; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36503721
Comments: This plasmid can be used in place of the original pFA6a series to introduce targeted mutation by selectable marker insertion in yeast while preventing off-target disruption of insertion neighboring genes caused by cassette promoter driven transcription interference. For more information regarding these plasmids see our article (Powers et al., eLife 2022) "Bidirectional promoter activity from expression cassettes can drive off-target repression of neighboring gene translation" The backbone and KanMX cassette was amplified from pFA6a-kanMX6 (Longtine et al., 1998), the tDEG1 and tCYC1 sequences were amplified from S. cerevisiae gDNA.

Proper citation: RRID:Addgene_195040 Copy   


  • RRID:Addgene_195042

http://www.addgene.org/195042

Species: Saccharomyces cerevisiae
Genetic Insert: NatR
Vector Backbone Description: Backbone Size:2458; Vector Backbone:pFA6a; Vector Types:yeast genomic targeting; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36503721
Comments: This plasmid can be used in place of the original pFA6a series to introduce targeted mutation by selectable marker insertion in yeast while preventing off-target disruption of insertion neighboring genes caused by cassette promoter driven transcription interference. For more information regarding these plasmids see our article (Powers et al., eLife 2022) "Bidirectional promoter activity from expression cassettes can drive off-target repression of neighboring gene translation" The backbone and KanMX cassette was amplified from pFA6a-kanMX6 (Longtine et al., 1998), the tDEG1 and tCYC1 sequences were amplified from S. cerevisiae gDNA.

Proper citation: RRID:Addgene_195042 Copy   


  • RRID:Addgene_195044

http://www.addgene.org/195044

Species: Saccharomyces cerevisiae
Genetic Insert: NatR
Vector Backbone Description: Backbone Size:2400; Vector Backbone:pFA6a; Vector Types:yeast genomic targeting; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36503721
Comments: This plasmid can be used in place of the original pFA6a series to introduce targeted mutation by selectable marker insertion in yeast while preventing off-target disruption of insertion neighboring genes caused by cassette promoter driven transcription interference. For more information regarding these plasmids see our article (Powers et al., eLife 2022) "Bidirectional promoter activity from expression cassettes can drive off-target repression of neighboring gene translation" The backbone was amplified from pFA6a-kanMX6 (Longtine et al., 1998), the NatR gene and C. glabrata PGK1 promoter and terminator were synthesized on a gene block from IDT, the tCYC1 sequence was amplified from S. cerevisiae gDNA.

Proper citation: RRID:Addgene_195044 Copy   


http://www.addgene.org/194519

Species: Saccharomyces cerevisiae
Genetic Insert: TIF4631 leader sequence
Vector Backbone Description: Backbone Marker:Academic publication; Backbone Size:6018; Vector Backbone:pRS315; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36481666

Proper citation: RRID:Addgene_194519 Copy   


  • RRID:Addgene_196615

http://www.addgene.org/196615

Species: Saccharomyces cerevisiae
Genetic Insert: UGP1::mCherry-AID(71-114)-NatMX
Vector Backbone Description: Backbone Marker:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC55758/; Backbone Size:2531; Vector Backbone:pG23A, originally HO-poly-KanMX4-HO; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36849832
Comments: Cloning details are provided in Supplementary Table 2 of the paper. Details of the parent plasmid pG23A can be found on Addgene (Plasmid #102884).

Proper citation: RRID:Addgene_196615 Copy   


  • RRID:Addgene_196614

http://www.addgene.org/196614

Species: Saccharomyces cerevisiae
Genetic Insert: ATP3::mCherry-AID(71-114)-NatMX
Vector Backbone Description: Backbone Marker:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC55758/; Backbone Size:2531; Vector Backbone:pG23A, originally HO-poly-KanMX4-HO; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36849832
Comments: Cloning details are provided in Supplementary Table 2 of the paper. Details of the parent plasmid pG23A can be found on Addgene (Plasmid #102884).

Proper citation: RRID:Addgene_196614 Copy   


  • RRID:Addgene_196613

http://www.addgene.org/196613

Species: Saccharomyces cerevisiae
Genetic Insert: S000001911
Vector Backbone Description: Vector Backbone:pROS13; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36849832
Comments: Cloning details are in the Methods section and Supplementary Table 2 of the paper.

Proper citation: RRID:Addgene_196613 Copy   


http://www.addgene.org/196835

Species: Saccharomyces cerevisiae
Genetic Insert: Pab1
Vector Backbone Description: Backbone Size:7167; Vector Backbone:pOBD2; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:25671604
Comments: pOBD2 + NcoI-PAB1(369-612 bp)-SalI. Expresses Pab1 RRM2 fragment with E181R mutation. Expresses Pab1 fragment fused to GAL4BD.

Proper citation: RRID:Addgene_196835 Copy   


  • RRID:Addgene_196833

http://www.addgene.org/196833

Species: Saccharomyces cerevisiae
Genetic Insert: eIF4G1
Vector Backbone Description: Backbone Size:8429; Vector Backbone:pOAD; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:25671604
Comments: pOAD + EcoRI-eIF4G1(1-1023)-SalI. (W303 strain as a genomic template). Expresses eIF4G1 N' terminus fused to GAL4AD

Proper citation: RRID:Addgene_196833 Copy   


  • RRID:Addgene_197047

http://www.addgene.org/197047

Species: Saccharomyces cerevisiae
Genetic Insert: MCP-2xGFP
Vector Backbone Description: Vector Backbone:pRS305; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36357695

Proper citation: RRID:Addgene_197047 Copy   


  • RRID:Addgene_196616

http://www.addgene.org/196616

Species: Saccharomyces cerevisiae
Genetic Insert: Superfolder GFP
Vector Backbone Description: Backbone Marker:ATCC; Backbone Size:4573; Vector Backbone:HO-poly-KanMX4-HO (ATCC 87804); Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:36849832
Comments: Supplementary Table 2 of the paper provides details on the cloning of the plasmid.

Proper citation: RRID:Addgene_196616 Copy   


  • RRID:Addgene_198597

http://www.addgene.org/198597

Species: Saccharomyces cerevisiae
Genetic Insert: PAH1
Vector Backbone Description: Vector Backbone:UG75; Vector Types:Yeast Expression; Bacterial Resistance:Ampicillin
Defining Citation: PMID:32859196

Proper citation: RRID:Addgene_198597 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.

Can't find the RRID you're searching for? X
  1. RRID Portal Resources

    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.

  2. Navigation

    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.

  3. Logging in and Registering

    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.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Save Your Search

    You can save any searches you perform for quick access to later from here.

  6. Query Expansion

    We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.

  7. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  8. Sources

    Here are the sources that were queried against in your search that you can investigate further.

  9. Categories

    Here are the categories present within RRID that you can filter your data on

  10. Subcategories

    Here are the subcategories present within this category that you can filter your data on

  11. Further Questions

    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.

X