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Plasmid Name Proper Citation Insert Name Organism Bacterial Resistance Defining Citation Comments Vector Backbone Description Relevant Mutation Record Last Update Mentions Count
pXFokI-dCas9
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60901 Ampicillin PMID:27030102 The gRNA cloning strategy is exactly the same as for pX330/pX335. Backbone Size:9070; Vector Backbone:pUC ori vector; Vector Types:Mammalian Expression, CRISPR; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 1
pMTB-Multibow-mO
 
Resource Report
Resource Website
RRID:Addgene_60989 mKO Synthetic Ampicillin PMID:26010570 Multibow constructs contain repetitive loxP sites that make these constructs prone to recombination. The constructs display a few issues with bacterial stability and sequencing that need to be considered when amplifying, storing and using them. First, in our hands Multibow constructs have displayed instability in E.coli cultures and had low yield in Maxi/Midi-preps. Mini-prep is recommended to harvest Multibow constructs. For transformation, we have had success with 5-alpha F'Iq cells (NEB). Second, the sequencing of Multibow constructs may run into problems of low quality/inaccurate reads. A problematic trace file does not necessarily mean the construct is wrong or the sample has mixed sequences. Third, before using the constructs harvested from mini-prep for injections, we recommend a further purification step using DNA purification kits such as MinElute PCR purification kit (Qiagen). All Multibow constructs share a backbone of pMTB vector (AMP resistance) containing the tol2 sites for transgenic insertion and the loxP recombination sites. To validate the variable region, we recommend sequencing with this specific primer: 5'-CAGCAGGACCATTTATCATGCTGCTGC-3', which recognizes the end of the variable region. The Sp6 primer may not provide enough reading length to reach the variable region. Vector Backbone:pMTB; Vector Types:Zebrafish; Bacterial Resistance:Ampicillin 2026-08-15 01:17:38 0
pHR-scFv-GCN4-sfGFP-GB1-dWPRE
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_60907 scFv-GCN4 Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Vector Backbone:pHR; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 20
pHR-scFv-GCN4-sfGFP-GB1-NLS-dWPRE
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_60906 scFv-GCN4 Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Vector Backbone:pHR; Vector Types:Mammalian Expression, Lentiviral; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 34
pLV-sgCDKN1B#2 BFP
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60905 BFP Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Vector Backbone:pHR; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 1
pMTB-Multibow-G
 
Resource Report
Resource Website
RRID:Addgene_60980 EGFP Synthetic Ampicillin PMID:26010570 Multibow constructs contain repetitive loxP sites that make these constructs prone to recombination. The constructs display a few issues with bacterial stability and sequencing that need to be considered when amplifying, storing and using them. First, in our hands Multibow constructs have displayed instability in E.coli cultures and had low yield in Maxi/Midi-preps. Mini-prep is recommended to harvest Multibow constructs. For transformation, we have had success with 5-alpha F'Iq cells (NEB). Second, the sequencing of Multibow constructs may run into problems of low quality/inaccurate reads. A problematic trace file does not necessarily mean the construct is wrong or the sample has mixed sequences. Third, before using the constructs harvested from mini-prep for injections, we recommend a further purification step using DNA purification kits such as MinElute PCR purification kit (Qiagen). All Multibow constructs share a backbone of pMTB vector (AMP resistance) containing the tol2 sites for transgenic insertion and the loxP recombination sites. To validate the variable region, we recommend sequencing with this specific primer: 5'-CAGCAGGACCATTTATCATGCTGCTGC-3', which recognizes the end of the variable region. The Sp6 primer may not provide enough reading length to reach the variable region. Vector Backbone:pMTB; Vector Types:Zebrafish; Bacterial Resistance:Ampicillin 2026-08-15 01:17:38 0
CIP2Aprom204bp-pGL4.10Luc
 
Resource Report
Resource Website
RRID:Addgene_60874 204 bp promoter fragment of Cancerous Inhibitor of PP2A Homo sapiens Ampicillin PMID:21445343 Then various length luciferase promoter constructs were created using the Deletion Kit for Kilo-Sequencing (Takara Bio Inc., Japan) as per the manufacturer’s instructions. Please note that there are some discrepancies between Addgene's quality control sequences and the depositor's sequence. The depositor noted that these discrepancies do NOT affect plasmid function. Backbone Marker:Promega; Backbone Size:4242; Vector Backbone:pGL4.10(luc2); Vector Types:Luciferase, Promoterless; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 0
CIP2Aprom285bp-pGL4.10Luc
 
Resource Report
Resource Website
RRID:Addgene_60873 285 bp promoter fragment of Cancerous Inhibitor of PP2A2 Homo sapiens Ampicillin PMID:21445343 Then various length luciferase promoter constructs were created using the Deletion Kit for Kilo-Sequencing (Takara Bio Inc., Japan) as per the manufacturer’s instructions. Please note that there are some discrepancies between Addgene's quality control sequences and the depositor's sequence. The depositor noted that these discrepancies do NOT affect plasmid function. Backbone Marker:Promega; Backbone Size:4242; Vector Backbone:pGL4.10(luc2); Vector Types:Luciferase, Promoterless; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 0
pHRdSV40-NLS-dCas9-24xGCN4_v4-NLS-P2A-BFP-dWPRE
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_60910 dCas9 Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Vector Backbone:pHR; Vector Types:Mammalian Expression, Lentiviral, CRISPR; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 29
pcDNA4TO-mito-mCherry-10xGCN4_v4
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60914 mito-mCherry Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Vector Backbone:pcDNA4TO; Vector Types:; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 7
pcDNA4TO-mito-mCherry-24xGCN4_v1
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60913 mito-mCherry Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Vector Backbone:pcDNA4TO; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 4
GST-PBD H538A/K540M
 
Resource Report
Resource Website
RRID:Addgene_60879 Polo-like kinase 1 Homo sapiens Ampicillin PMID:23455152 Backbone Size:4969; Vector Backbone:pGEX-4T-2; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin H538A/K540M 2026-08-15 01:17:37 0
PGK-AAVS1ZFNL
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60916 AAVS1-ZFNL Ampicillin PMID:25630922 Vector Backbone:PUC18; Vector Types:; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 1
pcDNA4TO-K560-E236A-24xGCN4_v1-IRES-Puro
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60909 K560-E236A Ampicillin PMID:25307933 For more information, visit https://valelab4.ucsf.edu/external/research/suntag.html Backbone Marker:Invitrogen; Vector Backbone:pcDNA4TO; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:17:37 5
pMTB-Multibow-mfR
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_60991 mKate2 Synthetic Ampicillin PMID:26010570 Multibow constructs contain repetitive loxP sites that make these constructs prone to recombination. The constructs display a few issues with bacterial stability and sequencing that need to be considered when amplifying, storing and using them. First, in our hands Multibow constructs have displayed instability in E.coli cultures and had low yield in Maxi/Midi-preps. Mini-prep is recommended to harvest Multibow constructs. For transformation, we have had success with 5-alpha F'Iq cells (NEB). Second, the sequencing of Multibow constructs may run into problems of low quality/inaccurate reads. A problematic trace file does not necessarily mean the construct is wrong or the sample has mixed sequences. Third, before using the constructs harvested from mini-prep for injections, we recommend a further purification step using DNA purification kits such as MinElute PCR purification kit (Qiagen). All Multibow constructs share a backbone of pMTB vector (AMP resistance) containing the tol2 sites for transgenic insertion and the loxP recombination sites. To validate the variable region, we recommend sequencing with this specific primer: 5'-CAGCAGGACCATTTATCATGCTGCTGC-3', which recognizes the end of the variable region. The Sp6 primer may not provide enough reading length to reach the variable region. Vector Backbone:pMTB; Vector Types:Zebrafish; Bacterial Resistance:Ampicillin 2026-08-15 01:17:38 1
pMTB-Multibow-mR
 
Resource Report
Resource Website
RRID:Addgene_60990 dTomato Synthetic Ampicillin PMID:26010570 Multibow constructs contain repetitive loxP sites that make these constructs prone to recombination. The constructs display a few issues with bacterial stability and sequencing that need to be considered when amplifying, storing and using them. First, in our hands Multibow constructs have displayed instability in E.coli cultures and had low yield in Maxi/Midi-preps. Mini-prep is recommended to harvest Multibow constructs. For transformation, we have had success with 5-alpha F'Iq cells (NEB). Second, the sequencing of Multibow constructs may run into problems of low quality/inaccurate reads. A problematic trace file does not necessarily mean the construct is wrong or the sample has mixed sequences. Third, before using the constructs harvested from mini-prep for injections, we recommend a further purification step using DNA purification kits such as MinElute PCR purification kit (Qiagen). All Multibow constructs share a backbone of pMTB vector (AMP resistance) containing the tol2 sites for transgenic insertion and the loxP recombination sites. To validate the variable region, we recommend sequencing with this specific primer: 5'-CAGCAGGACCATTTATCATGCTGCTGC-3', which recognizes the end of the variable region. The Sp6 primer may not provide enough reading length to reach the variable region. Vector Backbone:pMTB; Vector Types:Zebrafish; Bacterial Resistance:Ampicillin 2026-08-15 01:17:38 0
DR274-eGFP sgRNA
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_61051 EGFP sgRNA Synthetic Kanamycin PMID:24179142 eGFP sgRNA = GGCGAGGGCGATGCCACCTA Backbone Marker:Joung Lab, Addgene plasmid # 42250; Vector Backbone:DR274; Vector Types:CRISPR; Bacterial Resistance:Kanamycin 2026-08-15 01:17:38 3
pCMU-TGNVHAr
 
Resource Report
Resource Website
RRID:Addgene_61178 AtVHA-a1 Spectinomycin PMID:25329881 Vector Backbone:pK7m34GW; Vector Types:Plant Expression; Bacterial Resistance:Spectinomycin 2026-08-15 01:17:39 0
pcDNA4TO-sfGFP-24xGCN4_v1
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_61056 sfGFP-24xGCN4_v1 peptide array Ampicillin PMID:25307933 For more information, visit http://valelab.ucsf.edu/external/research/suntag.html Vector Backbone:pcDNA4TO; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:17:38 1
pCMB-TGN41r
 
Resource Report
Resource Website
RRID:Addgene_61177 MtSYP41 Spectinomycin PMID:25329881 Vector Backbone:pK7m34GW; Vector Types:Plant Expression; Bacterial Resistance:Spectinomycin 2026-08-15 01:17:39 0

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