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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
pCS2TAL3-DD
 
Resource Report
Resource Website
10+ mentions
RRID:Addgene_37275 Ampicillin PMID:22916025 For more information on Grunwald TALEN Add-On Plasmids please refer to: http://www.addgene.org/TALeffector/goldengate/add-ons/#grunwald Backbone Size:4168; Vector Backbone:pCS2; Vector Types:Mammalian Expression, Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 12
pTK21
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37396 Ran Homo sapiens Kanamycin PMID:22327364 Please note that Addgene's sequencing result exactly matches the full plasmid sequence provided by the depositing laboratory; however, when these sequences are compared to GenBank ID NP_006316.1 there appears to be a T24N mutation. Vector Backbone:pEGFP-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin T24N 2026-08-15 01:14:14 7
pCS2TAL3-RR
 
Resource Report
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10+ mentions
RRID:Addgene_37276 Ampicillin PMID:22916025 For more information on Grunwald TALEN Add-On Plasmids please refer to: http://www.addgene.org/TALeffector/goldengate/add-ons/#grunwald Backbone Size:4039; Vector Backbone:pCS2; Vector Types:Mammalian Expression, Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 11
CFP-GAI(1-532)
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37310 GAI Arabidopsis thaliana Kanamycin PMID:22446836 Backbone Marker:Clontech; Backbone Size:4700; Vector Backbone:pECFP-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin contains aa 1-532 2026-08-15 01:14:14 1
Lyn-CFP-GAI(1-92)
 
Resource Report
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1+ mentions
RRID:Addgene_37311 GAI Arabidopsis thaliana Kanamycin PMID:22446836 Lyn-CFP-FRB was created by inserting Lyn into the pEGFP- C1 vector (Clontech) whose EGFP is replaced with CFP-FRB. Vector Backbone:Lyn-CFP-FRB; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin contains aa 1-92 2026-08-15 01:14:14 1
10XSTAT92E–luciferase
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37393 SOCS36E enhancer fragment Drosophila melanogaster Ampicillin PMID:16055650 Perrimon Lab plasmid #446 A 441-bp genomic fragment in the enhancer of SOCS36E containing two potential STAT92E-binding sites was amplified by PCR, using five different sets of oligos: (1) CTGCAGGAACCACTCAGAGTGCCTGCGTGT (PstI), GAATTCATACAAAACTGTCTTAGGTGTTTA (EcoRI); (2) CTGCAGGAACCACTCAGAGTGCCTGCGTGT (PstI), CTGCAGATACAAAACTGTCTTAGGTGTTTA (PstI); (3) GAATTCGAACCACTCAGAGTGCCTGCGTGT (EcoRI), GAATTCATACAAAACTGTCTTAGGTGTTTA (EcoRI); (4) AGATCTGAACCACTCAGAGTGCCTGCGTGT (BglII), AGATCTATACAAAACTGTCTTAGGTGTTTA (BglII); (5) GCGGCCGCGAACCACTCAGAGTGCCTGCGTGT (NotI), GCGGCCGCATACAAAACTGTCTTAGGTGTTTA (NotI). Each amplified genomic fragment containing different restriction enzyme sites was sequentially subcloned into pUAST. The genomic fragment amplified using the first set of oligos was subcloned into the PstI/EcoRI sites of pUAST to generate 2XSTAT92E. The genomic fragment amplified using the second set of oligos was subcloned into the PstI site of 2XSTAT92E to generate 4XSTAT92E. The genomic fragment amplified using the third set of oligos was subcloned into the EcoRI site of 4XSTAT92E to generate 6XSTAT92E. The genomic fragment amplified using the fourth set of oligos was subcloned into the BglII site of 6XSTAT92E to generate 8XSTAT92E. Next, the hsp70 minimal promoter element was amplified from pUAST by PCR using oligos GCGGCCGCAGCGGAGACTCTAGCGAGCG (NotI) and CTCGAGAATTCCCTATTCAGAGTTCT (XhoI). This hsp70 minimal promoter was subcloned into the NotI/XhoI sites of 8XSTAT92E to generate 8XSTAT92E–hsp70. Again, the genomic fragment amplified using the fifth set of oligos was subcloned into the NotI site of 8XSTAT92E–hsp70 vector to generate 10XSTAT92E–hsp70. Finally, an XhoI/XbaI fragment containing the firefly luciferase gene from the pGL3–luciferase vector (Promega) was subcloned into the XhoI/XbaI sites of 10XSTAT92E–hsp70 to generate 10XSTAT92E–luciferase. Backbone Size:8904; Vector Backbone:pUAST; Vector Types:Insect Expression, Luciferase, JAK/STAT reporter construct; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 2
pCB163
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37388 Dynactin 2 Homo sapiens Ampicillin PMID:22327364 Please note that Addgene's sequencing results identified single nucleotide mismatches at bp# 2273 & 2347 when compared to the full plasmid sequence provided by the depositing laboratory. The mismatch at bp#2273 causes A7P mutation in the DCTN2 seqeuence. Vector Backbone:pBABE; Vector Types:Mammalian Expression, Retroviral; Bacterial Resistance:Ampicillin A7P 2026-08-15 01:14:14 2
pCaSpeR-4 porcupine (genomic DNA)
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37376 porcupine Drosophila melanogaster Ampicillin PMID:8985181 Perrimon Lab plasmid #123 The EcoRI-XbaI genomic DNA covering the porc locus was cloned in pCaspeR4 to generate a genomic porc rescue construct. Backbone Size:7855; Vector Backbone:pCaSpeR-4; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 1
pT7-EGFP-C1-HsNot1
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37370 HsNot1 Homo sapiens Kanamycin PMID:21981923 Backbone Marker:Clontech; Backbone Size:4755; Vector Backbone:pEGFP-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:14:14 1
Renilla luciferase-Pol III
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37380 PolIII-Renilla control reporter Drosophila melanogaster Ampicillin PMID:16311596 Perrimon Lab plasmid #414 The PolIII–Renilla luciferase control construct was generated by PCR amplification of a fragment (base pairs 43,224–43,389 of scaffold AE003823) of the promoter of the D. melanogaster RNA PolIII 128 subunit (RpIII128) with a 5' BglII and a 3' SpeI site and ligation of this fragment into the BglII and SpeI sites of pRL-null. Backbone Marker:Promega; Backbone Size:3320; Vector Backbone:pRL-null; Vector Types:Mammalian Expression, Luciferase; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 6
Cre Shine
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37404 Cre Shine Ampicillin Backbone Marker:Invitrogene; Backbone Size:5060; Vector Backbone:pcDNA3.1; Vector Types:Mammalian Expression, Cre/Lox; Bacterial Resistance:Ampicillin 2026-08-15 01:14:15 4
pTK24
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37406 Plk1 Homo sapiens Kanamycin PMID:22327364 Vector Backbone:pEGFP-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:14:15 1
pfast NPC1L1(NTD)
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37366 npc1l1 Homo sapiens Ampicillin PMID:21525977 There is a TEV cleavage site downstream of His tag. Backbone Marker:invitrogen; Backbone Size:5000; Vector Backbone:pFASTBAC; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin aa22-284only 2026-08-15 01:14:14 1
pQC NLS mCherry IX
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37354 NLS-mCherry Synthetic Ampicillin PMID:21397594 Backbone Marker:clontech; Backbone Size:6000; Vector Backbone:pQC; Vector Types:; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 5
pQC membrane TdTomato IX
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37351 membrane TdTomato Synthetic Ampicillin PMID:21397594 *palmitoylation sequence: 5'-atgctgtgctgtatgagaagaaccaaacaggttgaaaagaatgatgaggaccaaaagatc-3' Backbone Marker:clontech; Backbone Size:6000; Vector Backbone:pQC; Vector Types:; Bacterial Resistance:Ampicillin 2026-08-15 01:14:14 7
pBAD Strep His6 TEV LIC cloning vector (8HR)
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37505 Ampicillin This plasmid is an empty vector. Your gene can be inserted via LIC cloning. 8-series vectors are induced with L-arabinose for tighter control of expression. Glucose can be added to the medium to further inhibit leaky expression. The plasmid can be expressed in any E. coli line that lacks proteases. 8HR adds a TEV-cleavable His6 and a strep tag to the N terminus of your protein. The dual affinity tags can help to purify difficult proteins. To clone into this vector, add LIC v1 tags to the 5' end of your PCR primers. Forward - 5'TACTTCCAATCCAATGCA3' Reverse - 5'TTATCCACTTCCAATGTTATTA3' Linearize the plasmid with SspI and gel purify. When digesting the DNA with T4 polymerase, use dCTP for insert and dGTP for vector. Visit http://qb3.berkeley.edu/qb3/macrolab/ for more information on this vector can be found through Backbone Size:5729; Vector Backbone:pBAD; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:15 1
pPD95.75-wVenus
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37464 Ampicillin PMID:22022276 Backbone Marker:Andrew Fire (Addgene plasmid # 1494); Vector Backbone:pPD95.75; Vector Types:Worm Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:15 2
myc-NLRC5
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37509 NLRC5 Homo sapiens Ampicillin PMID:22490867 Backbone Marker:Invitrogen; Backbone Size:5446; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:15 5
pAAV-EF1a-DIO-HB
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37452 Histone, 2A element, rabies B19 glycoprotein Ampicillin Please note that there are 2 mutations in Histone, D26G and V119I. These mutations should not affect plasmid function. Vector Backbone:AAV; Vector Types:AAV; Bacterial Resistance:Ampicillin 2026-08-15 01:14:15 4
p6897 PHAGE-P CMVT N-HA-hE6AP III wt
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_37605 E6AP III Homo sapiens Ampicillin PMID:22645313 Backbone Size:7800; Vector Backbone:PHAGE-P CMVt N-HA GAW; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:14:15 2

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