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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
mCherry-miniSOG-Keratin-17
 
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RRID:Addgene_55091 Keratin Homo sapiens Kanamycin PMID:21483721 . Excitation = 448 / 473; Emission = 500 / 528 Backbone Size:5500; Vector Backbone:mCherry-miniSOG; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin V282L 2026-08-15 01:16:46 0
mCherry-Talin-N-10
 
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1+ mentions
RRID:Addgene_55139 Talin Mus musculus Kanamycin PMID:22751201 . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 2
mCherry-SSTR3-N-17
 
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RRID:Addgene_55135 SSTR3 Mus musculus Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 0
mCherry-Smoothened1-N-18
 
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1+ mentions
RRID:Addgene_55134 Smoothened1 Mus musculus Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 2
mCherry-miniSOG-Vimentin-7
 
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RRID:Addgene_55099 NM_003380.3 Homo sapiens Kanamycin PMID:21483721 . Excitation = 448 / 473; Emission = 500 / 528 Backbone Size:5500; Vector Backbone:mCherry-miniSOG; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:46 0
mCherry-Sequestosome1-N-18
 
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1+ mentions
RRID:Addgene_55132 Sequestosome1 Homo sapiens Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 6
mCherry-TBRII-C-18
 
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RRID:Addgene_55141 TBRII Homo sapiens Kanamycin TBRII contains the H385N mutation . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin H385N 2026-08-15 01:16:47 0
mCherry-Talin-R-15
 
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RRID:Addgene_55140 Talin R Mus musculus Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin Talin Rod Domain 2026-08-15 01:16:47 0
mCherry-TOMM20-N-10
 
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10+ mentions
RRID:Addgene_55146 TOMM20 Homo sapiens Kanamycin Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 28
mCherry-TFR-20
 
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10+ mentions
RRID:Addgene_55144 TFR Homo sapiens Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 13
mCherry-Tensin1-C-14
 
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1+ mentions
RRID:Addgene_55143 Tensin1 Homo sapiens Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 1
mCherry-VASP-N-10
 
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RRID:Addgene_55153 VASP Mus musculus Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin A209T in VASP 2026-08-15 01:16:47 0
mCherry-UbiquitinC-N-18
 
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RRID:Addgene_55150 UbiquitinC Homo sapiens Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin aa 2-76 of NP_003324.1 2026-08-15 01:16:47 0
mCherry-WASH1-C-18
 
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1+ mentions
RRID:Addgene_55162 WASH1 Mus musculus Kanamycin WASH = WASH1. Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-C1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 1
mCherry-WASF2-N
 
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RRID:Addgene_55161 WASF2 Mus musculus Kanamycin . Excitation = 587; Emission = 610 Backbone Size:4750; Vector Backbone:mCherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Kanamycin 2026-08-15 01:16:47 0
pET StrepII-StrepII TEV LIC cloning vector (2RRT)
 
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1+ mentions
RRID:Addgene_55215 Ampicillin This plasmid is an empty vector. Your gene can be inserted with a LIC cloning protocol. All 2-series vectors work as single-expression vectors, as well as transfer vectors for our polycistronic system. The LIC cloning site is flanked by 5 pairs of restriction sites, so that your gene can easily be subcloned into our polycistronic destination vectors (2D, 2E, or 2Z). 2RRT has a TEV-cleavable N-terminal StrepII-StrepII tag. To clone into this vector, add LIC v1 tags to the 5' end of your PCR primers. Forward - 5'-TACTTCCAATCCAATGCA-3' Reverse - 5'-TTATCCACTTCCAATGTTATTA-3' Linearize the plasmid with SspI and gel purify. When digesting the DNA with T4 polymerase, use dCTP for insert and dGTP for vector. Vector Backbone:pET; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:16:48 1
His10-tag
 
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RRID:Addgene_55179 His10 Synthetic Chloramphenicol PMID:24295448 For sequencing of insert, use the following primers: fwd: TGCCACCTGACGTCTAAG rev: ATTACCGCCTTTGAGTGA Backbone Marker:iGEM; Backbone Size:2070; Vector Backbone:pSB1C3; Vector Types:Synthetic Biology, Bacillus BioBrick Box; Bacterial Resistance:Chloramphenicol 2026-08-15 01:16:47 0
pET His6 High pI protein 69 TEV LIC cloning vector (2-HpI-69)
 
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RRID:Addgene_55212 Ampicillin This plasmid is an empty vector. Your gene can be inserted with a LIC cloning protocol. All 2-series vectors work as single-expression vectors, as well as transfer vectors for our polycistronic system. The LIC cloning site is flanked by 5 pairs of restriction sites, so that your gene can easily be subcloned into our polycistronic destination vectors (2D, 2E, or 2Z). 2-HpI-69 has a TEV-cleavable N-terminal His6-High pI protein fusion tag. The high pI can improve solubility of your target protein. To clone into this vector, add LIC v1 tags to the 5' end of your PCR primers. Forward - 5'-TACTTCCAATCCAATGCA-3' Reverse - 5'-TTATCCACTTCCAATGTTATTA-3' Linearize the plasmid with SspI and gel purify. When digesting the DNA with T4 polymerase, use dCTP for insert and dGTP for vector. Vector Backbone:pET; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:16:48 0
pET His6 High pI protein 68 TEV LIC cloning vector (2-HpI-68)
 
Resource Report
Resource Website
1+ mentions
RRID:Addgene_55211 Ampicillin This plasmid is an empty vector. Your gene can be inserted with a LIC cloning protocol. All 2-series vectors work as single-expression vectors, as well as transfer vectors for our polycistronic system. The LIC cloning site is flanked by 5 pairs of restriction sites, so that your gene can easily be subcloned into our polycistronic destination vectors (2D, 2E, or 2Z). 2-HpI-68 has a TEV-cleavable N-terminal His6-High pI protein fusion tag. The high pI can improve solubility of your target protein.To clone into this vector, add LIC v1 tags to the 5' end of your PCR primers. Forward - 5'-TACTTCCAATCCAATGCA-3' Reverse - 5'-TTATCCACTTCCAATGTTATTA-3' Linearize the plasmid with SspI and gel purify. When digesting the DNA with T4 polymerase, use dCTP for insert and dGTP for vector. Vector Backbone:pET; Vector Types:Bacterial Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:16:48 1
pFastBac His6 TEV cloning vector with BioBrick PolyPromoter LIC Subcloning (438-B)
 
Resource Report
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10+ mentions
RRID:Addgene_55219 Ampicillin PMID:28668116 In order to increase the efficiency of subcloning with the Series-11 Macrobac plasmids we developed a new strategy the uses LIC (Ligation Independent Cloning). The problem with the Series-11 ligation mediated subcloning was that when the plasmid size approached or exceeded 20 kb we had to screen many colonies to find a positive. We developed a strategy to use LIC for subcloning. Because this method uses no ligase, the cloning background associated with re-ligation of the empty plasmid are eliminated. 438-B has a TEV cleavable His6 at the N-terminus. The 438-B vector use the LICv1 Forward and Reverse primers. LICv1Forward - 5'-TACTTCCAATCCAATGCA-3' LICv1 Reverse - 5'-TTATCCACTTCCAATGTTATTA-3' As the target plasmid size gets >20kb you may have to increase the amount of DNA you anneal and/or transform. We have found this method gives no background colonies at all and 100% of the colonies we pick are positive. The cells we transform into are XL1Blues with a competency ~6x10^7cfu/ul. For more information, please see our website: http://qb3.berkeley.edu/qb3/macrolab/ Vector Backbone:pFastBac; Vector Types:Insect Expression; Bacterial Resistance:Ampicillin 2026-08-15 01:16:48 14

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