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pMLLCK-J72038
 
Resource Report
Resource Website 		RRID:Addgene_26183 Med21 aa1-132 for N-terminal tagging Saccharomyces cerevisiae Chloramphenicol and Kanamycin Note that this plasmid must be grown in both Chloramphenicol and Kanamycin Backbone Size:2646; Vector Backbone:pMLL-CK; Vector Types:Synthetic Biology, 2ab assembly vector; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:12:49 0
pCP5
 
Resource Report
Resource Website 		RRID:Addgene_35397 Chloramphenicol and Kanamycin PMID:21493687 Cloning nuclease targets into the BglII/SpeI sites of pCP5 removes the CcdB gene, thus allows negative selection against undigested backbone in common E. coli strains such as DH5-alpha. Backbone Marker:unknown; Backbone Size:13844; Vector Backbone:pDW1714; Vector Types:Yeast Expression, reporter; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:14:06 0
E pCMV-CFPLoxP-YFPatt
 
Resource Report
Resource Website 		RRID:Addgene_24509 ECFP, EYFP Vibrio fischeri Chloramphenicol and Kanamycin Note: This plasmid has been partially sequenced. Due to the presence of repeated features in the plasmid that prohibit thorough sequencing, the provided sequence should be considered theoretical and could contain errors. Please refer to Lu, Jian-Ping, Beatty, Laura, and Pinthus, Jehonathan . Dual expression recombinase based (DERB) single vector system for high throughput screening and verification of protein interactions in living cells. Available from Nature Precedings https://www.nature.com/articles/npre.2008.1550.2 Backbone Marker:Clontech; Backbone Size:6724; Vector Backbone:pCMV; Vector Types:Mammalian Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:12:33 0
Y pFe-YcLoxP-YnAtt
 
Resource Report
Resource Website 		RRID:Addgene_24510 Yn, Yc, ECFP, EYFP Aequorea victoria (Jellyfish) Chloramphenicol and Kanamycin Note: This plasmid has been partially sequenced. Due to the presence of repeated features in the plasmid that prohibit thorough sequencing, the provided sequence should be considered theoretical and could contain errors. Please refer to Lu, Jian-Ping, Beatty, Laura, and Pinthus, Jehonathan . Dual expression recombinase based (DERB) single vector system for high throughput screening and verification of protein interactions in living cells. Available from Nature Precedings (2008) http://precedings.nature.com/documents/1550/version/2 Backbone Marker:Invivogen; Backbone Size:7434; Vector Backbone:pVitro2; Vector Types:Mammalian Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:12:31 0
pDest-mCherry-N1
 
Resource Report
Resource Website
10+ mentions 		RRID:Addgene_31907 Chloramphenicol and Kanamycin PMID:20169111 Please note: the orientation of the MCS within this plasmid places mCherry on the c-terminus of your gene of interest. Backbone Marker:Clontech; Backbone Size:4722; Vector Backbone:pmcherry-N1; Vector Types:Mammalian Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:13:37 17
pMDC32-HPB
 
Resource Report
Resource Website
1+ mentions 		RRID:Addgene_32078 Chloramphenicol and Kanamycin PMID:19000159 Backbone Size:12096; Vector Backbone:pMDC32; Vector Types:Gateway destination binary vector; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:13:42 3
pMDC-pRPS2-HPB
 
Resource Report
Resource Website 		RRID:Addgene_32077 Chloramphenicol and Kanamycin PMID:19000159 Backbone Size:12767; Vector Backbone:pMDC32; Vector Types:Gateway destination binary vector; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:13:38 0
pJAK2.B
 
Resource Report
Resource Website 		RRID:Addgene_29463 Chloramphenicol and Kanamycin PMID:19647016 Replicative mycobacterial destination vector for recombination cloning. Please note that there are multiple discrepancies between Addgene's quality control sequence and the depositor's theoretical sequence. The Hmama lab assures us that these differences should not affect plasmid function. Backbone Size:4492; Vector Backbone:pMV261; Vector Types:Bacterial Expression, Mycobacteria expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:13:19 0
pJAK1.B
 
Resource Report
Resource Website 		RRID:Addgene_29462 Chloramphenicol and Kanamycin PMID:19647016 Integrative mycobacterial destination vector for recombination cloning. Please note that there are multiple discrepancies between Addgene's quality control sequence and the depositor's theoretical sequence. The Hmama lab assures us that these differences should not affect plasmid function. Backbone Size:4445; Vector Backbone:pMV361; Vector Types:Bacterial Expression, Mycobacteria expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:13:18 0
pcDNA3.2 GW delCMV
 
Resource Report
Resource Website
1+ mentions 		RRID:Addgene_29496 Chloramphenicol and Kanamycin PMID:21375737 Generic promoter-less destination vector Backbone Marker:Invitrogen; Backbone Size:7142; Vector Backbone:pcDNA3.2/V5-DEST; Vector Types:Mammalian Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:13:20 1
pDONR-221-P3-P5
 
Resource Report
Resource Website 		RRID:Addgene_186350 Chloramphenicol and Kanamycin PMID:17878951 Backbone was modified with ApaI (attP3) / EcoRI (attP5) and PstI (attP3) / EcoRV (attP5) sites Backbone Marker:PMID: 14736459; Backbone Size:4774; Vector Backbone:PDONR-221 P1-P2; Vector Types:Gateway Cloning; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:23:51 0
pDONR-221-P3-P4
 
Resource Report
Resource Website
1+ mentions 		RRID:Addgene_186351 Chloramphenicol and Kanamycin PMID:17878951 Backbone was modified with ApaI (attP3) / EcoRI (attP4) and PstI (attP3) / EcoRV (attP4) sites Backbone Marker:PMID: 14736459; Backbone Size:4768; Vector Backbone:PDONR-221 P1-P2; Vector Types:Gateway Cloning; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:23:49 2
pGL2_136
 
Resource Report
Resource Website 		RRID:Addgene_199083 Chloramphenicol and Kanamycin For standard propagation, supplement LB growth medium with 2% glucose (w/v) to repress sfYFP dropout expression, otherwise escape mutants may arise. Vector Backbone:n/a; Vector Types:Synthetic Biology; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:26:58 0
pKL2351
 
Resource Report
Resource Website
1+ mentions 		RRID:Addgene_199721 NPTII Synthetic Chloramphenicol and Kanamycin PMID:37070560 A 185T mutation was found in mCherry. Backbone Marker:Yiping Qi; Vector Backbone:pYPQ210; Vector Types:Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:27:04 1
Osa-pCAMBIA-1301-STTM5338
 
Resource Report
Resource Website 		RRID:Addgene_84236 miR5338 Rice Chloramphenicol and Kanamycin PMID:22345490 This plasmid used to disturb miR5338’s expression by STTM method invented by Dr. Guiliang Tang’s Lab in Michigan Technological University (Plant cell, 2012), Houghton, MI, USA. The method used to construct this plasmid refers to Tang et al., (Methods, 2012) with minor revision. The STTM sequence in this plasmid may contain discrepancies compared to the reference sequence(s). According to the depositing lab, these mutations should not affect plasmid function. For additional published information regarding this plasmid, please see https://www.cell.com/molecular-plant/pdf/S1674-2052(18)30275-2.pdf?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1674205218302752%3Fshowall%3Dtrue# Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:21:13 0
Osa-pCAMBIA-1301-STTM5144
 
Resource Report
Resource Website 		RRID:Addgene_84235 miR5144 Rice Chloramphenicol and Kanamycin PMID:22345490 This plasmid used to disturb miR5144’s expression by STTM method invented by Dr. Guiliang Tang’s Lab in Michigan Technological University (Plant cell, 2012), Houghton, MI, USA. The method used to construct this plasmid refers to Tang et al., (Methods, 2012) with minor revision. The STTM sequence in this plasmid may contain discrepancies compared to the reference sequence(s). According to the depositing lab, these mutations should not affect plasmid function. For additional published information regarding this plasmid, please see https://www.cell.com/molecular-plant/pdf/S1674-2052(18)30275-2.pdf?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1674205218302752%3Fshowall%3Dtrue# Backbone Marker:CAMBIA Company ; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:21:13 0
Osa-pCAMBIA-1301-STTM5794
 
Resource Report
Resource Website 		RRID:Addgene_84237 miR5794 Rice Chloramphenicol and Kanamycin PMID:22345490 This plasmid used to disturb miR5794’s expression by STTM method invented by Dr. Guiliang Tang’s Lab in Michigan Technological University (Plant cell, 2012), Houghton, MI, USA. The method used to construct this plasmid refers to Tang et al., (Methods, 2012) with minor revision. The STTM sequence in this plasmid may contain discrepancies compared to the reference sequence(s). According to the depositing lab, these mutations should not affect plasmid function. For additional published information regarding this plasmid, please see https://www.cell.com/molecular-plant/pdf/S1674-2052(18)30275-2.pdf?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1674205218302752%3Fshowall%3Dtrue# Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:21:17 0
Osa-pCAMBIA-1301-STTM169
 
Resource Report
Resource Website 		RRID:Addgene_84199 miR169 Rice Chloramphenicol and Kanamycin PMID:22345490 This plasmid used to disturb miR169’s expression by STTM method invented by Dr. Guiliang Tang’s Lab in Michigan Technological University (Plant cell, 2012), Houghton, MI, USA. The method used to construct this plasmid refers to Tang et al., (Methods, 2012) with minor revision. The STTM sequence in this plasmid may contain discrepancies compared to the reference sequence(s). According to the depositing lab, these mutations should not affect plasmid function. For additional published information regarding this plasmid, please see https://www.cell.com/molecular-plant/pdf/S1674-2052(18)30275-2.pdf?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1674205218302752%3Fshowall%3Dtrue# Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:21:12 0
Osa-pCAMBIA-1301-STTM167
 
Resource Report
Resource Website 		RRID:Addgene_84198 miR167 Rice Chloramphenicol and Kanamycin PMID:22345490 This plasmid used to disturb miR166’s expression by STTM method invented by Dr. Guiliang Tang’s Lab in Michigan Technological University (Plant cell, 2012), Houghton, MI, USA. The method used to construct this plasmid refers to Tang et al., (Methods, 2012) with minor revision The STTM sequence in this plasmid may contain discrepancies compared to the reference sequence(s). According to the depositing lab, these mutations should not affect plasmid function. For additional published information regarding this plasmid, please see https://www.cell.com/molecular-plant/pdf/S1674-2052(18)30275-2.pdf?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1674205218302752%3Fshowall%3Dtrue# Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:21:12 0
Osa-pCAMBIA-1301-STTM1430
 
Resource Report
Resource Website 		RRID:Addgene_84231 miR1430 Rice Chloramphenicol and Kanamycin PMID:22345490 This plasmid used to disturb miR1430’s expression by STTM method invented by Dr. Guiliang Tang’s Lab in Michigan Technological University (Plant cell, 2012), Houghton, MI, USA. The method used to construct this plasmid refers to Tang et al., (Methods, 2012) with minor revision The STTM sequence in this plasmid may contain discrepancies compared to the reference sequence(s). According to the depositing lab, these mutations should not affect plasmid function. For additional published information regarding this plasmid, please see https://www.cell.com/molecular-plant/pdf/S1674-2052(18)30275-2.pdf?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1674205218302752%3Fshowall%3Dtrue# Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin 2026-08-15 01:21:16 0

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