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Species: Rice
Genetic Insert: miR159
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR159’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#
Proper citation: RRID:Addgene_84195 Copy
Species: Rice
Genetic Insert: miR164
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR164’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#
Proper citation: RRID:Addgene_84196 Copy
Species: Rice
Genetic Insert: miR169
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: 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#
Proper citation: RRID:Addgene_84199 Copy
Species: Rice
Genetic Insert: miR167
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: 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#
Proper citation: RRID:Addgene_84198 Copy
Species: Rice
Genetic Insert: miR1430
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: 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#
Proper citation: RRID:Addgene_84231 Copy
Species: Rice
Genetic Insert: miR1861
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR1861’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#
Proper citation: RRID:Addgene_84234 Copy
Species: Rice
Genetic Insert: miR535
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR535’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#
Proper citation: RRID:Addgene_84227 Copy
Species: Rice
Genetic Insert: miR530-3p
Vector Backbone Description: Backbone Marker:CAMBIA Company ; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR530-3p’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#
Proper citation: RRID:Addgene_84226 Copy
Species: Arabidopsis thaliana
Genetic Insert: STTM863-3p
Vector Backbone Description: Backbone Marker:Guiliang Tang (Addgene plasmid # 44182); Backbone Size:8608; Vector Backbone:pFGC5941-PacI; Vector Types:Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:23098881
Comments: The insert within this plasmid contains a 2x35S promoter, STTM, T35S and CmR.
Proper citation: RRID:Addgene_84182 Copy
Species: Arabidopsis thaliana
Genetic Insert: STTM862-3p
Vector Backbone Description: Backbone Marker:Guiliang Tang (Addgene plasmid # 44182); Backbone Size:8608; Vector Backbone:pFGC5941-PacI; Vector Types:Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:23098881
Comments: The insert within this plasmid contains a 2x35S promoter, STTM, T35S and CmR. The STTM sequence in the plasmid contains discrepancies compared to the reference sequence. According to the depositing lab, these mutations should not affect plasmid function.
Proper citation: RRID:Addgene_84181 Copy
Species: Rice
Genetic Insert: miR444
Vector Backbone Description: Backbone Marker:CAMBIA Company ; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR444’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#
Proper citation: RRID:Addgene_84223 Copy
Species: Arabidopsis thaliana
Genetic Insert: STTM868-3p
Vector Backbone Description: Backbone Marker:Guiliang Tang (Addgene plasmid # 44182); Backbone Size:8608; Vector Backbone:pFGC5941-PacI; Vector Types:Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:23098881
Comments: The insert within this plasmid contains a 2x35S promoter, STTM, T35S and CmR.
Proper citation: RRID:Addgene_84189 Copy
Species: Rice
Genetic Insert: miR439
Vector Backbone Description: Backbone Marker:CAMBIA Company ; Backbone Size:11827; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR439’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#
Proper citation: RRID:Addgene_84222 Copy
Vector Backbone Description: Vector Backbone:pK18; Vector Types:Bacterial Expression, Cre/Lox, Herpesvirus Cloning; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:10888635
Comments: The BAC vector is derived from the E.coli F plasmid. The BAC vector was cloned into the high copy vector pK18, to increase yields. The BAC vector is typically excised by PacI. The BAC vector contains genes for participation (sopA, B,C, a repE gene (required for replication) and an origin of replication (oriS). There is also a chloramphenicol resistance gene. The BAC vector carries a gpt gene, driven by the HSV tk promoter; the gpt gene is followed by the SV40 polyA signal sequence (ca 125 bp). The BAC vector is terminally flanked by loxP sites. The plasmid contains also a 1.5 kb EcoRI-fragment from the murine herpesvirus MHV68. The sequence of pK18 is available from Genbank ACCESSION M17626.
Proper citation: RRID:Addgene_85709 Copy
Vector Backbone Description: Backbone Marker:Invitrogen ; Backbone Size:4762; Vector Backbone:pDONR 221; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:28017692
Comments: Please note that there are some seqeunce discrepancies between Addgene's quality control sequences and the depositor's genbank file. The depositor noted that these discrepancies do NOT affect plasmid function.
Proper citation: RRID:Addgene_85752 Copy
Vector Backbone Description: Vector Backbone:pMDC32; Vector Types:Plant Expression, Gateway compatible attR1-attR2 destination vector; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:28211909
Comments: Note: Addgene's quality control sequencing finds a 1.2kb transposable element upstream of the Kanamycin resistance cassette. This inserted sequence does not affect plasmid function.
Proper citation: RRID:Addgene_86207 Copy
Vector Backbone Description: Vector Backbone:pSC218; Vector Types:Plant Expression, CRISPR; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:29087011
Comments: 112-31:9.1. Alternative name of plasmid: pSG218RG.
Proper citation: RRID:Addgene_104780 Copy
Vector Backbone Description: Vector Backbone:pENTR/D derivative; Vector Types:Synthetic Biology; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:29847550
Proper citation: RRID:Addgene_105337 Copy
Vector Backbone Description: Vector Backbone:pJOG397 (pENTR/D derivative); Vector Types:Synthetic Biology; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:29847550
Comments: Please note the orientation of the elements inside the Gateway cassettes are flipped. The depositing lab has noted that this orientation will not affect plasmid function.
Proper citation: RRID:Addgene_105340 Copy
Vector Backbone Description: Vector Backbone:pMEXC3H; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:29934571
Proper citation: RRID:Addgene_110080 Copy
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