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http://www.addgene.org/84147

Species: Arabidopsis thaliana
Genetic Insert: STTM780.2
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
References:
Comments: The insert within this plasmid contains a 2x35S promoter, STTM, T35S and CmR.

Proper citation: RRID:Addgene_84147 Copy   

http://www.addgene.org/84140

Species: Arabidopsis thaliana
Genetic Insert: STTM771
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
References:
Comments: The insert within this plasmid contains a 2x35S promoter, STTM, T35S and CmR.

Proper citation: RRID:Addgene_84140 Copy   

http://www.addgene.org/84145

Species: Arabidopsis thaliana
Genetic Insert: STTM779.2
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
References:
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_84145 Copy   

http://www.addgene.org/84203

Species: Other
Genetic Insert: miR393
Vector Backbone Description: Backbone Marker:CAMBIA Company; Backbone Size:2846; Vector Backbone:pCAMBIA-1301; Vector Types:Bacterial Expression, Yeast Expression, Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
References:
Comments: This plasmid used to disturb miR393’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_84203 Copy   

http://www.addgene.org/84208

Species: Other
Genetic Insert: miR398
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
References:
Comments: This plasmid used to disturb miR398’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_84208 Copy   

http://www.addgene.org/84201

Species: Other
Genetic Insert: miR319
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
References:
Comments: This plasmid used to disturb miR319’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_84201 Copy   

http://www.addgene.org/84236

Species: Other
Genetic Insert: miR5338
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
References:
Comments: 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#

Proper citation: RRID:Addgene_84236 Copy   

http://www.addgene.org/84235

Species: Other
Genetic Insert: miR5144
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
References:
Comments: 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#

Proper citation: RRID:Addgene_84235 Copy   

http://www.addgene.org/84237

Species: Other
Genetic Insert: miR5794
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
References:
Comments: 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#

Proper citation: RRID:Addgene_84237 Copy   

http://www.addgene.org/84195

Species: Other
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
References:
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   

http://www.addgene.org/84196

Species: Other
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
References:
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   

http://www.addgene.org/84199

Species: Other
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
References:
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   

http://www.addgene.org/84198

Species: Other
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
References:
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   

http://www.addgene.org/84231

Species: Other
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
References:
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   

http://www.addgene.org/84234

Species: Other
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
References:
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   

http://www.addgene.org/84227

Species: Other
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
References:
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   

http://www.addgene.org/84226

Species: Other
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
References:
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   

http://www.addgene.org/84223

Species: Other
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
References:
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   

http://www.addgene.org/84222

Species: Other
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
References:
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   

    • RRID:Addgene_85752

http://www.addgene.org/85752

Species:
Genetic Insert:
Vector Backbone Description: Backbone Marker:Invitrogen ; Backbone Size:4762; Vector Backbone:pDONR 221; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
References:
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   

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