Searching the RRID Resource Information Network
Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
Species: Rice
Genetic Insert: miR408-5p
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
Defining Citation: PMID:22345490
Comments: This plasmid used to disturb miR408-5p’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_84218 Copy
Species: Rice
Genetic Insert: miR408-3p
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 miR408-3p’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_84217 Copy
Species: Rice
Genetic Insert: miR390
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 miR390’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_84202 Copy
Species: Rice
Genetic Insert: miR395
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 miR395’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_84205 Copy
Species: Rice
Genetic Insert: miR394
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 miR394’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_84204 Copy
Species: Rice
Genetic Insert: miR397
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 miR397’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_84207 Copy
Species: Rice
Genetic Insert: miR396
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 miR396’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_84206 Copy
Species: Rice
Genetic Insert: miR171
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 miR171’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_84200 Copy
Species: Rice
Genetic Insert: miR166
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_84197 Copy
Species: Rice
Genetic Insert: miR1425
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 miR1425’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_84230 Copy
Species: Rice
Genetic Insert: miR1432
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 miR1432’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_84233 Copy
Species: Rice
Genetic Insert: miR529
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 miR529’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_84225 Copy
Species: Rice
Genetic Insert: miR528
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 miR528’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_84224 Copy
Species: Rice
Genetic Insert: miR827
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 miR827’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_84229 Copy
Species: Rice
Genetic Insert: miR820
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 miR820’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_84228 Copy
Vector Backbone Description: Backbone Marker:EMD Chemicals; Vector Backbone:pRARE; Vector Types:Bacterial Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:22267487
Proper citation: RRID:Addgene_84650 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: he BAC vector is derived from the E.coli F plasmid. The BAC vector was cloned into the high copy vector pK18, to increse 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 BAC vector seqeunces also carry the EGFP gene, under control of the HCMV MIEP, followed by SV40 polyA signal sequence. 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_85710 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_85753 Copy
Vector Backbone Description: Vector Backbone:pYPQ202; 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_86198 Copy
Vector Backbone Description: Vector Backbone:pMDC43; Vector Types:Plant Expression; Bacterial Resistance:Chloramphenicol and Kanamycin
Defining Citation: PMID:23056524
Comments: To enhance folding of the fusion proteins a flexible linker was introduced between the coding sequence of either fragment of YFP and the attR recombination site. For more information see: http://www.ibmcp.upv.es/FerrandoLabVectors/
Proper citation: RRID:Addgene_89488 Copy
Can't find your Plasmid?
We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific plasmid, it's easier to enter an RRID or an Addgene Catalog Number to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.
If you still could not find your plasmid in the search results, please help us by registering it into the system — it's easy. Register it with Addgene.
Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.
If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
You can save any searches you perform for quick access to later from here.
We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.
If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the sources that were queried against in your search that you can investigate further.
Here are the categories present within RRID that you can filter your data on
Here are the subcategories present within this category that you can filter your data on
If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.
