SPL11p::pCGTAG (SPL11p::NLS-GFP)
(Plasmid
#27411)
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 27411 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCGTAG
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Selectable markersHygromycin
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)Mach1
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Growth instructionsMACH-1 strain of E. coli (from Invitrogen)
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameSPL11 promoter
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SpeciesA. thaliana (mustard weed)
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MutationSPL11 promoter transcriptionally fused to a nuclear-localized GFP
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Entrez GeneAT1G27360 (a.k.a. F17L21.14, F17L21_14)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer M13 reverse (Common Sequencing Primers)
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
SPL11p::NLS-GFP was generated by PCR amplification of 2.2-kb genomic DNA. The resulting amplicon was then cloned into pCR8/GW-TOPO (Invitrogen) and recombined with pCGTAG.
The primers used to create this construct were 5'-AAATCTCGTCCAACT-3' and 5'-TCACGATATGGGTTG-3'.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
SPL11p::pCGTAG (SPL11p::NLS-GFP) was a gift from David Bartel (Addgene plasmid # 27411 ; http://n2t.net/addgene:27411 ; RRID:Addgene_27411) -
For your References section:
MicroRNAs prevent precocious gene expression and enable pattern formation during plant embryogenesis. Nodine MD, Bartel DP. Genes Dev. 2010 Dec 1. 24(23):2678-92. 10.1101/gad.1986710 PubMed 21123653