pSPL10p::SPL10-GFP
(Plasmid
#27406)
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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 | 27406 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneKAN-GWR-GFP
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Vector typeused to create transgenic lines
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 nameSPL10
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SpeciesA. thaliana (mustard weed)
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Entrez GeneAT1G27370 (a.k.a. F17L21.15, F17L21_15)
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Tag
/ Fusion Protein
- GFP (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer n/a
- 3′ sequencing primer GFP 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
SPL10p::SPL10-GFP constructs were generated by cloning genomic fragments, including 1.7 kb upstream of and including the SPL10 coding sequence (CDS), into pENTR/D-TOPO (Invitrogen), and then recombining these plasmids with Gateway compatible pBIB-KAN-GWR-GFP plasmids using LR clonase (Invitrogen).
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:
pSPL10p::SPL10-GFP was a gift from David Bartel (Addgene plasmid # 27406 ; http://n2t.net/addgene:27406 ; RRID:Addgene_27406) -
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