pSB65 - pL0_tGFP-I (CDS1)
(Plasmid
#123182)
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PurposeGolden Gate (MoClo; CDS1) compatible turbo GFP gene from P. plumata with an intron for transient and stable expression in plants (moved to a CDS1 position from pICSL50016; Engler et al., 2014)
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Depositing Labs
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 123182 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepICH41308
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Backbone manufacturerWeber et al., 2011 (DOI:10.1371/journal.pone.0016765)
- Backbone size w/o insert (bp) 2247
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Vector typePlant Expression ; part for plant expression
Growth in Bacteria
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Bacterial Resistance(s)Spectinomycin and Streptomycin, 50 & 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameturboGFP codon-optimised for plants (P. plumata) with intron, U5 small nuclear ribonucleoprotein component (A. thaliana)
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SpeciesSynthetic
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Insert Size (bp)907
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MutationNo BpiI and BsaI sites; codon-optimised for plants
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Unknown (unknown if destroyed)
- 3′ cloning site Unknown (unknown if destroyed)
Resource Information
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Supplemental Documents
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
Golden Gate (MoClo - Weber et al., 2011), CDS1 position, turboGFP (P. plumata) codon-optimised for plants with intron, U5 small nuclear ribonucleoprotein component (A. thaliana) for transient and stable expression in plants. (Moved to CDS1 position from pICSL50016; Engler et al., 2014)
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:
pSB65 - pL0_tGFP-I (CDS1) was a gift from Erin Cram & Carolyn Lee-Parsons (Addgene plasmid # 123182 ; http://n2t.net/addgene:123182 ; RRID:Addgene_123182) -
For your References section:
EASI Transformation: An Efficient Transient Expression Method for Analyzing Gene Function in Catharanthus roseus Seedlings. Mortensen S, Bernal-Franco D, Cole LF, Sathitloetsakun S, Cram EJ, Lee-Parsons CWT. Front Plant Sci. 2019 Jun 11;10:755. doi: 10.3389/fpls.2019.00755. eCollection 2019. 10.3389/fpls.2019.00755 PubMed 31263474