pRMH120
(Plasmid
#40593)
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PurposeExpresses Gal4BD-CRY2PHR and Gal4AD-CIB1 for light-inducible protein expression
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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 | 40593 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonep414TEF
- Backbone size w/o insert (bp) 5414
- Total vector size (bp) 10860
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Modifications to backboneGal4BD-CRY2PHR inserted at TEF MCS, pADH-Gal4AD-CIBFL-tADH inserted at KpnI site
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Vector typeYeast Expression
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Selectable markersTRP1
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 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 1
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Gene/Insert nameCRY2
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Alt namecryptochrome 2
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SpeciesA. thaliana (mustard weed)
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Insert Size (bp)1500
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Entrez GeneCRY2 (a.k.a. AT1G04400, AT-PHH1, ATCRY2, CRYPTOCHROME 2 APOPROTEIN, F19P19.14, F19P19_14, FHA, PHH1, cryptochrome 2)
- Promoter TEF
Cloning Information for Gene/Insert 1
- Cloning method Unknown
- 5′ sequencing primer n/a (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameCIB1
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SpeciesA. thaliana (mustard weed)
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Insert Size (bp)1000
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Entrez GeneCIB1 (a.k.a. AT4G34530, T4L20.110, T4L20_110, cryptochrome-interacting basic-helix-loop-helix 1)
- Promoter ADH1
Cloning Information for Gene/Insert 2
- Cloning method Unknown
- 5′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
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Article Citing this Plasmid
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.
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:
pRMH120 was a gift from Chandra Tucker (Addgene plasmid # 40593 ; http://n2t.net/addgene:40593 ; RRID:Addgene_40593) -
For your References section:
Light-mediated control of DNA transcription in yeast. Hughes RM, Bolger S, Tapadia H, Tucker CL. Methods. 2012 Aug 15. 10.1016/j.ymeth.2012.08.004 PubMed 22922268