CFP_Rem_pcDNA4_HisMaxC
(Plasmid
#41651)
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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 | 41651 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA4/His-Max C
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Backbone manufacturerInvitrogen
- Total vector size (bp) 6853
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Vector typeMammalian Expression
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Selectable markersZeocin
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 numberUnknown
Gene/Insert
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Gene/Insert nameRem, GTP binding proteins (RGK)
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Alt nameRem1
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SpeciesM. musculus (mouse)
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Insert Size (bp)891
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GenBank IDNM_009047
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Entrez GeneRem1 (a.k.a. RP23-35I8.9, E030011C07Rik, Rem)
- Promoter CMV
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Tag
/ Fusion Protein
- CFP (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer T7_promoter
- 3′ sequencing primer BGH 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.
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:
CFP_Rem_pcDNA4_HisMaxC was a gift from Henry Colecraft (Addgene plasmid # 41651 ; http://n2t.net/addgene:41651 ; RRID:Addgene_41651) -
For your References section:
Distinct RGK GTPases differentially use alpha1- and auxiliary beta-binding-dependent mechanisms to inhibit CaV1.2/CaV2.2 channels. Yang T, Puckerin A, Colecraft HM. PLoS One. 2012;7(5):e37079. Epub 2012 May 10. 10.1371/journal.pone.0037079 PubMed 22590648