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PurposeVisualization of Dendritic Golgi Satellite
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 73297 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepmCherryN1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4773
- Total vector size (bp) 4896
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Modifications to backboneThis plasmid contains the multiple cloning site (MCS) of pmCherry-N1 vector.
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
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)DH5alpha
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Growth instructionsXL10-Gold Ultracompetent cells should be used for multiplication of plasmid.
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Copy numberHigh Copy
Gene/Insert 1
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Gene/Insert nameER export signal of Scap
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Alt nameSREBF chaperone (Scap)
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SpeciesCricetulus griseus (Chinese hamster)
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Insert Size (bp)36
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GenBank IDNM_001244036 NP_001230965
- Promoter CMV immediate early promoter
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Tag
/ Fusion Protein
- mCherry (N terminal on insert)
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site BspEI (not destroyed)
- 3′ cloning site BspEI (destroyed during cloning)
- 5′ sequencing primer Forward primer for pEGFPN1 or pmCherryN1
- 3′ sequencing primer Reverse primer for pmCherryN (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameER export signal of Scap
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Alt nameSREBF chaperone (Scap)
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SpeciesCricetulus griseus (Chinese hamster)
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Insert Size (bp)36
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GenBank IDNM_001244036 NP_001230965
- Promoter CMV immediate early promoter
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Tag
/ Fusion Protein
- ER export (N terminal on insert)
Cloning Information for Gene/Insert 2
- Cloning method Restriction Enzyme
- 5′ cloning site BspEI (destroyed during cloning)
- 3′ cloning site BspEI (destroyed during cloning)
- 5′ sequencing primer Forward primer for pEGFPN1 or pmCherryN1
- 3′ sequencing primer Reverse primer for pmCherryN (Common Sequencing Primers)
Gene/Insert 3
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Gene/Insert nameTMD (trans-membrane domain) of Calneuron-2
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Alt namecalcium binding protein 7 (Cabp7)/C-terminal region of Calneuron-2
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SpeciesR. norvegicus (rat)
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Insert Size (bp)87
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GenBank IDNM_001007730 NP_001007731
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Entrez GeneCabp7 (a.k.a. rCaBP7)
- Promoter CMV immediate early promoter
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Tag
/ Fusion Protein
- ER export (N terminal on insert)
Cloning Information for Gene/Insert 3
- Cloning method Restriction Enzyme
- 5′ cloning site BspEI (destroyed during cloning)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer Forward primer for pEGFPN1 or pmCherryN1
- 3′ sequencing primer Reverse primer for pmCherryN (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:
pGolt-mCherry / pGolt3-mCherry was a gift from Michael Kreutz (Addgene plasmid # 73297 ; http://n2t.net/addgene:73297 ; RRID:Addgene_73297) -
For your References section:
A Dendritic Golgi Satellite between ERGIC and Retromer. Mikhaylova M, Bera S, Kobler O, Frischknecht R, Kreutz MR. Cell Rep. 2015 Dec 30. pii: S2211-1247(15)01437-0. doi: 10.1016/j.celrep.2015.12.024. 10.1016/j.celrep.2015.12.024 PubMed 26748700