pcDNA3-mRuby2-MACROD1_d77
(Plasmid
#172588)
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PurposeFor transient expression of C-terminal mRuby2-tagged MACROD1del1-77
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 172588 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3-mRuby2
- Backbone size w/o insert (bp) 6140
- Total vector size (bp) 6888
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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)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
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Gene/Insert nameMACROD1
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Alt nameLRP16
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SpeciesH. sapiens (human)
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Insert Size (bp)750
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Mutationdeleted amino acids 1-76
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Entrez GeneMACROD1 (a.k.a. LRP16)
- Promoter CMV
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Tag
/ Fusion Protein
- mRuby2 (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site NheI (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer BGHrev (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:
pcDNA3-mRuby2-MACROD1_d77 was a gift from Karla Feijs (Addgene plasmid # 172588 ; http://n2t.net/addgene:172588 ; RRID:Addgene_172588) -
For your References section:
Comparative analysis of MACROD1, MACROD2 and TARG1 expression, localisation and interactome. Zaja R, Aydin G, Lippok BE, Feederle R, Luscher B, Feijs KLH. Sci Rep. 2020 May 19;10(1):8286. doi: 10.1038/s41598-020-64623-y. 10.1038/s41598-020-64623-y PubMed 32427867