pmTagBFP2-C1
(Plasmid
#34634)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 34634 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepC1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4014
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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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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namemTagBFP2
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Insert Size (bp)711
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MutationI174A compared to mTagBFP
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NheI (not destroyed)
- 3′ cloning site BglII (not destroyed)
- 5′ sequencing primer 5'-cggtaggcgtgtacggtgggag-3'
- 3′ sequencing primer 5'-gttcagggggaggtgtgggagg-3' (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.
Depositor Comments
There is an 11bp deletion in Addgene's sequencing results relative to the full plasmid sequence. This gap in alignment between nucleotides 595 and 606 results in a loss of AfeI and AgeI sites but does not influence expression of mTagBFP2 in mammalian cells.
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:
pmTagBFP2-C1 was a gift from Vladislav Verkhusha (Addgene plasmid # 34634) -
For your References section:
An enhanced monomeric blue fluorescent protein with the high chemical stability of the chromophore. Subach OM, Cranfill PJ, Davidson MW, Verkhusha VV. PLoS One. 2011;6(12):e28674. Epub 2011 Dec 8. 10.1371/journal.pone.0028674 PubMed 22174863