pME-mCherry-24xMBS
(Plasmid
#86242)
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Purpose(Empty Backbone) Middle entry vector for generating MBS tagged RNAs with a fluorescent protein reporter
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 86242 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonePCR8/GW/TOPO (K250020, Invitrogen)
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Backbone manufacturerInvitrogen
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Modifications to backbonepME-mCherry-24xMBS was created by amplifying mCherry with flanking BamHI sites by PCR from p3E-mCherry (Kwan et al., 2007) using p3E-mCherry-BamHI-F+R primers, then ligating into pME-24xMBS
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Vector typeUnspecified
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Tag
/ Fusion Protein
- mCherry-24xMBS (C terminal on insert)
Growth in Bacteria
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Bacterial Resistance(s)Spectinomycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Resource Information
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Addgene Notes
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
Note: due the the repetitive nature of the cassette, Addgene QC did not verify the presence of all 24x MBS; digest results indicate all sites are present based on size.
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:
pME-mCherry-24xMBS was a gift from Florence Marlow (Addgene plasmid # 86242 ; http://n2t.net/addgene:86242 ; RRID:Addgene_86242) -
For your References section:
Dynamic visualization of transcription and RNA subcellular localization in zebrafish. Campbell PD, Chao JA, Singer RH, Marlow FL. Development. 2015 Apr 1;142(7):1368-74. doi: 10.1242/dev.118968. Epub 2015 Mar 10. 10.1242/dev.118968 PubMed 25758462