pENTR-D-TOPO-PAmCherry1_160-236-MCS
(Plasmid
#60546)
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PurposeCloning PAmCherry1 C-terminal fragment (RC) for BiFC-PALM
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 60546 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepENTR/D-TOPO
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Backbone manufacturerInvitrogen
- Backbone size w/o insert (bp) 2580
- Total vector size (bp) 2883
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Modifications to backboneAdded flanking MCSs
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Vector typeCloning
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)Top10
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namePAmCherry1 C-terminal fragment
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Alt nameRC160-236
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Insert Size (bp)234
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Mutationamino acids 160-236
Cloning Information
- Cloning method Ligation Independent Cloning
- 5′ sequencing primer M13 forward
- 3′ sequencing primer M13 reverse (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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
Parent plasmid (full-length PAmCherry1 in pENTR) (Addgene plasmid 60608) originally reported in Nan et al., 2013 (PMID:24158481).
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:
pENTR-D-TOPO-PAmCherry1_160-236-MCS was a gift from Xiaolin Nan (Addgene plasmid # 60546 ; http://n2t.net/addgene:60546 ; RRID:Addgene_60546) -
For your References section:
Photoactivated localization microscopy with bimolecular fluorescence complementation (BiFC-PALM) for nanoscale imaging of protein-protein interactions in cells. Nickerson A, Huang T, Lin LJ, Nan X. PLoS One. 2014 Jun 25;9(6):e100589. doi: 10.1371/journal.pone.0100589. eCollection 2014. 10.1371/journal.pone.0100589 PubMed 24963703