aCat DeltaTS (delta570 to 670 aa in aCat TS WT)
(Plasmid
#101300)
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PurposeFRET-based tension sensor (TS) technology to develop a probe for molecular-level tension across alphaE-catenin. See Depositor Comments for plasmid construction.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 101300 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepEGFP-C1
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Vector typeMammalian Expression
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 namealpha-Catenin
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SpeciesM. musculus (mouse)
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MutationContains amino acids 1-509, 670-698, and 699-906 of alpha-Catenin
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer Unknown (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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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.
Depositor Comments
For alpha-CatD-TS, the alpha-Cat-TS was digested with NheI and XmaI to cut out a fragment corresponding to 1-670 aa, and a PCR-amplified fragment corresponding to amino acids 1_509 from mouse aE-catenin was ligated back at the same restriction enzyme sites
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:
aCat DeltaTS (delta570 to 670 aa in aCat TS WT) was a gift from Alpha Yap (Addgene plasmid # 101300 ; http://n2t.net/addgene:101300 ; RRID:Addgene_101300) -
For your References section:
Mammalian Diaphanous 1 Mediates a Pathway for E-cadherin to Stabilize Epithelial Barriers through Junctional Contractility. Acharya BR, Wu SK, Lieu ZZ, Parton RG, Grill SW, Bershadsky AD, Gomez GA, Yap AS. Cell Rep. 2017 Mar 21;18(12):2854-2867. doi: 10.1016/j.celrep.2017.02.078. 10.1016/j.celrep.2017.02.078 PubMed 28329679