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PurposeIndicator of caspase-3-like protease activity
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 78907 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCDH
- Backbone size w/o insert (bp) 7378
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Vector typeLentiviral
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Selectable markersPuromycin
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)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameVC3AI
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SpeciesSynthetic
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Insert Size (bp)1213
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MutationS320A, deletion of AA1-200
- Promoter CMV
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Tags
/ Fusion Proteins
- HA (N terminal on insert)
- Myc (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NheI (not destroyed)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer CMV-forward (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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Articles 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
Usage information based on sensor VC3AI: VC3AI has no or little background fluorescence, and its activation depends on the cleavage of sensor sequence of DEVDG. In fact, the sensors containing DXXDG other than DEVDG do not work. However, cells expressing VC3AI may have “background” fluorescence in some conditions, and we can conform the so-called basal fluorescence still results from the cleaved VC3AI, because cells could have a low level of activated caspase3/7 in some conditions depending on cell line and culture condition.
To avoid the possible detectable basal fluorescence, we infect cells with different dilutions of lentivirus and use the stable cell line expressing sensor protein as high as possible but without basal fluorescence for experiments. Notably, the low level of sensor protein expression work poorly. During our investigation, the basal fluorescence often happens on GC3AI, if the sensor protein expression level is high. This is because GC3AI protein is more stable than other sensors.
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:
pCDH-puro-CMV-VC3AI was a gift from Binghui Li (Addgene plasmid # 78907 ; http://n2t.net/addgene:78907 ; RRID:Addgene_78907) -
For your References section:
Visualization of caspase-3-like activity in cells using a genetically encoded fluorescent biosensor activated by protein cleavage. Zhang J, Wang X, Cui W, Wang W, Zhang H, Liu L, Zhang Z, Li Z, Ying G, Zhang N, Li B. Nat Commun. 2013;4:2157. doi: 10.1038/ncomms3157. 10.1038/ncomms3157 PubMed 23857461