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Purposefull length wt mouse Cry1 HA tag in pcDNA3.1
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 110298 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCDNA 3.1 HA tag
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Backbone manufacturergenscript
- Total vector size (bp) 5450
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Vector typeMammalian Expression
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)DH5alpha
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Copy numberLow Copy
Gene/Insert
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Gene/Insert namewt mcry1 HA tag
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Alt namemouse CRY1
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SpeciesM. musculus (mouse)
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Mutationwildtype
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Entrez GeneCry1 (a.k.a. Phll1)
- Promoter CMV
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Tags
/ Fusion Proteins
- HA tag (C terminal on insert)
- HA tag (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site not sure (unknown if destroyed)
- 3′ cloning site not sure (unknown if destroyed)
- 5′ sequencing primer not sure
- 3′ sequencing primer Not sure (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made bynot sure
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.
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:
mCRY1 HA tag was a gift from Joseph Takahashi (Addgene plasmid # 110298 ; http://n2t.net/addgene:110298 ; RRID:Addgene_110298) -
For your References section:
Competing E3 ubiquitin ligases govern circadian periodicity by degradation of CRY in nucleus and cytoplasm. Yoo SH, Mohawk JA, Siepka SM, Shan Y, Huh SK, Hong HK, Kornblum I, Kumar V, Koike N, Xu M, Nussbaum J, Liu X, Chen Z, Chen ZJ, Green CB, Takahashi JS. Cell. 2013 Feb 28;152(5):1091-105. doi: 10.1016/j.cell.2013.01.055. 10.1016/j.cell.2013.01.055 PubMed 23452855