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PurposeTol2 transgenesis to express photoactivatable Rac1 under 4xnr UAS promoter
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Depositing Lab
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Depositing OrganizationUniversity of Wisconsin, Madison
Located in United States of America -
Publication
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Citations
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 41878 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
Backbone
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Vector backboneTol2
- Total vector size (bp) 5473
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Vector typeZebrafish 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 numberUnknown
Gene/Insert
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Gene/Insert namephotoactivatable Rac1
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Alt namePA-Rac1
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SpeciesH. sapiens (human)
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MutationRac1 starts at I4 and contains mutations Q61L, E91H and N92H
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Entrez GeneRAC1 (a.k.a. MIG5, MRD48, Rac-1, TC-25, p21-Rac1)
- Promoter 4xnr UAS
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Tags
/ Fusion Proteins
- 6x His (N terminal on insert)
- mCherry (N terminal on insert)
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer n/a
- (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byPA-Rac1 from Klaus Hahn (Addgene Plasmid #22027)
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
Please note that Addgene's sequencing results differ from the full plasmid sequence provided by the depositing laboratory at bp# 895, 920 and 1702. According to the depositing lab, these differences are not a concern for the function of the plasmid.
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:
tol2-4xnr UAS-PA Rac1-mCherry was a gift from Anna Huttenlocher (Addgene plasmid # 41878 ; http://n2t.net/addgene:41878 ; RRID:Addgene_41878)