|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||37677||Plasmid sent as bacteria in agar stab||1||$65|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 5446
Vector typeMammalian Expression
Selectable markersNeomycin (select with G418)
Growth in Bacteria
SpeciesM. musculus (mouse)
Mutationsoluble form (see comments)
Entrez GeneShh (a.k.a. 9530036O11Rik, Dsh, Hhg1, Hx, Hxl3, M100081, ShhNC)
- Promoter CMV
/ Fusion Protein
- renilla luciferase (C terminal on insert)
- Cloning method Restriction Enzyme
- 5′ cloning site unknown (unknown if destroyed)
- 3′ cloning site unknown (unknown if destroyed)
- 5′ sequencing primer CMV-Fwd
- 3′ sequencing primer BGH-Rev (Common Sequencing Primers)
The ShhN construct contains a stop codon following the site of internal cleavage and therefore produces a protein (ShhN) containing the same amino acid residues as the processed protein but lacking cholesterol modification.
Renilla luciferase was inserted in-frame into the amino-terminal signaling domain located in a peripheral loop within the structure of ShhN.
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.
For your Materials & Methods section:pcDNA3-ShhN-Ren was a gift from Philip Beachy (Addgene plasmid # 37677)
For your References section:Hedgehog-mediated patterning of the mammalian embryo requires transporter-like function of dispatched. Ma Y, Erkner A, Gong R, Yao S, Taipale J, Basler K, Beachy PA. Cell. 2002 Oct 4;111(1):63-75. 10.1016/S0092-8674(02)00977-7 PubMed 12372301