pME GFP-DCX
(Plasmid
#105962)
-
Purposeentry clone for gateway cloning
-
Depositing Lab
-
Publication
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 105962 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonep_DONR221_(P1-P2)
-
Vector typeBacterial Expression
Growth in Bacteria
-
Bacterial Resistance(s)Kanamycin, 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameNP_835365.1
-
SpeciesH. sapiens (human)
-
Entrez GeneDCX (a.k.a. DBCN, DC, LISX, SCLH, XLIS)
-
Tags
/ Fusion Proteins
- 6xHis-thrombin cleavage site (N terminal on insert)
- EGFP (N terminal on insert)
Cloning Information
- Cloning method Gateway Cloning
Terms and Licenses
-
Academic/Nonprofit Terms
-
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.
-
For your Materials & Methods section:
pME GFP-DCX was a gift from Caren Norden (Addgene plasmid # 105962 ; http://n2t.net/addgene:105962 ; RRID:Addgene_105962) -
For your References section:
Independent modes of ganglion cell translocation ensure correct lamination of the zebrafish retina. Icha J, Kunath C, Rocha-Martins M, Norden C. J Cell Biol. 2016 Oct 24;215(2):259-275. 10.1083/jcb.201604095 PubMed 27810916