pDONR221-kcnj11
(Plasmid
#173139)
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PurposeThis gene was cloned into the gateway middle entry vector. It can be used for generating antisense riboprobe or gene expression using a gateway system.
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 173139 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepDONR221
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Backbone manufacturerInvitrogen
- Backbone size w/o insert (bp) 2550
- Total vector size (bp) 3696
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Vector typePCR cloning vector
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namekcnj11
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Alt nameKir6.2
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SpeciesD. rerio (zebrafish)
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Insert Size (bp)1146
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GenBank IDNM_001039827.1
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Entrez Genekcnj11 (a.k.a. Kir6, kir6.2)
- Promoter No promoter at 5 end; T7 promoter at 3 end.
Cloning Information
- Cloning method Gateway Cloning
- 5′ sequencing primer M13F
- 3′ sequencing primer M13R (Common Sequencing Primers)
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
This gene was cloned from a pool of mixed zebrafish embryos (1-3dpf) using RT-PCR.
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:
pDONR221-kcnj11 was a gift from GuangJun Zhang (Addgene plasmid # 173139 ; http://n2t.net/addgene:173139 ; RRID:Addgene_173139) -
For your References section:
Evolution of inwardly rectifying potassium channels and their gene expression in zebrafish embryos. Silic MR, Murata SH, Park SJ, Zhang G. Dev Dyn. 2021 Sep 23. doi: 10.1002/dvdy.425. 10.1002/dvdy.425 PubMed 34558132