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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 21359 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCI (modified)
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Backbone manufacturerPromega
- Backbone size w/o insert (bp) 4713
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Vector typeMammalian Expression
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Selectable markersnone
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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Growth instructionsDH5a in dYT at 37oC
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameautosomal dominant polycystic kidney disease type I
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Alt namePKD1 wild-type
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SpeciesH. sapiens (human)
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Insert Size (bp)13117
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Mutationwild-type sequence*
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GenBank IDL33243
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Entrez GenePKD1 (a.k.a. PBP, PC1, Pc-1, TRPP1)
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Tag
/ Fusion Protein
- FLAG (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site SalI (destroyed during cloning)
- 5′ sequencing primer T7 EEV
- 3′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
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Article Citing this Plasmid
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: during Addgene's quality control process, the following mutations were found in PKD1: A691P, M792L, S999P, N1056T, T1724A, M1976V. The depositor has noted that the plasmid appears to be functional using several assays but it is not the standard PKD1 sequence in the database (Genbank ID L33243).
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:
WT (AF20) was a gift from Gregory Germino (Addgene plasmid # 21359 ; http://n2t.net/addgene:21359 ; RRID:Addgene_21359) -
For your References section:
Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations. Qian F, Boletta A, Bhunia AK, Xu H, Liu L, Ahrabi AK, Watnick TJ, Zhou F, Germino GG. Proc Natl Acad Sci U S A. 2002 Dec 24. 99(26):16981-6. 10.1073/pnas.252484899 PubMed 12482949