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Purpose(Empty Backbone) pUC cloning vector
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Depositing Lab
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Publication
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Sequence Information
Ordering
This material is available to academics and nonprofits only.
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 50004 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 | |
Backbone
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Vector backbonepUC6, Addgene plasmid #49793
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Backbone manufacturerMessing Lab
- Backbone size (bp) 2680
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Modifications to backbonepolylinker from M13mp18 (Addgene plasmid #49986) added to polylinker.
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Vector typeBacterial Expression
- Promoter lac
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 numberHigh Copy
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer M13-F20
- 3′ sequencing primer M13R (Common Sequencing Primers)
Resource Information
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Articles 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
Identical to pUC19 (Addgene plasmid #50005) except that the multiple cloning sites (MCS) are arranged in opposite orientation.
How to cite this plasmid
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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:
pUC18 was a gift from Joachim Messing (Addgene plasmid # 50004 ; http://n2t.net/addgene:50004 ; RRID:Addgene_50004) -
For your References section:
Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis. Norrander J, Kempe T, Messing J. Gene. 1983 Dec;26(1):101-6. 10.1016/0378-1119(83)90040-9 PubMed 6323249
Map uploaded by the depositor.
