pUC18-H1 RNAi
(Plasmid
#87355)
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PurposeRNAi expression vector based on H1 promoter and pUC18 vector backbone
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 87355 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUC18
- Total vector size (bp) 2864
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Modifications to backboneMCS is BglII-XbaI-HinDIII. H1 RNA promoter placed 5' to MCS.
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Vector typeMammalian Expression, RNAi ; shRNA expression vector
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)NEB Stable
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Growth instructionsCan be maintained in E. coli SURE or any other recombination deficient strain
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameH1 RNA Promoter from U87MG glioma cells
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SpeciesH. sapiens (human)
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Insert Size (bp)219
- Promoter H1 RNA
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer M13 reverse sequencing primer
- 3′ sequencing primer M13 forward sequencing primer (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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
H1 RNA promoter cloned from U87MG glioma (brain tumor) cells via RT-PCR. Vector suitable for shRNA studies, particularly for shRNA expression in glioma cells.
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-H1 RNAi was a gift from Saroj Mathupala (Addgene plasmid # 87355 ; http://n2t.net/addgene:87355 ; RRID:Addgene_87355) -
For your References section:
Silencing of monocarboxylate transporters via small interfering ribonucleic acid inhibits glycolysis and induces cell death in malignant glioma: an in vitro study. Mathupala SP, Parajuli P, Sloan AE. Neurosurgery. 2004 Dec;55(6):1410-9; discussion 1419. PubMed 15574223