pMIR-Report-RASA1-3'UTR
(Plasmid
#62575)
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PurposeTranslational Luciferase Reporter containing a 926 bp fragment of the RASA1 3'UTR.
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Depositing Lab
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 62575 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMIR-Report
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Backbone manufacturerAmbion
- Backbone size w/o insert (bp) 6470
- Total vector size (bp) 7396
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Modifications to backboneNone. Cloning Strategy: To construct a WT RASA1 translational reporter, a 926-bp fragment of the RASA1 3′ UTR (from open biosystems, clone ID BC033015) was generated by sequential treatment with BamHI, Klenow fragment, and XbaI. This fragment was inserted into pMIR-REPORT vector that was prepared by sequential treatment with HindIII, Klenow fragment, and SpeI.
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Vector typeLuciferase
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)XL1 Blue
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameRASA1
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Alt nameRAS p21 Activator (GTPase Activating Protein [GAP])
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SpeciesH. sapiens (human)
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Insert Size (bp)926
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Entrez GeneRASA1 (a.k.a. CM-AVM, CMAVM, CMAVM1, GAP, PKWS, RASA, RASGAP, p120, p120GAP, p120RASGAP)
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Tag
/ Fusion Protein
- None
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer M13pUC-Fwd
- 3′ sequencing primer Luc-F (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.
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:
pMIR-Report-RASA1-3'UTR was a gift from Michael Ruppert (Addgene plasmid # 62575 ; http://n2t.net/addgene:62575 ; RRID:Addgene_62575) -
For your References section:
MicroRNAs 206 and 21 cooperate to promote RAS-extracellular signal-regulated kinase signaling by suppressing the translation of RASA1 and SPRED1. Sharma SB, Lin CC, Farrugia MK, McLaughlin SL, Ellis EJ, Brundage KM, Salkeni MA, Ruppert JM. Mol Cell Biol. 2014 Nov 15;34(22):4143-64. doi: 10.1128/MCB.00480-14. Epub 2014 Sep 8. 10.1128/MCB.00480-14 PubMed 25202123