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Depositing Lab
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Depositing OrganizationInstitut d'Investigacions Biomediques de Barcelona (IIBB-CSIC)
Located in Spain -
Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 45016 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
| DNA | 45016-D50 | 50 μg of DNA in Tris buffer | $495 | ||
| DNA | 45016-D100 | 100 μg of DNA in Tris buffer | $585 | ||
Backbone
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Vector backbonepDEST-R4-R3
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Backbone manufacturerLife Technologies/Invitrogen
- Total vector size (bp) 4511
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Modifications to backboneThe attB1 site resulting from MultiSite Gateway recombination was lost owing to further modification in order to insert the beta-globin intron between the Hspa1b promoter and the mPlum coding sequence.
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Vector typeMammalian Expression
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)Top10
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namemPlum
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SpeciesDiscosoma sp.
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Insert Size (bp)681
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GenBank IDAY786537.1
- Promoter mouse Hspa1b
Cloning Information
- Cloning method Gateway Cloning
- 5′ sequencing primer M13 reverse
- 3′ sequencing primer M13 forward (-20)
- (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byThe original mPlum cDNA for constructing our plasmid was initially provided by Dr Roger Y.Tsien (UCSD), and use was subject to their MTA.
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
Wang L, Jackson WC, Steinbach PA, Tsien RY. Evolution of new nonantibody
proteins via iterative somatic hypermutation. Proc Natl Acad Sci U S A. 2004 Nov
30;101(48):16745-9.
DNA (Catalog # 45016-D50)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 50 μg
- Concentration 1 μg/μL
- Pricing $495 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
DNA (Catalog # 45016-D100)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 100 μg
- Concentration 1 μg/μL
- Pricing $585 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
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:
Hsp70-mplum was a gift from Anna Planas (Addgene plasmid # 45016 ; http://n2t.net/addgene:45016 ; RRID:Addgene_45016) -
For your References section:
In vivo imaging of induction of heat-shock protein-70 gene expression with fluorescence reflectance imaging and intravital confocal microscopy following brain ischaemia in reporter mice. de la Rosa X, Santalucia T, Fortin PY, Purroy J, Calvo M, Salas-Perdomo A, Justicia C, Couillaud F, Planas AM. Eur J Nucl Med Mol Imaging. 2013 Feb;40(3):426-38. doi: 10.1007/s00259-012-2277-7. Epub 2012 Nov 8. 10.1007/s00259-012-2277-7 PubMed 23135322