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Purposemammalian expression vector for MARK2 with a C-terminal eGFP
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Depositing Labs
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Depositing OrganizationOregon Health & Science University
Located in United States of America -
Publication
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Citations
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 66706 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
| DNA | 66706-D50 | 50 μg of DNA in Tris buffer | $495 | ||
| DNA | 66706-D100 | 100 μg of DNA in Tris buffer | $585 | ||
Backbone
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Vector backbonepBa-eGFP
- Backbone size w/o insert (bp) 6732
- Total vector size (bp) 8967
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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)Stbl3
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameMARK2
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Alt namemicrotubule affinity-regulating kinase 2
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Alt nameMAP/microtubule affinity-regulating kinase 2
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Alt nameSerine/threonine-protein kinase MARK2
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SpeciesH. sapiens (human)
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Insert Size (bp)2235
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GenBank IDNM_004954 NP_004945.4
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Entrez GeneMARK2 (a.k.a. EMK-1, EMK1, PAR-1, Par-1b, Par1b)
- Promoter chicken beta actin
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Tag
/ Fusion Protein
- eGFP (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BlnI-blunted on vector, PsiI on insert (destroyed during cloning)
- 3′ cloning site BlnI-blunted on vector, PsiI on insert (destroyed during cloning)
- 5′ sequencing primer TTCGGCTTCTGGCGTGTGAC
- 3′ sequencing primer AGCTTGCCGGTGGTGCAGAT
- (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byFrom Addgene (Plasmid #23404 from William Hahn) which contained 2bp deletion causing a frame shift. This was repaired by PCR and Restriction sites: 5' ClaI and 3' Bsu36I. Both sites remain. Sequence of primer to verify repair 5'-AACCTCAAGGAGCTGCGGGAAC-3'
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
pBa vector is susceptable to recombination and should not be grown in fast growing bacteria or cloned using recombination.
XL 10-Gold, Stbl3, OmniMax2, DH5alpha, and XL 1-Blue are suitable growth strains.
DNA (Catalog # 66706-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 # 66706-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:
pBa-MARK2-eGFP was a gift from Gary Banker & Marvin Bentley (Addgene plasmid # 66706 ; http://n2t.net/addgene:66706 ; RRID:Addgene_66706)