BLA/Xpress
(Plasmid
#1804)
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 1804 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBluescript II KS
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Backbone manufacturerStratagene
- Backbone size w/o insert (bp) 3000
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Vector typeBacterial Expression
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Selectable markersBlasticidin
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
Gene/Insert
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Gene/Insert nameBLA/Xpress
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Insert Size (bp)991
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Tag
/ Fusion Protein
- Xpress (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XbaI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer na (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:
BLA/Xpress was a gift from Christian Tschudi (Addgene plasmid # 1804 ; http://n2t.net/addgene:1804 ; RRID:Addgene_1804) -
For your References section:
In vivo epitope tagging of Trypanosoma brucei genes using a one step PCR-based strategy. Shen S, Arhin GK, Ullu E, Tschudi C. Mol Biochem Parasitol 2001 Mar;113(1):171-3. 10.1016/S0166-6851(00)00383-2 PubMed 11254965