2Bc-T MBP_BoMoC(ed)_W403A_6xH
(Plasmid
#185712)
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PurposeRecombinant B. mori truncated R2 RT expression
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 185712 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET His6 LIC cloning vector (2Bc-T)
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Backbone manufacturerScott Gradia
- Backbone size w/o insert (bp) 5899
- Total vector size (bp) 8419
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Modifications to backboneModified to include an N-terminal MBP tag
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Vector typeBacterial 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)DH5alpha
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameB. mori truncated R2 RT
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Alt nameBoMoC
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SpeciesBombyx mori
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Insert Size (bp)2520
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MutationChanged W403 to A
- Promoter T7
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Tags
/ Fusion Proteins
- MBP (N terminal on insert)
- 6xHis (C terminal on insert)
Cloning Information
- Cloning method Ligation Independent Cloning
- 5′ sequencing primer T7 promoter
- 3′ sequencing primer T7 terminator (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:
2Bc-T MBP_BoMoC(ed)_W403A_6xH was a gift from Kathleen Collins (Addgene plasmid # 185712 ; http://n2t.net/addgene:185712 ; RRID:Addgene_185712) -
For your References section:
Separable structural requirements for cDNA synthesis, nontemplated extension, and template jumping by a non-LTR retroelement reverse transcriptase. Pimentel SC, Upton HE, Collins K. J Biol Chem. 2022 Mar;298(3):101624. doi: 10.1016/j.jbc.2022.101624. Epub 2022 Jan 21. 10.1016/j.jbc.2022.101624 PubMed 35065960