pET-28a mScarlet
(Plasmid
#178543)
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PurposeThe mScarlet fluorescent protein with an N-terminal 6xHis-tag in pET28a.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 178543 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET28a
- Backbone size w/o insert (bp) 5306
- Total vector size (bp) 6002
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Vector typeBacterial Expression
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 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 namemScarlet
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SpeciesSynthetic; construct
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GenBank IDAPD76535
- Promoter T7
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Tag
/ Fusion Protein
- 6xHis (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NcoI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer taatacgactcactatagg
- 3′ sequencing primer gtggtggtggtggtggtg (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made byAddgene #85066
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
The mScarlet coding sequence was PCR amplified with an N-terminal 6xHis tag from pCytERM_mScarlet_N1 (Addgene #85066) and inserted into the vector fragment of pET28a (Novagen #69864) digested with NcoI and BamHI.
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:
pET-28a mScarlet was a gift from Siegfried Musser (Addgene plasmid # 178543 ; http://n2t.net/addgene:178543 ; RRID:Addgene_178543) -
For your References section:
Oligomerization state of the functional bacterial twin-arginine translocation (Tat) receptor complex. Sharma A, Chowdhury R, Musser SM. Commun Biol. 2022 Sep 19;5(1):988. doi: 10.1038/s42003-022-03952-2. 10.1038/s42003-022-03952-2 PubMed 36123532