ss-ED-mCherry-GPI
(Plasmid
#163680)
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PurposeExprsses the GPI-anchored luminal domain of ST6GAL1 with a mCherry tag in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 163680 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepmoxGFP-N1
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Backbone manufacturerE. Snapp (Addgene plasmid # 68070)
- Backbone size w/o insert (bp) 3958
- Total vector size (bp) 5965
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Vector typeMammalian 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 nameThe luminal domain of ST6 beta-galactoside alpha-2,6-sialyltransferase 1 with N-terminally tagged signal sequences
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Alt nameST6GAL1
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Alt nameST
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SpeciesH. sapiens (human)
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Insert Size (bp)2007
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MutationThis chimera contains the ecto-domain of ST. Its N-terminus was fused with a signal peptide and C-terminus was tagged with mCherry and GPI anchor.
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GenBank IDBC040009
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Entrez GeneST6GAL1 (a.k.a. CDw75, SIAT1, ST6GalI, ST6N)
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Tags
/ Fusion Proteins
- mCherry (C terminal on insert)
- GPI anchor (C terminal on insert)
- signal sequences (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XhoI (not destroyed)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer CMV-F
- 3′ sequencing primer SV40-PArev (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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:
ss-ED-mCherry-GPI was a gift from Lei Lu (Addgene plasmid # 163680 ; http://n2t.net/addgene:163680 ; RRID:Addgene_163680) -
For your References section:
A quantitative study of the Golgi retention of glycosyltransferases. Sun X, Mahajan D, Chen B, Song Z, Lu L. J Cell Sci. 2021 Oct 15;134(20). pii: 272560. doi: 10.1242/jcs.258564. Epub 2021 Oct 21. 10.1242/jcs.258564 PubMed 34533190