HA-RELT deletion F
(Plasmid
#260224)
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PurposeExpression in mammalian cells
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Depositing Lab
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Depositing OrganizationCalifornia Northstate University
Located in the United States of America -
Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 260224 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
Backbone
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Vector backbonepcDNA3
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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)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameRELT (Receptor Expressed in Lymphoid Tissues)
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SpeciesH. sapiens (human)
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Insert Size (bp)1200
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MutationLacking 30 amino acids from C-terminal end (1-400 of 430)
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Entrez GeneRELT (a.k.a. FLJ14993, TNFRSF19L)
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Tag
/ Fusion Protein
- HA (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Unknown (unknown if destroyed)
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
Please cite: Moua P, Checketts M, Xu LG, Shu HB, Reyland ME, Cusick JK. RELT family members activate p38 and induce apoptosis by a mechanism distinct from TNFR1. Biochem Biophys Res Commun. 2017 Sep 9;491(1):25-32. doi: 10.1016/j.bbrc.2017.07.022. Epub 2017 Jul 5. PMID: 28688764; PMCID: PMC5617334.
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:
HA-RELT deletion F was a gift from John Cusick (Addgene plasmid # 260224 ; http://n2t.net/addgene:260224 ; RRID:Addgene_260224) -
For your References section:
RELT family members activate p38 and induce apoptosis by a mechanism distinct from TNFR1. Moua P, Checketts M, Xu LG, Shu HB, Reyland ME, Cusick JK. Biochem Biophys Res Commun. 2017 Sep 9;491(1):25-32. doi: 10.1016/j.bbrc.2017.07.022. Epub 2017 Jul 5. 10.1016/j.bbrc.2017.07.022 PubMed 28688764