SESTD1 Antibody (N-term) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q86VW0 |
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Clone Names | 91218147 |
Gene ID | 91404 |
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Other Names | SEC14 domain and spectrin repeat-containing protein 1, Huntingtin-interacting protein-like protein, Protein Solo, SESTD1, SOLO |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | SESTD1 |
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Synonyms | SOLO |
Function | May act as the primary docking protein directing membrane turnover and assembly of the transient receptor potential channels TRPC4 and TRPC5. Binds phospholipids such as phosphatidylinositol monophosphates, phosphatidylinositol diphosphates (PIP2s) and phosphatidic acid, but not less polar lipids including phosphatidylcholine, phosphatidylserine, and phosphatidylinositol. The binding to PIP2s is calcium dependent. Might be involved in the plasma membrane localization of CTNNB1. |
Tissue Location | Broad expression. High expression in thalamus and brain. Significantly expressed in vasculature |
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Provided below are standard protocols that you may find useful for product applications.
Background
SESTD1 may act as the primary docking protein directing membrane turnover and assembly of the transient receptor potential channels TRPC4 and TRPC5. Binds phospholipids such as phosphatidylinositol monophosphates, phosphatidylinositol diphosphates (PIP2s) and phosphatidic acid, but not less polar lipids including phosphatidylcholine, phosphatidylserine, and phosphatidylinositol. The binding to PIP2s is calcium dependent. Might be involved in the plasma membrane localization of CTNNB1.
References
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :Miehe, S., et al. J. Biol. Chem. 285(16):12426-12434(2010)Trynka, G., et al. Gut 58(8):1078-1083(2009)Sato, T., et al. Genomics 82(2):218-229(2003)
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