PPIL5 Antibody (Center) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q96L50 |
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Clone Names | 110811174 |
Gene ID | 122769 |
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Other Names | Leucine-rich repeat protein 1, 4-1BB-mediated-signaling molecule, 4-1BBlrr, LRR-repeat protein 1, LRR-1, Peptidylprolyl isomerase-like 5, LRR1, PPIL5 |
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 | LRR1 (HGNC:19742) |
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Synonyms | PPIL5 |
Function | Substrate recognition subunit of an ECS (Elongin BC-CUL2/5- SOCS-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins (PubMed:15601820). ECS(LRR1) ubiquitinates MCM7 and promotes CMG replisome disassembly by VCP and chromatin extraction during S- phase (By similarity). May negatively regulate the 4-1BB-mediated signaling cascades which result in the activation of NK-kappaB and JNK1 (PubMed:11804328). |
Cellular Location | Nucleus. |
Tissue Location | Ubiquitous. Maximal expression was seen in the heart and skeletal muscle and minimal expression seen in the kidney |
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Provided below are standard protocols that you may find useful for product applications.
Background
The protein encoded by this gene contains a leucine-richrepeat (LRR). It specifically interacts with TNFRSF9/4-1BB, amember of the tumor necrosis factor receptor (TNFR) superfamily.Overexpression of this gene suppresses the activation of NF-kappa Binduced by TNFRSF9 or TNF receptor-associated factor 2 (TRAF2),which suggests that this protein is a negative regulator ofTNFRSF9-mediated signaling cascades. At least three alternativelyspliced transcript variants encoding distinct isoforms have beenobserved.
References
Jang, L.K., et al. Mol. Cells 12(3):304-312(2001)
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