TIAM1 Blocking Peptide (C-term)
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q13009 |
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Other Accession | Q60610, NP_003244.2 |
Gene ID | 7074 |
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Other Names | T-lymphoma invasion and metastasis-inducing protein 1, TIAM-1, TIAM1 |
Target/Specificity | The synthetic peptide sequence is selected from aa 1493-1506 of HUMAN TIAM1 |
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 | TIAM1 {ECO:0000303|PubMed:7731688, ECO:0000312|HGNC:HGNC:11805} |
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Function | Guanyl-nucleotide exchange factor that activates RHO-like proteins and connects extracellular signals to cytoskeletal activities. Activates RAC1, CDC42, and to a lesser extent RHOA and their downstream signaling to regulate processes like cell adhesion and cell migration. |
Cellular Location | Cell junction. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Note=Detected at the boundary between cells with actin-rich protrusions (By similarity). Presence of KRIT1, CDH5 and RAP1B is required for its localization to the cell junction |
Tissue Location | Found in virtually all analyzed tumor cell lines including B- and T-lymphomas, neuroblastomas, melanomas and carcinomas |
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Provided below are standard protocols that you may find useful for product applications.
Background
Modulates the activity of RHO-like proteins and connects extracellular signals to cytoskeletal activities. Acts as a GDP-dissociation stimulator protein that stimulates the GDP-GTP exchange activity of RHO-like GTPases and activates them. Activates RAC1, CDC42, and to a lesser extent RHOA.
References
Yang, W., et al. Jpn. J. Clin. Oncol. 40(11):1053-1059(2010)
Moriarty, C.H., et al. J. Biol. Chem. 285(27):20541-20546(2010)
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Rajagopal, S., et al. J. Biol. Chem. 285(23):18060-18071(2010)
Shepherd, T.R., et al. J. Mol. Biol. 398(5):730-746(2010)
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