ADAM22 Antibody (N-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q9P0K1 |
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Other Accession | NP_068369.1, NP_004185.1, NP_057435.2, NP_068367.1, NP_068368.2 |
Clone Names | 80924040 |
Gene ID | 53616 |
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Other Names | Disintegrin and metalloproteinase domain-containing protein 22, ADAM 22, Metalloproteinase-disintegrin ADAM22-3, Metalloproteinase-like, disintegrin-like, and cysteine-rich protein 2, ADAM22, MDC2 |
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 | ADAM22 |
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Synonyms | MDC2 |
Function | Probable ligand for integrin in the brain. This is a non catalytic metalloprotease-like protein (PubMed:19692335). Involved in regulation of cell adhesion and spreading and in inhibition of cell proliferation. Neuronal receptor for LGI1. |
Cellular Location | Cell membrane; Single-pass type I membrane protein. Cell projection, axon {ECO:0000250|UniProtKB:Q9R1V6} |
Tissue Location | Highly expressed in the brain and in some high- grade but not low-grade gliomas. Detected slightly or not at all in other tissues. |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the ADAM (a disintegrin andmetalloprotease domain) family. Members of this family aremembrane-anchored proteins structurally related to snake venomdisintegrins, and have been implicated in a variety of biologicalprocesses involving cell-cell and cell-matrix interactions,including fertilization, muscle development, and neurogenesis. Thisgene is highly expressed in the brain and may function as anintegrin ligand in the brain. Alternative splicing results inseveral transcript variants.
References
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :Sagane, K., et al. J. Recept. Signal Transduct. Res. 30(2):72-77(2010)Ozkaynak, E., et al. J. Neurosci. 30(10):3857-3864(2010)Gregorio, S.P., et al. Psychiatry Res 165 (1-2), 1-9 (2009) :Sorensen, H.P., et al. Protein Expr. Purif. 61(2):175-183(2008)
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