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Phospho-TJP2(S978) Blocking Peptide

Synthetic peptide

     
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Product Information
Primary Accession Q9UDY2
Other Accession NP_001164101.1
Additional Information
Gene ID 9414
Other Names Tight junction protein ZO-2, Tight junction protein 2, Zona occludens protein 2, Zonula occludens protein 2, TJP2, X104, ZO2
Target/Specificity The synthetic peptide sequence is selected from aa 971-985 of HUMAN TJP2
Format Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name TJP2
Synonyms X104, ZO2
Function Plays a role in tight junctions and adherens junctions (By similarity). Acts as a positive regulator of RANKL-induced osteoclast differentiation, potentially via mediating downstream transcriptional activity (By similarity).
Cellular Location Cell junction, adherens junction. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Cell junction, tight junction {ECO:0000250|UniProtKB:Q9Z0U1}. Nucleus. Note=Also nuclear under environmental stress conditions and in migratory endothelial cells and subconfluent epithelial cell cultures
Tissue Location This protein is found in epithelial cell junctions. Isoform A1 is abundant in the heart and brain. Detected in brain and skeletal muscle. It is present almost exclusively in normal tissues Isoform C1 is expressed at high level in the kidney, pancreas, heart and placenta. Not detected in brain and skeletal muscle. Found in normal as well as in most neoplastic tissues
Research Areas
Citations (0)
citation

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Background

This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutation in this gene have been identified in patients with hypercholanemia. Alternate splicing results in multiple transcript variants.

References

Lechuga, S., et al. Exp. Cell Res. 316(19):3124-3139(2010)
Remue, E., et al. FEBS Lett. 584(19):4175-4180(2010)
Walsh, T., et al. Am. J. Hum. Genet. 87(1):101-109(2010)
Meerschaert, K., et al. Cell. Mol. Life Sci. 66(24):3951-3966(2009)
Fanning, A.S., et al. Ann. N. Y. Acad. Sci. 1165, 113-120 (2009) :

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$ 277.78
Cat# BP3790a
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