Mouse JAM-A Antibody Summary
Lys27-Ala242
Accession # O88792
Applications
Mouse JAM-A Sandwich Immunoassay
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: JAM-A
The family of junctional adhesion molecules (JAM), comprising at least three members, are type I transmembrane receptors belonging to the immunoglobulin (Ig) superfamily (1, 2). These proteins are localized in the tight junctions between endothelial or epithelial cells. Some family members are also found on blood leukocytes and platelets. Mouse JAM-A is predominantly expressed at intercellular junctions of both epithelial cells and endothelial cells (3). It is also expressed on circulating megakaryocytes. Mouse JAM-A cDNA predicts a 300 amino acid (aa) residue precursor protein with a putative 23 aa signal peptide, a 215 aa extracellular region containing two Ig-like V-subset domains, a 17 aa transmembrane domain and a 45 aa cytoplasmic domain. The human and mouse protein share approximately 67% aa sequence homology. Mouse JAM-A also shares approximately 35% aa sequence homology with mouse JAM-B or JAM-C. JAM-A exhibits homotypic interactions to regulate tight junction assembly and modulate paracellular permeability (1‑3). The human JAM-A homotypic interation also mediates platelet aggregation and adhesion to endothelial cells and may play a role in thrombosis (4). JAM-A is involved in leukocyte adhesion and transmigration through the endothelium (3, 5). JAM-A has also been shown to bind reovirus attachment protein sigma-1 to permit reovirus infection and signal virus-induced apoptosis (6).
- Chavakis, T. et al. (2003) Thromb. Haemost. 89:13.
- Aurand-Lions, M. et al. (2001) Blood 98:3699.
- Martin-Padura, I. et al. (1998) J. Cell Biol. 142:117.
- Babinska, A. et al. (2002) Thromb. Haemost. 88:842.
- Del Maschio, A. et al. (1999) J. Exp. Med. 190:1351.
- Barton, E. S. et al. (2001) Cell 104:441.
Product Datasheets
Citations for Mouse JAM-A Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
9
Citations: Showing 1 - 9
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Dysregulation of intestinal epithelial CFTR-dependent Cl- ion transport and paracellular barrier function drives gastrointestinal symptoms of food-induced anaphylaxis in mice
Authors: A Yamani, D Wu, R Ahrens, L Waggoner, TK Noah, V Garcia-Her, C Ptaschinsk, CA Parkos, NW Lukacs, A Nusrat, SP Hogan
Mucosal Immunol, 2020-06-23;0(0):.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Neutrophil expressed CD47 regulates CD11b/CD18-dependent neutrophil transepithelial migration in the intestine in vivo
Authors: V Azcutia, M Kelm, AC Luissint, K Boerner, S Flemming, M Quiros, G Newton, A Nusrat, FW Luscinskas, CA Parkos
Mucosal Immunol, 2020-06-19;0(0):.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry -
Macrophage-dependent neutrophil recruitment is impaired under conditions of increased intestinal permeability in JAM-A-deficient mice
Authors: AC Luissint, HC Williams, W Kim, S Flemming, V Azcutia, RS Hilgarth, MNO Leary, TL Denning, A Nusrat, CA Parkos
Mucosal Immunol, 2019-02-11;0(0):.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Analysis of leukocyte transepithelial migration using an in vivo murine colonic loop model
Authors: S Flemming, AC Luissint, A Nusrat, CA Parkos
JCI Insight, 2018-10-18;3(20):.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Dysregulation of junctional adhesion molecule-A contributes to ethanol-induced barrier disruption in intestinal epithelial cell monolayers
Authors: DM Chopyk, P Kumar, R Raeman, Y Liu, T Smith, FA Anania
Physiol Rep, 2017-12-01;5(23):.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Murine junctional adhesion molecules JAM-B and JAM-C mediate endothelial and stellate cell interactions during hepatic fibrosis
Authors: E Hintermann, M Bayer, J Ehser, M Aurrand-Li, JM Pfeilschif, BA Imhof, U Christen
Cell Adh Migr, 2016-04-25;10(4):419-33.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr -
Lysosomal protein turnover contributes to the acquisition of TGFbeta-1 induced invasive properties of mammary cancer cells.
Authors: Kern U, Wischnewski V, Biniossek M, Schilling O, Reinheckel T
Mol Cancer, 2015-02-15;14(0):39.
Species: Mouse
Sample Types: Cell Lysates, Whole Cells
Applications: ICC, Western Blot -
Regulated release and functional modulation of junctional adhesion molecule A by disintegrin metalloproteinases.
Authors: Koenen RR, Pruessmeyer J, Soehnlein O, Fraemohs L, Zernecke A, Schwarz N, Reiss K, Sarabi A, Lindbom L, Hackeng TM, Weber C, Ludwig A
Blood, 2009-03-03;113(19):4799-809.
Species: Mouse
Sample Types: Tissue Homogenates
Applications: ELISA Development -
JAM-A is present in mammalian spermatozoa where it is essential for normal motility.
Authors: Shao M, Ghosh A, Cooke VG, Naik UP, Martin-DeLeon PA
Dev. Biol., 2007-10-23;313(1):246-55.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC
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