详细说明
Purity
>95%, by SDS-PAGE with silver staining
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
Activity
Measured by its binding ability in a functional ELISA. When Recombinant Mouse E-Cadherin Fc Chimera (Catalog # ) is coated at 2 μg/mL, Recombinant Mouse Integrin alpha E beta 7 binds with an apparent K d <2.5 nM.
Source
Chinese Hamster Ovary cell line, CHO-derived
Mouse Integrin alpha E
(Phe20-Arg1113, Ser453Gly)
Accession # ABD49099His-Pro GGGSGGGS Acidic Tail 6-His tag Mouse Integrin beta 7
(Glu20-Arg724)
Accession # P26011GGGSGGGS Basic Tail N-terminus C-terminus Accession #
N-terminal Sequence
AnalysisPhe20 & Thr183 ( alpha E), Glu20 ( beta 7)
Structure / Form
Non-covalent heterodimer
Predicted Molecular Mass
130 kDa ( alpha E), 84 kDa ( beta 7)
SDS-PAGE
112-128 kDa and 142-176 kDa, reducing conditions
8356-A3 |
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Formulation Lyophilized from a 0.2 μm filtered solution in PBS. | ||
Reconstitution Reconstitute at 500 μg/mL in sterile PBS. | ||
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. | ||
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Background: Integrin alpha E beta 7
Integrin alpha E beta 7 (also called M290 in mouse and HML-1 in human) is a type I transmembrane adhesion protein. It is composed of an alpha E subunit (epithelial-associated; also designated as CD103) which is expressed as disulfide-linked 150 kDa and 25 kDa heavy and light chains, and a non-covalently associated 130 kDa beta 7 glycoprotein subunit (1, 2). Each subunit has a transmembrane sequence and a short cytoplasmic tail. Integrin alpha E beta 7 is the only known integrin family receptor containing the alpha E subunit, while the beta 7 subunit is also a component of Integrin alpha 4 beta 7 (1-3). The alpha E extracellular domain (ECD) contains 7 beta -propeller domains surrounding an I domain followed by domains called tight, calf-1 and calf-2. An extra X domain, not found in any other alpha integrin, is also present and contains a proteolytic cleavage site (1, 2). The beta 7 ECD contains a vWFA domain, which interacts with the alpha E beta -propeller to form a binding domain. The MIDAS motif (metal ion dependent adhesion site) is critical for binding of alpha E beta 7 to its ligand, E-Cadherin (4). The 1093 amino acid (aa) mouse alpha E extracellular domain shares 79% and 99% aa sequence identity with human and rat alpha E respectively, while the 704 aa mouse beta 7 ECD shares 87% and 94% aa identity with human and rat beta 7, respectively. Integrin alpha E beta 7 is mainly restricted to mucosal tissues, where it engages E-Cadherin (4-6). It was first identified as a marker of intestinal intra-epithelial lymphocytes (1, 5, 6). It has since been recognized that a variety of leukocytes, such as cytotoxic CD8+ T cells, some dendritic cells, and effector/memory-like regulatory T cells, acquire Integrin alpha E beta 7 in the days following their migration to epithelium in the intestines, lungs, and tonsils (6-13). In these tissues Integrin alpha E beta 7 facilitates immune surveillance, including the destruction of infected or transformed epithelial cells and the induction of T cell adaptive responses (7-13). Pathologically, Integrin alpha E beta 7 may be involved in allograft rejection of transplanted pancreatic islets and other tissues (14).
References:
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Smyth, L.J.C. et al. (2007) Clin. Exp. Immunol. 149:162.
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del Rio, M.-L. et al. (2008) J. Immunol. 181:6178.
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Siewert, C. et al. (2008) J. Immunol. 180:146.
Feng, Y. et al. (2002) J. Exp. Med. 196:877.
Alternate Names:
Integrin alpha E beta 7