Recombinant Human CXADR Fc Chimera Protein, CF Summary
Details of Functionality
Measured by its binding ability in a functional ELISA. Recombinant Human CXADR Fc Chimera (Catalog # 3336-CX) binds Recombinant Human AMICA/JAML Fc Chimera (Catalog #
3449-AM) with an ED50 of 2.50-25.0 ng/mL.
Source
Mouse myeloma cell line, NS0-derived human CXADR protein
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
50.6 kDa (monomer). Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
60-65 kDa, reducing conditions
Publications
Read Publications using 3336-CX in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human CXADR Fc Chimera Protein, CF
CAR10Coxsackievirus B-adenovirus receptor
CAR4/6
coxsackie virus and adenovirus receptor
coxsackie virus B receptor
coxsackievirus and adenovirus receptor
CVB3 binding protein
CVB3 BP
CVB3-binding protein
CXADR
HCAR
HCVADR
Background
CXADR (coxsackie and adenovirus receptor), also known as CAR, is a 46 kDa type I transmembrane glycoprotein that belongs to the CTX family of the Ig superfamily (1 - 3). CXADR has received attention as a receptor that facilitates gene transfer mediated by most adenoviruses (1, 2). It is also an adhesion molecule within junctional complexes, notably between epithelial cells lining body cavities and within myocardial intercalated discs (1, 2, 4). CXADR is essential for normal cardiac development in the mouse (7). It is expressed throughout brain neuroepithelium during development, but mainly in ependymal cells in the adult (4 - 6). The 365 amino acid (aa) human CXADR contains a 19 aa signal sequence, a 218 aa extracellular domain (ECD) with a V-type (D1) and a C2-type (D2) Ig-like domain, a 21 aa transmembrane segment and a 107 aa intracellular domain. D1 is thought to be responsible for homodimer formation in trans within tight junctions (2). The fiber knob of adenoviruses attaches at a similar site, and evidence suggests that disruption of tight junctions facilitates virus binding (1, 2). The C-terminus interacts with several cytoplasmic junctional proteins, microtubules and the actin cytoskeleton (1, 8, 9). CXADR interaction with junctional adhesion molecule-like protein (JAML) has been shown to have important functional roles in immunity, inflammation, and tissue homeostatsis (10).The ECD of human CXADR shares 90% aa sequence identity with mouse, rat, and porcine CXADR, and 92% and 89% aa identity with bovine and canine CXADR, respectively. An alternately spliced isoform (CXADR2) that diverges in the C-terminal 15 aa shows a similar expression pattern (4, 11). Transcription of splice variants that produce soluble forms of CXADR has been detected, and secreted forms in serum and pleural fluid potentially block viral infection (12).
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Philipson, L. and R.F. Pettersson (2004) Curr. Top. Microbiol. Immunol. 273:87.
Tomko, R.P. et al. (1997) Proc. Natl. Acad. Sci. USA 94:3352.
Raschperger, E. et al. (2006) Exp. Cell Res. 312:1566.
Hotta, Y. et al. Dev. Brain Res. 143:1.
Hauwel, M. et al. (2005) Brain Res. Rev. 48:265.
Chen, J. et al. (2006) Circ. Res. 98:923.
Fok, P.T. et al. (2007) J. Biol. Chem. 282:7512.
Huang, K-C. et al. (2007) FEBS Lett. 581:2702.
Verdino, P. et al. Science (2010) Science 329:1210.
Mirza, M. et al. (2006) Exp. Cell Res. 312:817.
Bernal, R.M. et al. (2002) Clin. Cancer Res. 8:1915.
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