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Recombinant Human CXADR Fc Chimera Protein, CF

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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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
Human CXADR
(Leu20 - Gly237)
Accession # P78310
IEGRMD Human IgG1
(Pro100 - Lys330)
N-terminus C-terminus
Accession #
N-terminal Sequence
Leu20
Structure / Form
Disulfide-linked homodimer
Protein/Peptide Type
Recombinant Proteins
Gene
CXADR
Purity
>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:

Packaging, Storage & Formulations

Storage
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).

  1. Coyne, C.B. and J.M. Bergelson (2005) Adv. Drug Deliv. Rev. 57:869.
  2. Philipson, L. and R.F. Pettersson (2004) Curr. Top. Microbiol. Immunol. 273:87.
  3. Tomko, R.P. et al. (1997) Proc. Natl. Acad. Sci. USA 94:3352.
  4. Raschperger, E. et al. (2006) Exp. Cell Res. 312:1566.
  5. Hotta, Y. et al. Dev. Brain Res. 143:1.
  6. Hauwel, M. et al. (2005) Brain Res. Rev. 48:265.
  7. Chen, J. et al. (2006) Circ. Res. 98:923.
  8. Fok, P.T. et al. (2007) J. Biol. Chem. 282:7512.
  9. Huang, K-C. et al. (2007) FEBS Lett. 581:2702.
  10. Verdino, P. et al. Science (2010) Science 329:1210.
  11. Mirza, M. et al. (2006) Exp. Cell Res. 312:817.
  12. Bernal, R.M. et al. (2002) Clin. Cancer Res. 8:1915.

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Publications for CXADR (3336-CX)(6)

We have publications tested in 2 confirmed species: Human, N/A.

We have publications tested in 2 applications: Bioassay, Surface Plasmon Resonance.


Filter By Application
Bioassay
(4)
Surface Plasmon Resonance
(2)
All Applications
Filter By Species
Human
(3)
N/A
(1)
All Species
Showing Publications 1 - 6 of 6.
Publications using 3336-CX Applications Species
P Jayabal, F Zhou, X Ma, KM Bondra, B Blackman, ST Weintraub, Y Chen, P Chévez-Bar, PJ Houghton, B Gallie, Y Shiio Nitric oxide suppression by secreted frizzled-related protein 2 drives retinoblastoma Cell Reports, 2023-02-10;42(2):112103. 2023-02-10 [PMID: 36773293] (Bioassay, N/A) Bioassay N/A
S Eschweiler, A Wang, C Ramírez-Su, A von Witzle, Y Li, SJ Chee, H Simon, M Mondal, M Ellis, GJ Thomas, V Chandra, CH Ottensmeie, P Vijayanand JAML immunotherapy targets recently activated tumor-infiltrating CD8+ T�cells Cell Reports, 2023-01-25;42(2):112040. 2023-01-25 [PMID: 36701231] (Bioassay, Human) Bioassay Human
A Rajan, E Palm, F Trulsson, S Mundigl, M Becker, BD Persson, L Frängsmyr, A Lenman Heparan Sulfate Is a Cellular Receptor for Enteric Human Adenoviruses Viruses, 2021-02-14;13(2):. 2021-02-14 [PMID: 33672966] (Surface Plasmon Resonance, Human) Surface Plasmon Resonance Human
AT Baker, A Greenshiel, L Coughlan, JA Davies, H Uusi-Kertt, DK Cole, PJ Rizkallah, AL Parker Diversity within the adenovirus fiber knob hypervariable loops influences primary receptor interactions Nat Commun, 2019-02-14;10(1):741. 2019-02-14 [PMID: 30765704] (Surface Plasmon Resonance, Human) Surface Plasmon Resonance Human
Lenman A, Liaci A, Liu Y, Ardahl C, Rajan A, Nilsson E, Bradford W, Kaeshammer L, Jones M, Frangsmyr L, Feizi T, Stehle T, Arnberg N Human adenovirus 52 uses sialic acid-containing glycoproteins and the coxsackie and adenovirus receptor for binding to target cells. PLoS Pathog, 2015-02-12;11(2):e1004657. 2015-02-12 [PMID: 25674795] (Bioassay) Bioassay
Ivie SE, Fennessey CM, Sheng J, Rubin DH, McClain MS Gene-trap mutagenesis identifies mammalian genes contributing to intoxication by Clostridium perfringens epsilon-toxin. PLoS ONE, 2011-03-11;6(3):e17787. 2011-03-11 [PMID: 21412435] (Bioassay) Bioassay

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Bioinformatics

Gene Symbol CXADR
Uniprot