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FCAR / CD89 Protein (His Tag)
| Catalog | Size (Price) | Quantity | In Stock | Operation | Other Information |
| 10414-H08H |
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YES |
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Fc Fragment of IgA Protein Datasheet
CD89 / FCAR Protein Price Information
- 500ug: Inquiring Price;
- ≥1mg Bulk: Inquiring Price
CD89 / FCAR Protein Product Information
| CD89 Synonym: | FCAR,XXbac-BPG230H20.5, CD89 |
| Protein Construction: | A DNA sequence encoding the pro form of human FCAR extracellular domain (NP_001991.1) (Met 1- Asn 227 ) was expressed with a C-terminal polyhistidine tag. |
| Source: | Human |
| Expression Host: | Human Cells |
CD89 / FCAR Protein QC Testing
| Purity: | > 97%, as determined by SDS-PAGE | SDS-PAGE:![]() |
| Endotoxin: | < 1.0 EU per 1μg of the protein as determined by the LAL method. | |
| Stability: | Samples are stable for up to twelve months from date of receipt at -70℃ | |
| Predicted N terminal: | Gln 22 | |
| Molecular Mass: | The secreted recombinant human CD89 is a monomeric protein consisting of 217 amino acids and predicts a molecular mass of 25 kDa. The apparent molecular mass of rhCD89 is approximately 45-50 kDa in SDS-PAGE under reducing conditions. | |
| Formulation: | Lyophilized from sterile PBS , pH 7.4
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CD89 / FCAR Protein Usage Guide
| Storage: | Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage and usage. Avoid repeated freeze-thaw cycles. |
| Reconstitution: | A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information. |
CD89 / FCAR Protein Related Products & Topics
Related Areas:
Immunology>>Cluster of Differentiation>>Granulocyte CD Antigen>>Eosinophils / Neutrophils>>CD89/ FCAR
Immunology>>Cluster of Differentiation>>Monocyte/Macrophage CD Antigen>>Other>>CD89/ FCAR
Immunology>>Fc Receptor>>CD89/ FCAR
Proteins:
| Molecule | Species | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| CD89/FCAR | Human | CD89/FCAR Protein, Recombinant | 10414-H08H |
| CD89/FCAR | Rat | CD89/FCAR Protein, Recombinant | 80014-R08H |
Antibodies:
| Molecule | Application | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| Human CD89/FCAR |
ELISA | Mouse Monoclonal Antibody | 10414-MM02 |
| Human CD89/FCAR |
WB, ELISA | CD89/FCAR Antibody, Rabbit MAb | 10414-R006 |
| Human CD89/FCAR |
WB, ELISA | Rabbit Polyclonal Antibody | 10414-RP01 |
| Human CD89/FCAR |
WB, ELISA | Rabbit Polyclonal Antibody (Antigen Affinity Purified) | 10414-RP02 |
CD89 / FCAR Protein Description
FCAR, also called FcαRI or CD89, is a type I transmembrane receptor for Fc region of IgA which is the most abundant immunoglobulin in mucosal areas but is only the second most common antibody isotype in serum. This receptor is present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, especially phagocytes located in mucosal areas. Upon ligand IgA binding, FcαRI associates with the FcR γ signaling molecule bearing the immunoreceptor tyrosine-based activation motif (ITAM) through a unique charge-based mechanism and triggers multiple cell-mediated immune responses. It has been reported that Fc RI is a dual-function receptor that can mediate both inflammatory and anti-inflammatory responses depending on the type of interaction with its ligand. Sustained aggregation of FCAR results in activation of target-cell functions such as antigen presentation and cytokine release. In contrast, Monomeric targeting with serum IgA or with a variety of anti-FcαRI Fab fragments triggers an inhibitory response and additionally induces apoptosis. FcαRI thus play an fundamental role in preventing tumor development and growth, as well as in controlling inflammation.
References
- Maliszewski, C.R. et al., 1990, J. Exp. Med. 172: 1665-1672.
- Launay, P. et al., 1999, J. Biol. Chem. 274: 7216-7225.
- Monteiro, R.C. et al., 2003, Annu. Rev. Immunol. 21: 177-204.
- Otten, M.A. et al., 2005, J. Immunol. 174: 5472-5480.
- Pasquier, B. et al., 2005, Immunity. 22:31-42.
- Kanamaru, Y. et al., 2007, Blood. 109: 203-211.
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