Recombinant Human CEACAM-3/CD66d Fc Chimera Protein, CF
Recombinant Human CEACAM-3/CD66d Fc Chimera Protein, CF Summary
Product Specifications
Human CEACAM-3 (Lys35-Gly155) Accession # P40198 | IEGRMD | Human IgG1 (Pro100-Lys330) |
N-terminus | C-terminus | |
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
9985-CM
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 500 μg/mL in PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: |
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Scientific Data
When Recombinant Human CEACAM-3/CD66d Fc Chimera (Catalog # 9985-CM) is immobilized at 1 µg/mL, Recombinant Human CEACAM-7 (Catalog # 9010-CM) binds with an ED50 of 0.05-0.4 µg/mL.
2 μg/lane of Recombinant Human CEACAM‑3 was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 48-54 kDa and 96-110 kDa, respectively.
Reconstitution Calculator
Background: CEACAM-3/CD66d
Carcinoembryonic Antigen-related Cell Adhesion Molecule 3 (CEACAM-3), or CD66d, is part of the CEA protein family consisting of CEACAMs and the pregnancy-specific glycoproteins (PSGs). Both CEACAM and PSG molecules have been identified in humans and belong to the much larger glycosylphosphatidylinositol (GPI)-linked immunoglobulin (Ig) superfamily (1, 2). Human CEACAM-3 is ~35 kDa, consisting of an extracellular domain (ECD) containing one IgV-like domain, a single transmembrane domain and a cytoplasmic tail. The cytoplasmic tail of CEACAM-3 contains an immunoreceptor tyrosine-based activation motif (ITAM), which recruits kinases to propagate pro-inflammatory signaling cascades (3). Interestingly, CEACAM-3 appears to be primate specific, with on non-primate orthologs currently identified (4). Originally discovered as a biomarker for colorectal cancer (5), CEACAMs have now been associated with numerous intracellular signaling processes including cell adhesion, cell growth, recognition and differentiation, angiogenesis, and apoptosis (6-8). Unlike other CEA family members, CEACAM-3 has not been shown to form cell–cell adhesion interactions with other CEACAM family members (9). CEACAM-3 has been found to be specifically expressed on human neutrophils and other granulocytes and appears to be a specific adaptation of the innate immune system to cope with a small set of host-specific pathogen (9). CEACAM-3 was identified as critical for opsonin-independent phagocytosis and bacterial clearance (10). CEACAM-3 binds to the colony opacity-associated (Opa) outer membrane proteins of bacteria, such as Neisseria gonorrhoeae, and triggers uptake of the pathogen and subsequent elimination (9, 10).
- Beauchemin, N. et al. (1999) Exp. Cell Res. 252:243.
- Zebhauser R, et al. (2005) Genomics 86:566.
- Schmitter, T. et al. (2004) J. Exp. Med. 199:35.
- Pavlopoulou A. and Scorilas A. (2014) Genome Biol Evol. 6:1314.
- Gold P and Freedman, S.O. (1965) J Exp Med. 122:467.
- Obrink, B. (1997) Curr Opin Cell Biol. 9:616.
- Horst, AK. and Wagener, C. (2004) Handb Exp Pharmacol. 165:283.
- Kuespert K et al. (2006) Curr Opin Cell Biol. 18:565.
- Pils S. et al. (2008) Int J Med Microbiol. 298:553.
- Schmitter, T. et al. (2004) J. Exp. Med. 199:35.
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