Recombinant Human CEACAM-7 Protein, CF Summary
| Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Human CEACAM-7 is
immobilized at 0.1 µg/mL
(100 µL/well), the concentration of
Recombinant Human CEACAM-1/CD66a (Catalog # 2244-CM)
that
produces 50% of the optimal binding response is approximately 1.6-8 ng/mL. |
| Source |
Chinese Hamster Ovary cell line, CHO-derived human CEACAM-7 protein Thr36-Asn233, with a C-terminal 6-His tag |
| Accession # |
|
| N-terminal Sequence |
Thr36 |
| Protein/Peptide Type |
Recombinant Proteins |
| Gene |
CEACAM7 |
| Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining |
| Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
| Dilutions |
|
| Theoretical MW |
23 kDa. 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 |
42-52 kDa, reducing conditions
|
Packaging, Storage & Formulations
| Storage |
|
| Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS |
| Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining |
| Reconstitution Instructions |
Reconstitute at 500 μg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human CEACAM-7 Protein, CF
Background
Carcinoembryonic antigen-related cell adhesion molecule 7 (CEACAM-7), also known as CGM2, is an approximately 40 kDa GPI-anchored glycoprotein in the CEACAM family of adhesion molecules (1). Mature human CEACAM-7 consists of two Ig-like domains followed by the GPI anchor (2). Alternative splicing generates a short isoform that lacks the second Ig-like domain. CEACAM-7 is preferentially expressed on the luminal surface of epithelial cells near the mouth of colonic crypts and on pancreatic ductal epithelial cells (3, 4). It is down-regulated during colorectal adenoma progression (2-6) but can be up-regulated during the development of gastric carcinoma (7). R&D Systems in-house testing indicates that CEACAM-7 binds to CEACAM-1, consistent with the heterophilic interaction of CEACAM-1 with other CEACAM family members (1, 8, 9).
- Tchoupa, A.K. et al. (2014) Cell Commun. Signal. 12:27.
- Thompson, J. et al. (1994) J. Biol. Chem. 269:32924.
- Thompson, J. et al. (1997) Cancer Res. 57:1776.
- Scholzel, S. et al. (2000) Am. J. Pathol. 156:595.
- Nollau, P. et al. (1997) Cancer Res. 57:2354.
- Nollau, P. et al. (1997) Am. J. Pathol. 151:521.
- Zhou, J. et al. (2011) World J. Surgical Oncol. 9:172.
- Markel, G. et al. (2004) J. Immunol. 173:3732.
- Oikawa, S. et al. (1992) Biochem. Biophys. Res. Commun. 186:881.
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