Human Carcinoembryonic Antigen Related Cell Adhesion Molecule 1 (CEACAM1) CLIA Kit
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Description
Human CEACAM1 Chemiluminescent Immunoassay (CLIA) Kit is a Sandwich Chemiluminescent Immunoassay (CLIA) Kit for use with Serum, plasma and other biological fluids.
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Product specifications
| Category | CLIA Kits |
| Immunogen Target | Carcinoembryonic Antigen Related Cell Adhesion Molecule 1 (CEACAM1) |
| Reactivity | Human |
| Detection Method | Chemiluminescent |
| Assay Data | Quantitative |
| Assay Type | Sandwich |
| Test Range | 1.56 ng/ml - 100 ng/ml |
| Sensitivity | < 0.57 ng/ml |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Size 1 | 96 tests |
| Size 2 | 5 × 96 tests |
| Size 3 | 10 × 96 tests |
| Form | Lyophilized |
| Tested Applications | CLIA |
| Sample Type | Serum, plasma and other biological fluids. |
| Availability | Shipped within 5-20 working days. |
| Storage | Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual. |
| Dry Ice | No |
| Alias | BGP,BGP1,BGPI,BGP-1,CD66a,Carcinoembryonic antigen-related cell adhesion molecule 1 |
| Background | CLIA Kits CEACAM1 |
| Status | RUO |
| Note | The validity for this kit is at least 6 months. Up to 12 months validity can be provided on request. This product is for research use only. The range and sensitivity is subject to change. Please contact us for the latest product information. For accurate results, sample concentrations must be diluted to mid-range of the kit. If you require a specific range, please contact us in advance or write your request in your order comments. Please note that our ELISA and CLIA kits are optimised for detection of native samples, rather than recombinant proteins. We are unable to guarantee detection of recombinant proteins, as they may have different sequences or tertiary structures to the native protein. |
Descripción
CEACAM1 (carcinoembryonic antigen-related cell adhesion molecule 1) is a member of the CEA (carcinoembryonic antigen) family within the immunoglobulin superfamily (IgSF). This molecule plays a central role in intercellular adhesion, immune regulation, and tumor biology. CEACAM1 is highly expressed on various cell types, including epithelial cells, endothelial cells, leukocytes, and certain tumor cells. It is also involved in diverse physiological processes such as cellular differentiation, proliferation, angiogenesis, and immune response modulation. CEACAM1's expression is tightly regulated, often seen in specific tissues such as the liver, kidneys, and lungs, and it is known to be upregulated during certain immune responses and pathological conditions like inflammation and cancer. This protein has become a subject of interest due to its diverse biological functions, particularly in immune regulation and its role in tumor suppression or tumor progression, depending on the cellular context.
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CEACAM1 Antibody is a Rabbit Polyclonal antibody against CEACAM1. This gene encodes a member of the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily. Two subgroups of the CEA family, the CEA cell adhesion molecules and the pregnancy-specific glycoproteins, are located within a 1.2 Mb cluster on the long arm of chromosome 19. Eleven pseudogenes of the CEA cell adhesion molecule subgroup are also found in the cluster. The encoded protein was originally described in bile ducts of liver as biliary glycoprotein. Subsequently, it was found to be a cell-cell adhesion molecule detected on leukocytes, epithelia, and endothelia. The encoded protein mediates cell adhesion via homophilic as well as heterophilic binding to other proteins of the subgroup. Multiple cellular activities have been attributed to the encoded protein, including roles in the differentiation and arrangement of tissue three-dimensional structure, angiogenesis, apoptosis, tumor suppression, metastasis, and the modulation of innate and adaptive immune responses. Multiple transcript variants encoding different isoforms have been reported, but the full-length nature of all variants has not been defined.
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