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CEACAM1 encodes a member of the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily. Additionally we are shipping Carcinoembryonic Antigen-Related Cell Adhesion Molecule 1 (Biliary Glycoprotein) Proteins (31) and Carcinoembryonic Antigen-Related Cell Adhesion Molecule 1 (Biliary Glycoprotein) Kits (20) and many more products for this protein.
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Human Monoclonal CEACAM1 Primary Antibody for cELISA, FACS - ABIN108725
Sémiramoth, Gleizes, Turbica, Sandré, Gorges, Kansau, Servin, Chollet-Martin: Escherichia coli type 1 pili trigger late IL-8 production by neutrophil-like differentiated PLB-985 cells through a Src family kinase- and MAPK-dependent mechanism. in Journal of leukocyte biology 2009
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Human Monoclonal CEACAM1 Primary Antibody for EIA, FACS - ABIN114594
Hammarström: The carcinoembryonic antigen (CEA) family: structures, suggested functions and expression in normal and malignant tissues. in Seminars in cancer biology 1999
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Mouse (Murine) Monoclonal CEACAM1 Primary Antibody for FACS - ABIN2663557
Hemmila, Turbide, Olson, Jothy, Holmes, Beauchemin: Ceacam1a-/- mice are completely resistant to infection by murine coronavirus mouse hepatitis virus A59. in Journal of virology 2004
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Human Polyclonal CEACAM1 Primary Antibody for EIA, FACS - ABIN616010
Kilic, Oliveira-Ferrer, Neshat-Vahid, Irmak, Obst-Pernberg, Wurmbach, Loges, Kilic, Weil, Lauke, Tilki, Singer, Ergün: Lymphatic reprogramming of microvascular endothelial cells by CEA-related cell adhesion molecule-1 via interaction with VEGFR-3 and Prox1. in Blood 2007
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Human Polyclonal CEACAM1 Primary Antibody for EIA, FACS - ABIN616012
Oliveira-Ferrer, Tilki, Ziegeler, Hauschild, Loges, Irmak, Kilic, Huland, Friedrich, Ergün: Dual role of carcinoembryonic antigen-related cell adhesion molecule 1 in angiogenesis and invasion of human urinary bladder cancer. in Cancer research 2004
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our data show that human and bovine CEACAM1 can both inhibit NK-cell cytotoxicity although they differ in their intracellular signaling motifs
Data from cultured aortic endothelial cells suggest that CEACAM1 is involved in regulation of vascular endothelial cell reactions to oxidative stress/lipid peroxidation and in regulation of nitric oxide production in large vessels such as aorta.
This data represents the first report of a functional link between CEACAM1 and the VEGFR2 (show KDR Antibodies)/Akt (show AKT1 Antibodies)/eNOS (show NOS3 Antibodies)-mediated vascular permeability pathway.
CEACAM1 has two alleles and serves as a pathogen receptor in cattle.
hepatic CEACAM1 expression at fasting is mediated by Pparalpha (show PPARA Antibodies)-dependent mechanisms.
Gram-positive bacteria promote the mRNA expression of CEACAM1 or CEACAM20 in the small intestine. Inflammatory cytokines or butyrate likely participates in such effects of commensal bacteria.
CEACAM1 is a crucial regulator of B-cell survival, influencing B-cell numbers and protective antiviral antibody responses
High-fat diet amplifies the permissive effect of Ceacam1 deletion on renal expression of all renin (show REN Antibodies)-angiotensin system components, PI3K phosphorylation, inflammation, and fibrosis.
Ceacam1L acts as a crucial factor in glioblastoma-initiating cell maintenance and tumorigenesis by activating c-Src (show SRC Antibodies)/STAT3 (show STAT3 Antibodies) signaling. Monomers of the cytoplasmic domain of Ceacam1L bound to c-Src (show SRC Antibodies) and STAT3 (show STAT3 Antibodies) and induced their phosphorylation.
CEACAM1 levels in the liver were reduced in prenatally stressed diet-induced obesity offspring after the high fat diet challenge, suggesting that preexisting genetic predisposition combined with prenatal stress increases the risk for obesity in adulthood.
high-fat diet reduced hepatic CEACAM1 expression and that overexpressing CEACAM1 in liver curtailed diet-induced metabolic abnormalities by protecting hepatic insulin (show INS Antibodies) clearance.
a physiologic role of CEACAM1 in the regulation of osteoclastogenesis
CD66a and CD117 may be useful markers to isolate several cell types consisting of SMG (show SNRPG Antibodies) epithelium and to analyze their molecular and cellular nature.
This is the first study demonstrating that CEACAM1 enhances vascular remodeling and tuft regression by increasing endothelial resistance to alterations in oxygen tension, thus accelerating vascular recovery after systemic hypoxia.
CEACAM1 might play an important role in ovarian tumor progression, especially in tumor metastasis
Osteosarcoma patients with higher CEACAM1 had relatively lower survival compared to those with low CEACAM1 and high serum CEACAM1 level was an independent prognostic factor for osteosarcoma
serum CEACAM1 is elevated over time in progressive melanoma patients who fail to respond to immunotherapy as opposed to responders and stable disease patients.
an MITF (show MITF Antibodies)-CEACAM1 axis is suggested as a potential determinant of melanoma progression.
Collectively, these data suggest that vIL (show VIL1 Antibodies)-6 modulates endothelial cell migration by upregulating the expression of cellular factors, including CEACAM1.
Taken together, our results demonstrate a systematic down-regulation of CEACAM1 in breast cancer and suggest that a strategy to restore CEACAM1 expression may be helpful for the treatment of breast cancer.
Elevated carcinoembryonic antigen (show CEACAM5 Antibodies) expression is associated with recurrence for patients after resection for colorectal liver metastases.
Serum concentrations of CEACAM1 may serve as a useful indicator for the presence of breast cancer
High Carcinoembryonic Antigen (show CEACAM5 Antibodies) expression is associated with colon and stomach cancer.
High carcinoembryonic antigen (show CEACAM5 Antibodies) serum levels are associated with Lung Adenocarcinoma.
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.
carcinoembryonic antigen-related cell adhesion molecule 1
, carcinoembryonic antigen-related cell adhesion molecule 8
, CEA-related cell adhesion molecule 1
, biliary glycoprotein 1
, biliary glycoprotein D
, carcinoembryonic antigen 1
, carcinoembryonic antigen 7
, hepatitis virus (MHV-4) susceptibility
, hepatitis virus receptor
, murine hepatitis virus receptor
, CD66a antigen
, antigen CD66
, ATP-dependent taurocolate-carrier protein
, C-CAM 105
, CEA-related cell adhesion molecule 1 (bone gamma-carboxyglutamic acid (Gla) protein) (osteocalcin)
, bone gamma-carboxyglutamic acid (Gla) protein
, cell-CAM 105