CEACAM5 (CEACAM1/5) Mouse Monoclonal Antibody [Clone ID: 4/3/17]
CAT#: DM1228
CEACAM5 (CEACAM1/5) mouse monoclonal antibody, clone 4/3/17, Purified
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CNY 5,660.00
货期*
5周
规格
Cited in 7 publications. |
Specifications
Product Data | |
Clone Name | 4/3/17 |
Applications | ELISA, FC, IF, IHC, WB |
Recommend Dilution | ELISA: 1/200-1/400. Cell based ELISA with intakt, transiently transfected cells: 1/200-1/400. Flow Cytometry: 1.2 µg/106 cells. Immunohistochemistry on Cryosections: 1-2 µg/106 cells. |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Immunisation with extracted protein of CEACAM5. |
Specificity | Recognizes CEACAM1, 5 (BGP, CEA, CD66a/e). |
Formulation | PBS, pH 7.2 State: Purified State: Liquid purified IgG fraction |
Concentration | lot specific |
Purification | Affinity Chromatography on Protein G |
Conjugation | Unconjugated |
Storage Condition | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | carcinoembryonic antigen related cell adhesion molecule 5 |
Database Link | |
Background | CEA-related cell adhesion molecules (CEACAM) belong to the carcinoembryonic antigen (CEA) family (1). It consists of seven CEACAM (CEACAM1, CEACAM3-CEACAM8) and 11 pregnancy-specific glycoprotein (PSG1-PSG11) members. The CEA family proteins belong to the immuno-globulin (Ig) superfamily and are composed of one Ig variable-like (IgV) and a varying number (0-6) of Ig constant-like (IgC) domains. CEACAM molecules are membrane-bound either via a transmembrane domain or a glycosyl phosphatidyl inositol (GPI) anchor. CEACAM molecules are differentially expressed in epithelial cells or in leucocytes. Over-expression of CEA/CEACAM5 in tumors of epithelial origin is the basis of its wide-spread use as a tumor marker (2). CEACAM1 expression is down-regulated in many tumors indicating a tumor-suppressive function. The anti-tumor effect may be due to inhibition of tumor angiogenesis, possibly by increased secretion of anti-angiogenic molecules from the cells (3). The function of CEA family members varies widely: they function as cell adhesion molecules, tumor suppressors, regulators of lymphocyte and dendritic cell activation, receptors of Neisseria species and other bacteria (1). |
Synonyms | Carcinoembryonic antigen, BGP, CEA, CEACAM1, CEACAM5, CD66a,e |
Reference Data |
Citations (7)
The use of this Antibodies has been cited in the following citations: |
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Characterization of gastric adenocarcinoma cell lines established from CEA424/SV40 T antigen-transgenic mice with or without a human CEA transgene
,Nvckel J, van den Engel NK, Winter H, Hatz RA, Zimmermann W, Kammerer R,
BMC Cancer
,PubMed ID 16536871
[CEACAM5]
|
Neisseria meningitidis has two independent modes of recognizing its human receptor CEACAM1
,Kuespert K, Roth A, Hauck CR,
PLoS ONE
,PubMed ID 21298042
[CEACAM5]
|
Establishment and phenotypic characterization of human U937 cells with inducible P210 BCR/ABL expression reveals upregulation of CEACAM1 (CD66a)
,Hekansson P, Lassen C, Olofsson T, Baldetorp B, Karlsson A, Gullberg U, Fioretos T,
Leukemia
,PubMed ID 14712293
[CEACAM5]
|
Expression of indoleamine 2,3-dioxygenase in tumor endothelial cells correlates with long-term survival of patients with renal cell carcinoma
,Riesenberg R, Weiler C, Spring O, Eder M, Buchner A, Popp T, Castro M, Kammerer R, Takikawa O, Hatz RA, Stief CG, Hofstetter A, Zimmermann W,
Clin. Cancer Res.
,PubMed ID 18056175
[CEACAM5]
|
CEACAM1 functionally interacts with filamin A and exerts a dual role in the regulation of cell migration
,Klaile E, M|ller MM, Kannicht C, Singer BB, Lucka L,
J. Cell. Sci.
,PubMed ID 16291724
[CEACAM5]
|
Lymphatic reprogramming of microvascular endothelial cells by CEA-related cell adhesion molecule-1 via interaction with VEGFR-3 and Prox1
,Kilic N, Oliveira-Ferrer L, Neshat-Vahid S, Irmak S, Obst-Pernberg K, Wurmbach JH, Loges S, Kilic E, Weil J, Lauke H, Tilki D, Singer BB, Erg|n S,
Blood
,PubMed ID 17761831
[CEACAM5]
|
Homophilic adhesion of human CEACAM1 involves N-terminal domain interactions: structural analysis of the binding site
,Watt SM, Teixeira AM, Zhou GQ, Doyonnas R, Zhang Y, Grunert F, Blumberg RS, Kuroki M, Skubitz KM, Bates PA,
Blood
,PubMed ID 11520797
[CEACAM5]
|
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