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Rat CEACAM1 / CD66a Protein (His Tag) PDF Download

Catalog Size (Price) Quantity In Stock Operation Other Information
80224-R08H
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Protein Production & Purification Service

Carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein) Protein Datasheet

 

CEACAM1 / CD66a Protein Price Inquiry ( Available Sizes )

CEACAM1 / CD66a Protein Product Information

Synonym : CEACAM1
Protein Construction:

A DNA sequence encoding the rat CEACAM1(Met1-Ser422) was expressed with a polyhistidine tag at the C-terminus.

Source: Rat
Expression Host: Human Cells

CEACAM1 / CD66a Protein QC Testing

Purity: > 95 % as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

CEACAM1 / CD66a protein

Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method
Stability: Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal: Gln 35
Molecular Mass:

The recombinant rat CEACAM1 comprises 399 amino acids and predicts a molecular mass of 44.9 kDa. The apparent molecular mass of  the recombinant protein is approximately 66-76 kDa in SDS-PAGE under reducing conditions due to glycosylation.

Formulation: Lyophilized from sterile PBS, pH 7.4.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
  2. Please contact us for any concerns or special requirements.

CEACAM1 / CD66a Protein Usage Guide

Storage: Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

CEACAM1 / CD66a Protein Related Products & Topics

Related Areas:

Cardiovascular>>Angiogenesis>>Adhesion Molecules in Angiogenesis>>CEACAM1/CD66a

Cancer>>Angiogenesis>>Adhesion Molecules in Angiogenesis>>CEACAM1/CD66a

Cancer>>Cancer Biomarkers>>CEACAM1/CD66a

Immunology>>Adhesion Molecule>> Cell Adhesion Molecule (IgSF CAM) >>CEACAM1/CD66a

Immunology>>Cluster of Differentiation>>Granulocyte CD Antigen>>Granulocyte Markers>>CEACAM1/CD66a

Proteins:

Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
CEACAM1/CD66a Human CEACAM1/CD66a Protein, Recombinant 10822-H08H
CEACAM1/CD66a Mouse CEACAM1/CD66a Protein, Recombinant 50571-M08H
CEACAM1/CD66a Rat CEACAM1 / CD66a Protein, Recombinant 80224-R08H

Antibodies:

Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
CEACAM1/CD66a
WB, ELISA, IHC Mouse Monocolonal Antibody 10822-MM02
Human
CEACAM1/CD66a
ELISA Rabbit Polycolonal Antibody 10822-RP01
Human
CEACAM1/CD66a
WB, ELISA Rabbit Polyclonal Antibody (Antigen Affinity Purified) 10822-RP04
Human
CEACAM1/CD66a
WB, ELISA Rabbit Monoclonal Antibody 10822-R006
Mouse
CEACAM1/CD66a
WB, ELISA CEACAM1 / CD66a Antibody 50571-RP01
Mouse
CEACAM1/CD66a
WB, ELISA CEACAM1 / CD66a Antibody (Antigen Affinity Purified) 50571-RP02

CEACAM1 / CD66a Protein Description

Carcinoembryonic antigen (CEA)-related cell adhesion molecule 1 (CEACAM1), also known as biliary glycoprotein I (BGP I) and CD66a, is a member of the carcinoembryonic antigen (CEA) gene family which belongs to the immunoglobulin superfamily. There are two subgroups of the CEA family, the CEA cell adhesion molecules and the pregnancy-specific glycoproteins, and seven CEACAM has been identified in humans including type I  transmembrane proteins (CEACAM-1, CEACAM-3, CEACAM-4) and GPI-linked molecules (CEACAM-5, CEACAM-8). The highly glycosylated CEACAM1 contains one N-terminal V-type I g-like domain and three C2-type I g-like domains within its ECD, and one ITIM motif and a calmodulin binding site in the cytoplasmic region. It was described as an adhesion molecule mediating cell adhesion via both homophilic and heterophilic manners, and was detected on leukocytes, epithelia, and endothelia. Studies have revealed that CEACAM1 performs actions in multiple cellular processes including tissue differentiation, angiogenesis, apoptosis, metastasis, as well as the modulation of innate and adaptive immune responses.

References

  1. Hinoda Y. et al., 1988, Proc Natl Acad Sci. 85: 6959-63.
  2. Zalzali H. et al., 2008, Oncogene. 27: 7131-8.
  3. Erqun S. et al., 2000, Mol Cell. 5: 311-20.
  4. Oliveira-Ferrer L. et al., 2004, Cancer Res. 64: 8932-8.