Human CEACAM-8 / CD66b Protein, His Tag

Proteins and Peptides

貨號 Cat. No.
CE8-H5224
規格 Size
100ug
品牌 Brand
ACROBiosystems
Species
Human
Conjugate
Unconjugated
Expression System
HEK293
Tag
His Tag

Description




Source : 


Human CEACAM-8, His Tag (CE8-H5224) is expressed from human 293 cells (HEK293). It contains AA Gln 35 - Ser 319 (Accession # NP_001807.2).


 

Molecule : CEACAM-8


 

Synonyms : CEACAM8,CD66b,CD67,CGM6,NCA-95


 

Format : Powder


 

Category : Bio-Markers & CD Antigens


 

Accession : NP_001807.2


 

Storage : -20℃


 

Shipping condition : Powder,RT


 

Molecular Weight : 32.2 kDa


 

Characteristics :


This protein carries a polyhistidine tag at the C-terminus. The protein has a calculated MW of 32.2 kDa. The protein migrates as 53-66 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.


 

Endotoxin Level : Less than 1.0 EU per μg by the LAL method.


 

Buffer : PBS, pH7.4


 

Description :


Carcinoembryonic antigen-related cell adhesion molecule 8 (CEACAM8) is also known as CD66b (Cluster of Differentiation 66b), CD66b, CD67, CGM6, NCA-95, and is one of seven human CEACAM family members within the immunoglobulin superfamily. CEACAM family members are a set of widely expressed proteins involved in several biological functions, including cell adhesion, migration, signal transduction, and the regulation of gene expression. Abnormal overexpression and downregulation of some CEACAMs have been described in tumor cells. In humans, CEACAMs include type I transmembrane proteins (CEACAM1, CEACAM3, and CEACAM4) and GPI-linked molecules (CEACAM5 through CEACAM8). There is no human CEACAM2. CEACAM8 is a single chain, two Ig-like C2-type (immunoglobulin-like) domains and one Ig-like V-type (immunoglobulin-like) domain. It is an activation marker for human granulocytes.


 

References :


(1) Oikawa,S. et al., 2000, Biochem Biophys Res Commun  278 (3):564-8.
(2) Lasa,A. et al., 2008, Ann Hematol  87 (3):205-11.
(3) Ramachandran P, et al., 2006, J. Proteome Res. 5 (6): 1493–503.
(4) Zhao L, et al., 2002, J. Immunol. Methods 270 (1): 27–35.





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